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Sample records for alloy dissolver solution

  1. METHOD OF DISSOLVING REFRACTORY ALLOYS

    DOEpatents

    Helton, D.M.; Savolainen, J.K.

    1963-04-23

    This patent relates to the dissolution of alloys of uranium with zirconium, thorium, molybdenum, or niobium. The alloy is contacted with an anhydrous solution of mercuric chloride in a low-molecular-weight monohydric alcohol to produce a mercury-containing alcohol slurry. The slurry is then converted to an aqueous system by adding water and driving off the alcohol. The resulting aqueous slurry is electrolyzed in the presence of a mercury cathode to remove the mercury and produce a uranium-bearing aqueous solution. This process is useful for dissolving irradiated nuclear reactor fuels for radiochemical reprocessing by solvent extraction. In addition, zirconium-alloy cladding is selectively removed from uranium dioxide fuel compacts by this means. (AEC)

  2. Chloride removal from plutonium-aluminum alloy dissolver solution prior to purex solvent extraction

    SciTech Connect

    Holcomb, H.P.

    1990-01-01

    The Savannah River Plant (SRP), operated by E. I. du Pont de Nemours Co. for the United States Department of Energy, has successfully recovered plutonium from plutonium-aluminum alloy processed through the F-Canyon Separations facility. The alloy, produced at the Rocky Flats Plant, results from recovery of plutonium residues from spent chloride salts from pyrochemical processing. The alloy, termed scrub alloy'' or Rocky Flats scrub alloy'' (RFSA), contains up to 15 weight percent chloride impurity prior to mercuric ion catalyzed dissolution with fluoride-containing nitric acid. Solutions containing 850 to 3000 {mu}g/mL (parts per million) of chloride result. During subsequent Purex solvent extraction of this solution with 30% tri-n-butyl phosphate in normal paraffin diluent, chloride is rejected to the aqueous waste stream. This stream is eventually evaporated for waste treatment and acid recovery. Chloride concentrations in the product streams, subject to further processing, must be less than 100 {mu}g/mL to prevent excessive corrosion of equipment. This paper describes scrub alloy production at RFP, its dissolution and head end treatment to remove chloride, chloride values in subsequent processing streams including environmental discharges, and the turbidimetric analysis technique. 2 tabs.

  3. PROCESS OF DISSOLVING ZIRCONIUM ALLOYS

    DOEpatents

    Shor, R.S.; Vogler, S.

    1958-01-21

    A process is described for dissolving binary zirconium-uranium alloys where the uranium content is about 2%. In prior dissolution procedures for these alloys, an oxidizing agent was added to prevent the precipitation of uranium tetrafluoride. In the present method complete dissolution is accomplished without the use of the oxidizing agent by using only the stoichiometric amount or slight excess of HF required by the zirconium. The concentration of the acid may range from 2M to 10M and the dissolution is advatageously carried out at a temperature of 80 deg C.

  4. Alloy solution hardening with solute pairs

    DOEpatents

    Mitchell, John W.

    1976-08-24

    Solution hardened alloys are formed by using at least two solutes which form associated solute pairs in the solvent metal lattice. Copper containing equal atomic percentages of aluminum and palladium is an example.

  5. Tungsten solution kinetics and amorphization of nickel in mechanically alloyed Ni-W alloys

    NASA Technical Reports Server (NTRS)

    Aning, A. O.; Wang, Z.; Courtney, T. H.

    1993-01-01

    The kinetics of solution of W, and the subsequent amorphization of Ni, in mechanically alloyed Ni-W alloys has been investigated. As W is a highly abrasive material in the energy intensive devices used for mechanical alloying, we studied the above reactions in different mills. One used hardened steel balls as the grinding media, and the other Al2O3. Abrasion is common to both mills, but Fe wear debris from the hardened steel enters into solution in the Ni rich phases whereas Al2O3 debris is present as small dispersoids. The kinetics of W solution and those of subsequent amorphization do not appear strongly affected by the Fe in solution or the Al2O3 dispersoid. Tungsten dissolves in crystalline Ni in amounts in excess of the equilibrium solubility during alloying. Amorphization of the Ni phase occurs if the W content in this phase exceeds ca. 28 at. pct.

  6. Tungsten solution kinetics and amorphization of nickel in mechanically alloyed Ni-W alloys

    NASA Technical Reports Server (NTRS)

    Aning, A. O.; Wang, Z.; Courtney, T. H.

    1993-01-01

    The kinetics of solution of W, and the subsequent amorphization of Ni, in mechanically alloyed Ni-W alloys has been investigated. As W is a highly abrasive material in the energy intensive devices used for mechanical alloying, we studied the above reactions in different mills. One used hardened steel balls as the grinding media, and the other Al2O3. Abrasion is common to both mills, but Fe wear debris from the hardened steel enters into solution in the Ni rich phases whereas Al2O3 debris is present as small dispersoids. The kinetics of W solution and those of subsequent amorphization do not appear strongly affected by the Fe in solution or the Al2O3 dispersoid. Tungsten dissolves in crystalline Ni in amounts in excess of the equilibrium solubility during alloying. Amorphization of the Ni phase occurs if the W content in this phase exceeds ca. 28 at. pct.

  7. Solution for Depositing an Electroless Cobalt Alloy.

    DTIC Science & Technology

    SOLUTIONS(MIXTURES), *ELECTROLESS PLATING), (*PATENTS, ELECTROLESS PLATING), (*COBALT ALLOYS, ELECTROLESS PLATING), ADDITIVES, SODIUM COMPOUNDS... TUNGSTATES , POTASSIUM COMPOUNDS, NICKEL COMPOUNDS, SULFATES, THIOUREA, MAGNETIC PROPERTIES

  8. A review of the effects of dissolved ozone on the corrosion behavior of metals and alloys

    SciTech Connect

    Brown, B.E.; Duquette, D.J.

    1994-12-31

    Ozone is currently being considered as a possible replacement for chlorine based compounds as a biocide. Yet, a review of current literature related to the corrosion behavior of metals and alloys exposed to ozonated solutions indicates that there is considerable confusion concerning the effects of this strong oxidant. Some studies indicate that dissolved ozone will increase the corrosion rates of alloys such as carbon steel or brasses when compared to aerated solutions. Others indicate a beneficial effect of ozone, while still others indicate a neutral effect. Virtually all of these reports are for fresh waters, few relate to localized corrosion behavior, and most are anecdotal in that they report observations from service conditions with poorly defined variables. This review attempts to summarize the various corrosion rates reported in the literature, as well as present data obtained in laboratory studies of metals exposed to ozone in chloride containing environments, including artificial sea water. 28 refs.

  9. Neptunium estimation in dissolver and high-level-waste solutions

    SciTech Connect

    Pathak, P.N.; Prabhu, D.R.; Kanekar, A.S.; Manchanda, V.K.

    2008-07-01

    This papers deals with the optimization of the experimental conditions for the estimation of {sup 237}Np in spent-fuel dissolver/high-level waste solutions using thenoyltrifluoroacetone as the extractant. (authors)

  10. Chloride Analysis of RFSA Second Campaign Dissolver Solution

    SciTech Connect

    Holcomb, H.P.

    2001-05-17

    The dissolver solution from the second RFSA campaign was analyzed for chloride using the recently-developed turbidimetric method. Prior to chloride removal in head end, the solution contained 1625 ppm chloride. After chloride removal with Hg(I) and prior to feeding to solvent extraction, the solution contained only 75 ppm chloride. This report discusses those analysis results.

  11. Solution Potentials Indicate Aluminum-Alloy Tempers

    NASA Technical Reports Server (NTRS)

    Danford, M. D.

    1985-01-01

    Report discusses use of solution potential as measure of temper of aluminum alloys. Technique based on fact that different tempers or heat treatments exhibit different solution potentials as function of aging time.

  12. Alloy softening in binary iron solid solutions

    NASA Technical Reports Server (NTRS)

    Stephens, J. R.; Witzke, W. R.

    1976-01-01

    An investigation was conducted to determine softening and hardening behavior in 19 binary iron-alloy systems. Microhardness tests were conducted at four temperatures in the range 77 to 411 K. Alloy softening was exhibited by 17 of the 19 alloy systems. Alloy softening observed in 15 of the alloy systems was attributed to an intrinsic mechanism, believed to be lowering of the Peierls (lattice friction) stress. Softening and hardening rates could be correlated with the atomic radius ratio of solute to iron. Softening observed in two other systems was attributed to an extrinsic mechanism, believed to be associated with scavenging of interstitial impurities.

  13. Alloy softening in binary iron solid solutions

    NASA Technical Reports Server (NTRS)

    Stephens, J. R.; Witzke, W. R.

    1976-01-01

    An experimental study was conducted to determine whether alloy softening in Fe alloys is dependent on electron concentration and to provide a direct comparison of alloy softening and hardening in several binary Fe alloy systems having the same processing history. Alloy additions to Fe included the elements in the Periods 4-6 and the Groups IV-VIII with the exception of technetium. A total of 19 alloy systems was investigated, and hardness testing was the primary means of evaluation. Testing was carried out at four temperatures over a homologous temperature range of 0.043-0.227 times the absolute melting temperature of unalloyed Fe. Major conclusions are that the atomic radius ratio of solute-to-Fe is the key factor in controlling low-temperature hardness of the binary Fe alloys and that alloy softening rates at 77 K and alloy hardening rates at 411 K are correlated with this atomic radius ratio for 15 of the binary alloy systems. Mechanisms of alloy softening and hardening are proposed.

  14. Thermodynamic properties of gases dissolved in electrolyte solutions.

    NASA Technical Reports Server (NTRS)

    Tiepel, E. W.; Gubbins, K. E.

    1973-01-01

    A method based on perturbation theory for mixtures is applied to the prediction of thermodynamic properties of gases dissolved in electrolyte solutions. The theory is compared with experimental data for the dependence of the solute activity coefficient on concentration, temperature, and pressure; calculations are included for partial molal enthalpy and volume of the dissolved gas. The theory is also compared with previous theories for salt effects and found to be superior. The calculations are best for salting-out systems. The qualitative feature of salting-in is predicted by the theory, but quantitative predictions are not satisfactory for such systems; this is attributed to approximations made in evaluating the perturbation terms.

  15. Thermodynamic properties of gases dissolved in electrolyte solutions.

    NASA Technical Reports Server (NTRS)

    Tiepel, E. W.; Gubbins, K. E.

    1973-01-01

    A method based on perturbation theory for mixtures is applied to the prediction of thermodynamic properties of gases dissolved in electrolyte solutions. The theory is compared with experimental data for the dependence of the solute activity coefficient on concentration, temperature, and pressure; calculations are included for partial molal enthalpy and volume of the dissolved gas. The theory is also compared with previous theories for salt effects and found to be superior. The calculations are best for salting-out systems. The qualitative feature of salting-in is predicted by the theory, but quantitative predictions are not satisfactory for such systems; this is attributed to approximations made in evaluating the perturbation terms.

  16. Corrosion behavior of Ti-Ag alloys used in dentistry in lactic acid solution

    NASA Astrophysics Data System (ADS)

    Takahashi, Masatoshi; Kikuchi, Masafumi; Takada, Yukyo

    2011-02-01

    The purpose of this study was to evaluate the corrosion resistance of experimental Ti-Ag alloys used as dental materials. An elution test and a rest-potential measurement of alloys with 5-30 mass.% Ag were performed in a 1 % lactic acid solution. The amount of Ti ions released from the α phase of the Ti-Ag alloys decreased as the Ag concentration increased. TiAg present in the alloys dissolved preferentially, but Ti2Ag did not. The rest potentials of the Ti-Ag alloys were significantly higher than that of pure titanium. The elution test and the rest-potential measurement revealed that the Ti-Ag alloys, which formed a single α-titanium structure or contained a titanium and Ti2Ag, had excellent corrosion resistance that was comparable or superior to that of pure titanium.

  17. PROCESS FOR DISSOLVING BINARY URANIUM-ZIRCONIUM OR ZIRCONIUM-BASE ALLOYS

    DOEpatents

    Jonke, A.A.; Barghusen, J.J.; Levitz, N.M.

    1962-08-14

    A process of dissolving uranium-- zirconium and zircaloy alloys, e.g. jackets of fuel elements, with an anhydrous hydrogen fluoride containing from 10 to 32% by weight of hydrogen chloride at between 400 and 450 deg C., preferably while in contact with a fluidized inert powder, such as calcium fluoride is described. (AEC)

  18. Deformation and fracture of aluminum-lithium alloys: The effect of dissolved hydrogen

    NASA Technical Reports Server (NTRS)

    Rivet, F. C.; Swanson, R. E.

    1990-01-01

    The effects of dissolved hydrogen on the mechanical properties of 2090 and 2219 alloys are studied. The work done during this semi-annual period consists of the hydrogen charging study and some preliminary mechanical tests. Prior to SIMS analysis, several potentiostatic and galvanostatic experiments were performed for various times (going from 10 minutes to several hours) in the cathodic zone, and for the two aqueous solutions: 0.04N of HCl and 0.1N NaOH both combined with a small amount of As2O3. A study of the surface damage was conducted in parallel with the charging experiments. Those tests were performed to choose the best charging conditions without surface damage. Disk rupture tests and tensile tests are part of the study designed to investigate the effect of temperature, surface roughness, strain rate, and environment on the fracture behavior. The importance of the roughness and environment were shown using the disk rupture test as well as the importance of the strain rate under hydrogen environment. The tensile tests, without hydrogen effects, have not shown significant differences between low and room temperature.

  19. Alloying Solid Solution Strengthening of Fe-Ga Alloys: A First-Principle Study

    DTIC Science & Technology

    2006-01-01

    effect from alloying additions of Nb, Mo, V, Cr and Co in cubic solid solution of Fe-Ga alloys. Mayer bond order "BO" values were used to evaluate the...that transition metal Nb achieves the best strengthening effect in Fe-Ga alloys. The solid solution strengthening follows a trend from larger to

  20. Magnetic Damping of Solid Solution Semiconductor Alloys

    NASA Technical Reports Server (NTRS)

    Szofran, Frank R.; Benz, K. W.; Croell, Arne; Dold, Peter; Cobb, Sharon D.; Volz, Martin P.; Motakef, Shariar

    1999-01-01

    The objective of this study is to: (1) experimentally test the validity of the modeling predictions applicable to the magnetic damping of convective flows in electrically conductive melts as this applies to the bulk growth of solid solution semiconducting materials; and (2) assess the effectiveness of steady magnetic fields in reducing the fluid flows occurring in these materials during processing. To achieve the objectives of this investigation, we are carrying out a comprehensive program in the Bridgman and floating-zone configurations using the solid solution alloy system Ge-Si. This alloy system has been studied extensively in environments that have not simultaneously included both low gravity and an applied magnetic field. Also, all compositions have a high electrical conductivity, and the materials parameters permit reasonable growth rates. An important supporting investigation is determining the role, if any, that thermoelectromagnetic convection (TEMC) plays during growth of these materials in a magnetic field. TEMC has significant implications for the deployment of a Magnetic Damping Furnace in space. This effect will be especially important in solid solutions where the growth interface is, in general, neither isothermal nor isoconcentrational. It could be important in single melting point materials, also, if faceting takes place producing a non-isothermal interface. In conclusion, magnetic fields up to 5 Tesla are sufficient to eliminate time-dependent convection in silicon floating zones and possibly Bridgman growth of Ge-Si alloys. In both cases, steady convection appears to be more significant for mass transport than diffusion, even at 5 Tesla in the geometries used here. These results are corroborated in both growth configurations by calculations.

  1. Magnetic Damping of Solid Solution Semiconductor Alloys

    NASA Technical Reports Server (NTRS)

    Szofran, Frank R.; Benz, K. W.; Corell, Arne; Dold, Peter; Cobb, Sharon D.; Volz, Martin P.; Motakef, Shariar

    1998-01-01

    The objective of this study is to conduct the Earth-based research sufficient to successfully propose a flight experiment (1) to experimentally test the validity of the modeling predictions applicable to the magnetic damping of convective flows in conductive melts as this applies to the bulk growth of solid solution semiconducting materials in the reduced gravitational levels available in low Earth orbit and (2) to assess the effectiveness of steady magnetic fields in reducing the fluid flows occurring in these materials during space processing. To achieve the objectives of this investigation, we are carrying out a comprehensive program in the Bridgman and floating-zone configurations using the solid solution alloy system Ge-Si. This alloy system was chosen because it has been studied extensively in environments that have not simultaneously included both low gravity and an applied magnetic field. Also, all compositions have a high electrical conductivity, and the materials parameters permit high growth rates compared to many other commonly studied alloy semiconductors. An important supporting investigation is determining the role, if any, that thermoelectromagnetic convection (TEMC) plays during growth of these materials in a magnetic field. Some compositional anomalies observed by us in magnetic grown crystals can only be explained by TEMC; this has significant implications for the deployment of a Magnetic Damping Furnace in space. This effect will be especially important in solid solutions where the growth interface is, in general, neither isothermal nor isoconcentrational. It could be important in single melting point materials, also, if faceting takes place producing a non-isothermal interface.

  2. Discoloration of titanium alloy in acidic saline solutions with peroxide.

    PubMed

    Takemoto, Shinji; Hattori, Masayuki; Yoshinari, Masao; Kawada, Eiji; Oda, Yutaka

    2013-01-01

    The objective of this study was to compare corrosion behavior in several titanium alloys with immersion in acidulated saline solutions containing hydrogen peroxide. Seven types of titanium alloy were immersed in saline solutions with varying levels of pH and hydrogen peroxide content, and resulting differences in color and release of metallic elements determined in each alloy. Some alloys were characterized using Auger electron spectroscopy. Ti-55Ni alloy showed a high level of dissolution and difference in color. With immersion in solution containing hydrogen peroxide at pH 4, the other alloys showed a marked difference in color but a low level of dissolution. The formation of a thick oxide film was observed in commercially pure titanium showing discoloration. The results suggest that discoloration in titanium alloys immersed in hydrogen peroxide-containing acidulated solutions is caused by an increase in the thickness of this oxide film, whereas discoloration of Ti-55Ni is caused by corrosion.

  3. Effects of fluoride and dissolved oxygen concentrations on the corrosion behavior of pure titanium and titanium alloys.

    PubMed

    Nakagawa, Masaharu; Matsuya, Shigeki; Udoh, Koichi

    2002-06-01

    The effects of dissolved-oxygen concentration and fluoride concentration on the corrosion behaviors of commercial pure titanium, Ti-6Al-4V and Ti-6Al-7Nb alloys and experimentally produced Ti-0.2Pd and Ti-0.5Pt alloys were examined using the corrosion potential measurements. The amount of dissolved Ti was analyzed by inductively coupled plasma mass spectroscopy. A decrease in the dissolved-oxygen concentration tended to reduce the corrosion resistance of Ti and Ti alloys. If there was no fluoride, however, corrosion did not occur. Under low dissolved-oxygen conditions, the corrosion of pure Ti and Ti-6Al-4V and Ti-6Al-7Nb alloys might easily take place in the presence of small amounts of fluoride. They were corroded by half or less of the fluoride concentrations in commercial dentifrices. The Ti-0.2Pd and Ti-0.5Pt alloys did not corrode more, even under the low dissolved-oxygen conditions and a fluoride-containing environment, than pure Ti and Ti-6Al-4V and Ti-6Al-7Nb alloys. These alloys are expected to be useful as new Ti alloys with high corrosion resistance in dental use.

  4. Impact of solute concentration on the electrocatalytic conversion of dissolved gases in buffered solutions

    NASA Astrophysics Data System (ADS)

    Shinagawa, Tatsuya; Takanabe, Kazuhiro

    2015-08-01

    To maintain local pH levels near the electrode during electrochemical reactions, the use of buffer solutions is effective. Nevertheless, the critical effects of the buffer concentration on electrocatalytic performances have not been discussed in detail. In this study, two fundamental electrochemical reactions, oxygen reduction reaction (ORR) and hydrogen oxidation reaction (HOR), on a platinum rotating disk electrode are chosen as model gas-related aqueous electrochemical reactions at various phosphate concentrations. Our detailed investigations revealed that the kinetic and limiting diffusion current densities for both the ORR and HOR logarithmically decrease with increasing solute concentration (log |jORR | = - 0.39 c + 0.92 , log |jHOR | = - 0.35 c + 0.73) . To clarify the physical aspects of this phenomenon, the electrolyte characteristics are addressed: with increasing phosphate concentration, the gas solubility decrease, the kinematic viscosity of the solution increase and the diffusion coefficient of the dissolved gases decrease. The simulated limiting diffusion currents using the aforementioned parameters match the measured ones very well (log |jORR | = - 0.43 c + 0.99 , log |jHOR | = - 0.40 c + 0.54) , accurately describing the consequences of the electrolyte concentration. These alterations of the electrolyte properties associated with the solute concentration are universally applicable to other aqueous gas-related electrochemical reactions because the currents are purely determined by mass transfer of the dissolved gases.

  5. Corrosion behavior of pure titanium and titanium alloys in various concentrations of Acidulated Phosphate Fluoride (APF) solutions.

    PubMed

    Matono, Yoshinari; Nakagawa, Masaharu; Matsuya, Shigeki; Ishikawa, Kunio; Terada, Yoshihiro

    2006-03-01

    The corrosion behaviors of Ti, Ti-6Al-7Nb and Ti-6Al-4V alloys, and an experimentally produced Ti-0.5Pt alloy in 0.05% to 2.0% concentrations of Acidulated Phosphate Fluoride (APF) solutions (corresponding to 226 to 9,050 ppm fluoride at pH 3.5 or 3.6) were examined. While the corrosion of Ti, Ti-6Al-7Nb and Ti-6Al-4V alloys might occur easily even in a diluted 0.05% APF solution, dissolution of Ti from the Ti-0.5Pt alloy was observed only in test solutions with APF concentration exceeding 0.2%. When Ti-6Al-7Nb and Ti-6Al-4V alloys were immersed in 2.0% APF solution, their surfaces were entirely covered by compact corrosion products of Na3TiF6 due to severe corrosion. As a result, Ti dissolution was prevented and the amount of Ti dissolved decreased. However, since Ti was covered by porous, large-sized corrosion products of Na3TiF6 and that Ti-0.5Pt alloy was not covered with any corrosion product, the amount of Ti dissolved increased in the 2.0% APF solution.

  6. Summary of Tests to Determine Effectiveness of Gelatin Strike on SS{ampersand}C Dissolver Solutions

    SciTech Connect

    Murray, A.M.; Karraker, D.G.

    1998-05-01

    The solutions from the dissolution of sand, slag, and crucible (SS&C) material are sufficiently different from previous solutions processed via the F-Canyon Purex process that the effectiveness of individual process steps needed to be ascertained. In this study, the effectiveness of gelatin strike was tested under a variety of conditions. Specifically, several concentrations of silica, fluoride, nitric acid (HNO{sub 3}), boric acid (H{sub 3}BO{sub 3}), and aluminium nitrate nonahydrate (ANN) were studied. The disengagement times of surrogate and plant SS&C dissolver solutions from plant solvent also were measured. The results of the tests indicate that gelatin strike does not coagulate the silica at the low concentration of silica ({tilde 30} ppm) expected in the SS&C dissolver solutions because the silicon is complexed with fluoride ions (e.g., SiF{sub 6}{sup -2}). The silicon fluoride complex is expected to remain with the aqueous phase during solvent extraction. The disengagement times of the dissolver solutions from the plant solvent were not affected by the presence of low concentrations of silica and no third phase formation was observed in the disengagement phase with the low silica concentrations. Tests of surrogate SS&C dissolver solutions with higher concentration of silica (less than 150 ppm) did show that gelatin strike followed by centrifugation resulted in good phase disengagement of the surrogate SS{ampersand}C dissolver solution from the plant dissolver solution. At the higher silica concentrations, there is not sufficient fluoride to complex with the silica, and the silica must be entrained by the gelatin and removed from the dissolver solution prior to solvent extraction.

  7. Suppression of vacancy cluster growth in concentrated solid solution alloys

    SciTech Connect

    Zhao, Shijun; Velisa, Gihan; Xue, Haizhou; Bei, Hongbin; Weber, William J.; Zhang, Yanwen

    2016-12-13

    Large vacancy clusters, such as stacking-fault tetrahedra, are detrimental vacancy-type defects in ion-irradiated structural alloys. Suppression of vacancy cluster formation and growth is highly desirable to improve the irradiation tolerance of these materials. In this paper, we demonstrate that vacancy cluster growth can be inhibited in concentrated solid solution alloys by modifying cluster migration pathways and diffusion kinetics. The alloying effects of Fe and Cr on the migration of vacancy clusters in Ni concentrated alloys are investigated by molecular dynamics simulations and ion irradiation experiment. While the diffusion coefficients of small vacancy clusters in Ni-based binary and ternary solid solution alloys are higher than in pure Ni, they become lower for large clusters. This observation suggests that large clusters can easily migrate and grow to very large sizes in pure Ni. In contrast, cluster growth is suppressed in solid solution alloys owing to the limited mobility of large vacancy clusters. Finally, the differences in cluster sizes and mobilities in Ni and in solid solution alloys are consistent with the results from ion irradiation experiments.

  8. Solid solution lithium alloy cermet anodes

    SciTech Connect

    Richardson, Thomas J.

    2013-07-09

    A metal-ceramic composite ("cermet") has been produced by a chemical reaction between a lithium compound and another metal. The cermet has advantageous physical properties, high surface area relative to lithium metal or its alloys, and is easily formed into a desired shape. An example is the formation of a lithium-magnesium nitride cermet by reaction of lithium nitride with magnesium. The reaction results in magnesium nitride grains coated with a layer of lithium. The nitride is inert when used in a battery. It supports the metal in a high surface area form, while stabilizing the electrode with respect to dendrite formation. By using an excess of magnesium metal in the reaction process, a cermet of magnesium nitride is produced, coated with a lithium-magnesium alloy of any desired composition. This alloy inhibits dendrite formation by causing lithium deposited on its surface to diffuse under a chemical potential into the bulk of the alloy.

  9. Tissue-dissolving capacity and antibacterial effect of buffered and unbuffered hypochlorite solutions.

    PubMed

    Zehnder, Matthias; Kosicki, Daniel; Luder, Hansueli; Sener, Beatrice; Waltimo, Tuomas

    2002-12-01

    The goal of this study was to compare the dissolving potential of Dakin's solution with that of equivalent buffered and unbuffered sodium hypochlorite solutions on fresh and decayed tissues. In addition, the antimicrobial effect of Dakin's solution and equivalent unbuffered hypochlorite was tested. Tissue specimens were obtained from freshly dissected pig palates. Unbuffered 2.5% and 0.5% sodium hypochlorite solutions and 0.5% solutions buffered at a pH of 12 and a pH of 9 (Dakin's solution) were tested on fresh and decayed tissue. Tissue decay was assessed histologically. Antimicrobial testing was performed with Enterococcus faecalis in dentin blocks and on filter papers. The 2.5% NaOCl solution was substantially more effective than the three 0.5% solutions in dissolving the test tissues. Buffering had little effect on tissue dissolution, and Dakin's solution was equally effective on decayed and fresh tissues. No differences were recorded for the antibacterial properties of Dakin's solution and an equivalent unbuffered hypochlorite solution. In contrast to earlier statements, the results of this study do not demonstrate any benefit from buffering sodium hypochlorite with sodium bicarbonate according to Dakin's method. An irrigation solution with less dissolving potential may be obtained by simply diluting stock solutions of NaOCl with water.

  10. The Influence of Dissolved hydrogen on Nickel Alloy SCC: A Window to Fundamental Insight

    SciTech Connect

    D.S. Morton; S.A. Attanasio; G.A. Young; P.L. Andresen; T.M. Angeliu

    2000-10-12

    Prior stress corrosion crack growth rate (SCCGR) testing of nickel alloys as a function of the aqueous hydrogen concentration (i.e., the concentration of hydrogen dissolved in the water) has identified different functionalities at 338 and 360 C. These SCCGR dependencies have been uniquely explained in terms of the stability of nickel oxide. The present work evaluates whether the influence of aqueous hydrogen concentration on SCCGR is fundamentally due to effects on hydrogen absorption and/or corrosion kinetics. Hydrogen permeation tests were conducted to measure hydrogen pickup in and transport through the metal. Repassivation tests were performed in an attempt to quantify the corrosion kinetics. The aqueous hydrogen concentration dependency of these fundamental parameters (hydrogen permeation, repassivation) has been used to qualitatively evaluate the film-rupture/oxidation (FRO) and hydrogen assisted cracking (HAC) SCC mechanisms. This paper discusses the conditions that must be imposed upon these mechanisms to describe the known nickel alloy SCCGR aqueous hydrogen concentration functionality. Specifically, the buildup of hydrogen within Alloy 600 (measured through permeability) does not exhibit the same functionality as SCC with respect to the aqueous hydrogen concentration. This result implies that if HAC is the dominant SCC mechanism, then corrosion at isolated active path regions (i.e., surface initiation sites or cracks) must be the source of localized elevated detrimental hydrogen. Repassivation tests showed little temperature sensitivity over the range of 204 to 360 C. This result implies that for either the FRO or the HAC mechanism, corrosion processes (e.g., at a crack tip, in the crack wake, or on surfaces external to the crack) cannot by themselves explain the strong temperature dependence of nickel alloy SCC.

  11. Corrosion of metastable iron alloys in aqueous solutions

    NASA Astrophysics Data System (ADS)

    Wolf, Gerhard K.; Ferber, H.

    1983-05-01

    There exist some examples showing that metastable surface alloys can modify the corrision properties of a substrate in the same way as stable alloys do. In the present paper the corrosion behaviour of metastable surface alloys obtained by implanting gold, lead and mercury in iron was studied in aqueous solution of pH = 5.6. Potentiodynamic current density-potential curves were recorded of the implanted samples without further treatment and after isothermal annealing to temperatures up to 800°C. The results were compared with structural information on the alloys obtained by Turos et al. with α-backscattering and channeling experiments. Gold implantation turned out to enhance the active corrosion rate of iron, while lead and mercury had an impeding effect. The annealing experiments showed that the surface alloying facilitated the passivation of iron as long as the substitutional solid solution was "(meta)stable". After the breakdown at higher annealing temperatures leading to surface migration and clustering of the implanted elements a significant increase of the critical current density for passivation took place. This indicates passivation difficulties caused by the heterogeneous distribution of the "alloying" particles. In general the results suggest that substitutional metastable iron alloys cause in a systematic way corrosion inhibition or enhancement. However, their corrosion properties may change completely for non-substitutional distribution of the alloying elements as originating from annealing at higher temperatures.

  12. Enhancement of the adhesion between cobalt-base alloys and veneer ceramic by application of an oxide dissolving primer.

    PubMed

    Kohorst, Philipp; Dittmer, Marc Philipp; Stiesch, Meike

    2013-12-01

    Uncontrolled formation of an oxide layer on base metal alloy surface impairs adhesion between the alloy and veneer ceramic. The aim of this study was to investigate the influence of an oxide dissolving primer on the adhesion between cobalt-base alloys and a veneer ceramic. Combinations of two cobalt-base alloys (Bärlight/BL, Cara Process/CP) and one veneering ceramic (HeraCeram) were investigated. 40 rectangular specimens of each alloy were covered with the veneer ceramic; half of the alloy samples were treated with an oxide dissolving primer (NP-Primer) prior to veneering (n=20). Subsequently, the veneering surface was ground flat and notched using the single-edge V-notched-beam method. Then specimens were loaded in a four-point bending test and the critical load to induce stable crack extension at the adhesion interface was determined, in order to calculate the strain energy release rate (G, J/m(2)). Finally, fracture surfaces of the specimens were evaluated by scanning electron microscopy (SEM). Strain energy release rates averaged between 24.1J/m(2) and 28.8 J/m(2). While application of the primer statistically significantly increased adhesion between alloy and ceramic with the BL specimens (p=0.035), no significant influence was found for the CP specimens (p=0.785). For both material combinations, SEM analysis revealed enhanced wetting of the alloy surfaces with ceramic after application of the primer. Application of an oxide dissolving primer increases the wettability of cobalt-base alloy surfaces and thus improves adhesion to veneering ceramics. This may enhance the long-term stability of bilayer restorations made from these materials. Copyright © 2013 Academy of Dental Materials. Published by Elsevier Ltd. All rights reserved.

  13. Suppression of vacancy cluster growth in concentrated solid solution alloys

    DOE PAGES

    Zhao, Shijun; Velisa, Gihan; Xue, Haizhou; ...

    2016-12-13

    Large vacancy clusters, such as stacking-fault tetrahedra, are detrimental vacancy-type defects in ion-irradiated structural alloys. Suppression of vacancy cluster formation and growth is highly desirable to improve the irradiation tolerance of these materials. In this paper, we demonstrate that vacancy cluster growth can be inhibited in concentrated solid solution alloys by modifying cluster migration pathways and diffusion kinetics. The alloying effects of Fe and Cr on the migration of vacancy clusters in Ni concentrated alloys are investigated by molecular dynamics simulations and ion irradiation experiment. While the diffusion coefficients of small vacancy clusters in Ni-based binary and ternary solid solutionmore » alloys are higher than in pure Ni, they become lower for large clusters. This observation suggests that large clusters can easily migrate and grow to very large sizes in pure Ni. In contrast, cluster growth is suppressed in solid solution alloys owing to the limited mobility of large vacancy clusters. Finally, the differences in cluster sizes and mobilities in Ni and in solid solution alloys are consistent with the results from ion irradiation experiments.« less

  14. Iodine evolution from nuclear fuel dissolver solutions by air sparging

    SciTech Connect

    Morgan, J.G.; Holland, W.D.

    1980-01-01

    Iodine removal rates were measured from air-sparged nitric acid solutions in experiments designed to simulate part of the iodine recovery system in an advanced fuel reprocessing flowsheet. Variables studied were temperature, sparge rate, and iodine and acid concentrations. Experimental mass transfer coefficients were determined and compared to results based on correlations available in the literature.

  15. Electrodeposition of cobalt-chromium alloy from trivalent chromium solutions

    SciTech Connect

    Dasarathy, H.; Riley, C.; Coble, H.D. . Dept. of Chemistry and Materials Science)

    1994-07-01

    Cobalt-chromium alloy was deposited from plating solutions containing cobalt(II) chloride and chromium(III) chloride at 3.5 pH. The deposits were obtained using both single and mixed complex solutions. Deposit morphology showed significant dependence on the complexing agent(s) used. Partitioning of the two components in the deposit as determined by energy dispersive spectroscopy depended on plating parameters such as concentration ratio of the two salts in the solution, complexing agent, type of current (both dc and pulsed current were studied), and current density. X-ray photoelectron spectroscopy spectra collected from as-deposited alloy revealed the presence of both oxides and metals. X-ray diffraction spectra for the alloy deposit indicated solid solution formation.

  16. Chemical milling solution reveals stress corrosion cracks in titanium alloy

    NASA Technical Reports Server (NTRS)

    Braski, D. N.

    1967-01-01

    Solution of hydrogen flouride, hydrogen peroxide, and water reveals hot salt stress corrosion cracks in various titanium alloys. After the surface is rinsed in water, dried, and swabbed with the solution, it can be observed by the naked eye or at low magnification.

  17. Shelf life, dissolving action, and antibacterial activity of a neutralized 2.5% sodium hypochlorite solution.

    PubMed

    Camps, Jean; Pommel, Ludovic; Aubut, Virginie; Verhille, Bernard; Satoshi, Fukuzaki; Lascola, Bernad; About, Imad

    2009-08-01

    The aim was to evaluate the shelf life and the dissolving and antibacterial properties of a neutralized 2.5% NaOCl solution. The loss of available chlorine and the pH of the neutralized 2.5% NaOCl solution were recorded to determine its shelf life. The dissolving action on bovine dental pulp was assessed measuring weight loss, pH variation, and decrease in available chlorine content. The antibacterial activity was evaluated on artificially infected human teeth. The roots were endodontically prepared, sterilized, and inoculated with Enterococcus faecalis before irrigation with the neutralized solution. The presence of intracanal bacteria after irrigation was recorded. The neutralized solution presented a shelf life of 2 hours, dissolving capacities equivalent to control for the first 5 minutes, and a better antibacterial efficiency. The neutralized 2.5% NaOCl solution must be used within 2 hours after mixing, should be frequently renewed to maintain its dissolving capacities, and presented enhanced antibacterial properties.

  18. Influence of solid-solution treatment on microstructure, mechanical property and corrosion behavior of biodegradable Mg-Zn-Ca alloy

    NASA Astrophysics Data System (ADS)

    Ly, Xuan Nam; Yang, S.; Qin, Y.

    2017-03-01

    The influence of solid-solution treatment on microstructure, mechanical property and corrosion behavior of Mg-Zn-Ca alloy was studied in the present investigation by SEM, tensile test, electrochemical and immersion test. The results show that the microstructure of Mg alloys after solid solution treatment significantly changed, a large number of the second phase (Ca2Mg6Zn3, Mg2Ca) dissolved into the α-Mg matrix reaching a supersaturated state, and the grains size was bigger than before solid solution treatment; the mechanical properties were obviously improved. In particular the tensile strength of 0.5wt.% Ca of Mg alloy reached 220MPa and the ductility reached 16.6%. Compared with the as-cast Mg alloys, the corrosion potential after solid-solution treatment slightly shifted negative, but the corrosion current density significantly decreased. After solid solution treatment, the surface corrosion was not serious and the result of weight gain was lower compared with those of the as-cast Mg alloys.

  19. Holographic studies of the solution surrounding a growing or dissolving crystal

    NASA Astrophysics Data System (ADS)

    Petrovsky, V. A.; Rakin, V. I.; Ruzov, V. P.

    It is experimentally determined that a solution is "stratified" in the presence of growing or dissolving crystals. It is established that the crystal uses more effectively the "stratified zone" of the whole volume, the concentration in the remaining part of the solution is changing due to diffusion. The time of crystal growth depends on immersion depth. Cubo-octahedral crystals of potassium alum have been chosen as the model material for this investigation.

  20. Solution Treatment Effect on Tensile, Impact and Fracture Behaviour of Trace Zr Added Al-12Si-1Mg-1Cu Piston Alloy

    NASA Astrophysics Data System (ADS)

    Kaiser, Md. Salim

    2017-05-01

    The effects of T6 solution treatment on tensile, impact and fracture properties of cast Al-12Si-1Mg-1Cu piston alloys with trace of zirconium were investigated. Cast alloys were given precipitation strengthening treatment having a sequence of homogenizing, solutionizing, quenching and ageing. Both cast and solutionized samples are isochronally aged for 90 min at different temperatures up to 300 °C. Tensile and impact properties of the differently processed alloys have been studied to understand the precipitation strengthening of the alloys. Fractograpy of the alloys were observed to understand the mode of fracture. It is observed that the improvement in tensile properties in the aged alloys through heat treatment is mainly attributed to the formation of the Al2Cu and Mg2Si precipitates within the Al matrix. Solution treatment improves the tensile strength for the reason that during solution treatment some alloying elements are re-dissolved to produce a solute-rich solid solution. Impact energy decreases with ageing temperature due to formation of GP zones, β' and β precipitates. The fractography shows large and small dimple structure and broken or cracked primary Si, particles. Microstructure study of alloys revealed that the solution treatment improved distribution of silicon grains. The addition of Zr produces an improvement in the tensile properties as a result of its grain refining action and grain coarsening resistance in the matrix at a higher temperature.

  1. Solidification and crystal growth of solid solution semiconducting alloys

    NASA Technical Reports Server (NTRS)

    Lehoczky, S. L.; Szofran, F. R.

    1984-01-01

    Problems associated with the solidification and crytal growth of solid-solution semiconducting alloy crystals in a terrestrial environment are described. A detailed description is given of the results for the growth of mercury cadmium telluride (HgCdTe) alloy crystals by directional solidification, because of their considerable technological importance. A series of HgCdTe alloy crystals are grown from pseudobinary melts by a vertical Bridgman method using a wide range of growth rates and thermal conditions. Precision measurements are performed to establish compositional profiles for the crystals. The compositional variations are related to compositional variations in the melts that can result from two-dimensional diffusion or density gradient driven flow effects ahead of the growth interface. These effects are discussed in terms of the alloy phase equilibrium properties, the recent high temperature thermophysical data for the alloys and the highly unusual heat transfer characteristics of the alloy/ampule/furnace system that may readily lead to double diffusive convective flows in a gravitational environment.

  2. Solidification and crystal growth of solid solution semiconducting alloys

    NASA Technical Reports Server (NTRS)

    Lehoczky, S. L.; Szofran, F. R.

    1984-01-01

    Problems associated with the solidification and crytal growth of solid-solution semiconducting alloy crystals in a terrestrial environment are described. A detailed description is given of the results for the growth of mercury cadmium telluride (HgCdTe) alloy crystals by directional solidification, because of their considerable technological importance. A series of HgCdTe alloy crystals are grown from pseudobinary melts by a vertical Bridgman method using a wide range of growth rates and thermal conditions. Precision measurements are performed to establish compositional profiles for the crystals. The compositional variations are related to compositional variations in the melts that can result from two-dimensional diffusion or density gradient driven flow effects ahead of the growth interface. These effects are discussed in terms of the alloy phase equilibrium properties, the recent high temperature thermophysical data for the alloys and the highly unusual heat transfer characteristics of the alloy/ampule/furnace system that may readily lead to double diffusive convective flows in a gravitational environment.

  3. Corrosion of dental copper, nickel, and gold alloys in artificial saliva and saline solutions.

    PubMed

    Johansson, B I; Lemons, J E; Hao, S Q

    1989-09-01

    The purpose of this investigation was to study the tarnish and corrosion of three commercial copper alloys, three experimental copper alloys, two nickel alloys, and one high-gold alloy by exposing the specimens for four weeks to artificial saliva and saline solutions. Half of the specimens were brushed, and the solutions were changed regularly. The copper-based and the beryllium-containing nickel alloys exhibited significant surface alterations after exposure to either solution. The potential of elevated release of ions to the oral cavity and to the target organs by some of the investigated alloys should be considered if dental usage of these alloys is to be extended.

  4. Chemical-milling solution for invar alloy

    NASA Technical Reports Server (NTRS)

    Batiuk, W.

    1980-01-01

    Excellent surface finishes and tolerances are achieved using two formulations. Solution A gives finish of 3.17 micrometers after milling at 57 to 63 deg C. Constituents of A are: Hydrofluoric acid (70%), 5,8 oz/gal; nitric acid (40-42) degrees Baume), 40 oz/gal. Alternative solution gives 2.16 micrometer finish, and differs from A by addition of 7% phosphoric acid. Formulations eliminate channeling at root fillets, dishing, island formation, and overhangs.

  5. Improved Arterial Blood Oxygenation Following Intravenous Infusion of Cold Supersaturated Dissolved Oxygen Solution

    PubMed Central

    Grady, Daniel J; Gentile, Michael A; Riggs, John H; Cheifetz, Ira M

    2014-01-01

    BACKGROUND One of the primary goals of critical care medicine is to support adequate gas exchange without iatrogenic sequelae. An emerging method of delivering supplemental oxygen is intravenously rather than via the traditional inhalation route. The objective of this study was to evaluate the gas-exchange effects of infusing cold intravenous (IV) fluids containing very high partial pressures of dissolved oxygen (>760 mm Hg) in a porcine model. METHODS Juvenile swines were anesthetized and mechanically ventilated. Each animal received an infusion of cold (13 °C) Ringer’s lactate solution (30 mL/kg/hour), which had been supersaturated with dissolved oxygen gas (39.7 mg/L dissolved oxygen, 992 mm Hg, 30.5 mL/L). Arterial blood gases and physiologic measurements were repeated at 15-minute intervals during a 60-minute IV infusion of the supersaturated dissolved oxygen solution. Each animal served as its own control. RESULTS Five swines (12.9 ± 0.9 kg) were studied. Following the 60-minute infusion, there were significant increases in PaO2 and SaO2 (P < 0.05) and a significant decrease in PaCO2 (P < 0.05), with a corresponding normalization in arterial blood pH. Additionally, there was a significant decrease in core body temperature (P < 0.05) when compared to the baseline preinfusion state. CONCLUSIONS A cold, supersaturated dissolved oxygen solution may be intravenously administered to improve arterial blood oxygenation and ventilation parameters and induce a mild therapeutic hypothermia in a porcine model. PMID:25249764

  6. Improved arterial blood oxygenation following intravenous infusion of cold supersaturated dissolved oxygen solution.

    PubMed

    Grady, Daniel J; Gentile, Michael A; Riggs, John H; Cheifetz, Ira M

    2014-01-01

    One of the primary goals of critical care medicine is to support adequate gas exchange without iatrogenic sequelae. An emerging method of delivering supplemental oxygen is intravenously rather than via the traditional inhalation route. The objective of this study was to evaluate the gas-exchange effects of infusing cold intravenous (IV) fluids containing very high partial pressures of dissolved oxygen (>760 mm Hg) in a porcine model. Juvenile swines were anesthetized and mechanically ventilated. Each animal received an infusion of cold (13 °C) Ringer's lactate solution (30 mL/kg/hour), which had been supersaturated with dissolved oxygen gas (39.7 mg/L dissolved oxygen, 992 mm Hg, 30.5 mL/L). Arterial blood gases and physiologic measurements were repeated at 15-minute intervals during a 60-minute IV infusion of the supersaturated dissolved oxygen solution. Each animal served as its own control. Five swines (12.9 ± 0.9 kg) were studied. Following the 60-minute infusion, there were significant increases in PaO2 and SaO2 (P < 0.05) and a significant decrease in PaCO2 (P < 0.05), with a corresponding normalization in arterial blood pH. Additionally, there was a significant decrease in core body temperature (P < 0.05) when compared to the baseline preinfusion state. A cold, supersaturated dissolved oxygen solution may be intravenously administered to improve arterial blood oxygenation and ventilation parameters and induce a mild therapeutic hypothermia in a porcine model.

  7. Magnetic properties of Co-Cu metastable solid solution alloys

    NASA Astrophysics Data System (ADS)

    Fan, Xu; Mashimo, Tsutomu; Huang, Xinsheng; Kagayama, Tomoko; Chiba, Akira; Koyama, Keiichi; Motokawa, Mitsuhiro

    2004-03-01

    Metastable solid solution alloy powders and bulk alloys in the cobalt(Co)-copper(Cu) (10 90 mol % Co) system, which is an almost immiscible system at the ambient state, were prepared by mechanical alloying (MA) and shock compression. All MA-treated powders showed the x-ray diffraction patterns of a single phase of fcc structure. The lattice parameter increases with Cu concentration and is fundamentally on the line with Vegard’s law. The magnetization curves of CoxCu100-x (x=20 80) metastable bulk alloys at room temperature showed ferromagnetism, while the one of Co10Cu90 system showed paramagnetism. The saturation magnetic moment (Ms) curve versus electron numbers per atom at 0 K was found to be similar to the Slater-Pauling curves of other transition-metal binary systems and decreased with increasing Cu concentration and approached zero at about 28.8 electrons per atom. The magnetoresistance ratio at room temperature increased with Cu content in the ferromagnetic region, while the one of the paramagnetic Co10Cu90 alloy was negligibly small.

  8. Electrochemical Properties of Al-Cu Alloys in Nacl Solutions

    NASA Astrophysics Data System (ADS)

    Roman, Alejandra Silvina; Méndez, Claudia Marcela; Schvezov, Carlos Enrique; Ares, Alicia Esther

    In this paper the structure of aluminum based alloys and their corrosion behavior by using different electrochemical techniques as characterization methods are considered. Currently, it becomes imperative to know the role of the Al2Cu against the susceptibility to corrosion of these alloys. The present work aims to studying the electrochemical behavior of aluminum base alloys with the following compositions: Al-1wt.%Cu, Al-4.5wt.%Cu and Al-15wt.%Cu (with different grain structures), in 1M NaCl solutions, at room temperature. Cyclic potentiodynamic polarization tests were performed and were found that the alloys with more than 1wt.%Cu in the matrix have an unstable behavior and without tendency to reach passivity. The equivalent circuits derived from electrochemical impedance spectroscopy technique (EIS) generally showed two capacitive contributions. The susceptibility to corrosion becomes a complex function, not only of copper concentration and structure, but also with interdendritic spacings and distribution of phases in the alloys.

  9. Analysis of RFSA Campaign No.2 Dissolver Solution for Hg(I) and Hg(II)

    SciTech Connect

    Holcomb, H.P.

    2001-05-17

    TA 2-1083, under which RFSA processing is conducted, calls for a nominal mercuric ion concentration in the dissolver solution of 0.006M with a maximum of 0.01 M. The second RFSA campaign operated according to these guidelines with the initial Hg(II) concentration being 0.0068 M. Part of this study is to ascertain optimum excess Hg(I) for chloride removal.

  10. NMR discrimination in nonrigid prochiral solutes dissolved in chiral liquid crystals: symmetry considerations.

    PubMed

    Lesot, Philippe; Luz, Zeev; Aroulanda, Christie; Zimmermann, Herbert

    2014-10-01

    Enantiodiscrimination in the NMR spectra of flexible prochiral solutes dissolved in chiral liquid crystals (CLCs) is reviewed and compared with the analog phenomenon in such rigid solutes. In rigid prochiral solutes, the discrimination is brought about by the cancellation of improper symmetry elements upon dissolving in CLC within the frame of solute-solvent ordering mechanisms. If this reduction in symmetry renders the ordering of enantiotopic sites dissimilar, spectral discrimination may be observed. Symmetry considerations indicate that this is only possible for improper nonaxial groups lacking inversion symmetry. Nonrigid prochiral solutes consist of rapidly (on the NMR timescale) interconverting enantiomers, in which the racemization is accompanied by exchange of nonequivalent sites. These sites become, on the average, enantiotopically related, and in CLC, they exhibit spectral discrimination. The mechanism of the effect and the symmetry selection rules are different for the two cases. Specifically, the discrimination in flexible prochiral compounds results from the different ordering of the interchanging enantiomers in CLC. Using Altman's definition of average symmetry (Proc. R. Soc. A, 1967, 298, 184), selection rules for the phenomenon are derived. It follows that chiral discrimination in nonrigid prochiral solutes is much more abundant and can occur in all symmetry types except those possessing inversion. In particular, contrary to earlier thoughts, the effect can occur in compounds with axial symmetry. Illustrative examples of such studies with particular emphasis on compounds with average axial symmetry of the type D(3h), C(3v) and C(3h) are reviewed in this contribution.

  11. Electronic origin of solid solution softening in bcc molybdenum alloys.

    PubMed

    Medvedeva, N I; Gornostyrev, Yu N; Freeman, A J

    2005-04-08

    The intrinsic mechanism of solid solution softening in bcc molybdenum alloys due to 5d transition metal additions is investigated on the basis of ab initio electronic-structure calculations that model the effect of alloying elements on the generalized stacking fault (GSF) energies. We demonstrate that additions with an excess of electrons (Re, Os, Ir, and Pt) lead to a decrease in the GSF energy and those with a lack of electrons (Hf and Ta) to its sharp increase. Using the generalized Peierls-Nabarro model for a nonplanar core, we associate the local reduction of the GSF energy with an enhancement of double kink nucleation and an increase of the dislocation mobility, and we reveal the electronic reasons for the observed dependence of the solution softening on the atomic number of the addition.

  12. Quantitative prediction of solute strengthening in aluminium alloys

    NASA Astrophysics Data System (ADS)

    Leyson, Gerard Paul M.; Curtin, William A.; Hector, Louis G.; Woodward, Christopher F.

    2010-09-01

    Despite significant advances in computational materials science, a quantitative, parameter-free prediction of the mechanical properties of alloys has been difficult to achieve from first principles. Here, we present a new analytic theory that, with input from first-principles calculations, is able to predict the strengthening of aluminium by substitutional solute atoms. Solute-dislocation interaction energies in and around the dislocation core are first calculated using density functional theory and a flexible-boundary-condition method. An analytic model for the strength, or stress to move a dislocation, owing to the random field of solutes, is then presented. The theory, which has no adjustable parameters and is extendable to other metallic alloys, predicts both the energy barriers to dislocation motion and the zero-temperature flow stress, allowing for predictions of finite-temperature flow stresses. Quantitative comparisons with experimental flow stresses at temperature T=78K are made for Al-X alloys (X=Mg, Si, Cu, Cr) and good agreement is obtained.

  13. Effect of temperature and dissolved hydrogen on oxide films formed on Ni and Alloy 182 in simulated PWR water

    NASA Astrophysics Data System (ADS)

    Mendonça, R.; Bosch, R.-W.; Van Renterghem, W.; Vankeerberghen, M.; de Araújo Figueiredo, C.

    2016-08-01

    Alloy 182 is a nickel-based weld metal, which is susceptible to stress corrosion cracking in PWR primary water. It shows a peak in SCC susceptibility at a certain temperature and hydrogen concentration. This peak is related to the electrochemical condition where the Ni to NiO transition takes place. One hypothesis is that the oxide layer at this condition is not properly developed and so the material is not optimally protected against SCC. Therefore the oxide layer formed on Alloy 182 is investigated as a function of the dissolved hydrogen concentration and temperature around this Ni/NiO transition. Exposure tests were performed with Alloy 182 and Ni coupons in a PWR environment at temperatures between 300 °C and 345 °C and dissolved hydrogen concentration between 5 and 35 cc (STP)H2/kg. Post-test analysis of the formed oxide layers were carried out by SEM, EDS and XPS. The exposure tests with Ni coupons showed that the Ni/NiO transition curve is at a higher temperature than the curve based on thermodynamic calculations. The exposure tests with Alloy 182 showed that oxide layers were present at all temperatures, but that the morphology changed from spinel crystals to needle like oxides when the Ni/NiO transition curve was approached. Oxide layers were present below the Ni/NiO transition curve i.e. when the Ni coupon was still free of oxides. In addition an evolved slip dissolution model was proposed that could explain the observed experimental results and the peak in SCC susceptibility for Ni-based alloys around the Ni/NiO transition.

  14. Analytical and Numerical Solution for a Solidifying Liquid Alloy Slab

    NASA Technical Reports Server (NTRS)

    Antar, B. N.

    1983-01-01

    Numerical and analytical solutions are presented for the temperature and concentration distributions during the solidification of a binary liquid alloy slab. The slab is taken to be of a finite depth but infinite in the horizontal direction. The solidification process is started by withdrawing a fixed amount of heat from the lower surface of the slab. The upper surface of the slab is subjected to both radiation and convective conditions. The solution gives the concentration and temperature profiles and the interface position as a function of time. Due to the smallness of the mass diffusion coefficient in the solid, the numerical solution method breaks down whenever the ratio of the diffusivities in the solid and the liquid falls below a certain value. An analytical method is developed which gives accurate solution for any value of the diffusivity ratio.

  15. Effects of Dissolving Solutions on the Accuracy of an Electronic Apex Locator-Integrated Endodontic Handpiece

    PubMed Central

    Ustun, Yakup; Uzun, Ozgur; Er, Ozgur; Maden, Murat; Yalpı, Fatma; Canakci, Burhan Can

    2013-01-01

    The effects of three dissolving agents on the accuracy of an electronic apex locator- (EAL-) integrated endodontic handpiece during retreatment procedures were evaluated. The true lengths (TLs) of 56 extracted incisor teeth were determined visually. Twenty teeth were filled with gutta-percha and a resin-based sealer (group A), 20 with gutta-percha and a zinc oxide/eugenol-based sealer (group B), and 16 roots were used as the control group (group C). All roots were prepared to TL. Guttasolv, Resosolv, and Endosolv E were used as the dissolving solutions. Two evaluations of the handpiece were performed: the apical accuracy during the auto reverse function (ARL) and the apex locator function (EL) alone. The ARL function of the handpiece gave acceptable results. There were significant differences between the EL mode measurements and the TL (P < 0.05). In these comparisons, Tri Auto ZX EL mode measurements were significantly shorter than those of the TL. PMID:24379743

  16. Long-term corrosion investigation of AISI 316L, Co-28Cr-6Mo, and Ti-6Al-4V alloys in simulated body solutions

    NASA Astrophysics Data System (ADS)

    Karimi, Shima; Nickchi, Tirdad; Alfantazi, Akram M.

    2012-06-01

    The long-term weight loss, ion release and surface composition of AISI 316L, the Co-28Cr-6Mo and Ti-6Al-4V alloys were investigated in phosphate buffered solutions (PBS) with various bovine serum albumin (BSA) concentrations. All the samples lost weight up to 14 weeks and then started to gain weight. This can be explained by precipitation of dissolved ions on the surface after 14 weeks of immersion. The quantities of the dissolved ions were measured in immersed solution for 8, 14 and 22 weeks by induced coupled plasma-optical emission spectrometer (ICP-OES). The amounts of Fe released from 316L, and Co and Mo released from the Co-28Cr-6Mo alloy decreased after 14 weeks of immersion in PBS and BSA solutions. This observation coincides with the weight change of the samples. The oxide layer composition and concentration of the specimens exposed to solutions for 22 weeks were identified by X-ray photoelectron spectroscopy (XPS) analysis. The XPS results revealed that chromium is the main component of the 316L and Co-28Cr-6Mo alloy. The high Cr concentration of the 316L and Co-Cr-Mo oxide layer corresponds with the slow dissolution rate of Cr compared to other alloying elements of the 316L and Co-28Cr-6Mo alloy.

  17. Measurement of CO(2) Dissolved in Aqueous Solutions Using a Modified Infrared Gas Analyzer System.

    PubMed

    Schumacher, T E; Smucker, A J

    1983-05-01

    Total dissolved inorganic carbon (SigmaCO(2)) and aqueous carbon dioxide (H(2)CO(3) (*)) in nutrient solutions may be measured by the injection of small gas or liquid samples (1 microliter to 8 milliliters) into a gas stripping column connected in-line with an infrared gas analyzer. The measurement of SigmaCO(2) in solution requires sample acidification, while H(2)CO(3) (*) and gaseous CO(2) are measured without the addition of lactic acid. The standard curve for SigmaCO(2) was linear up to 300 nanomoles CO(2). Maximum sensitivity was approximately 300 picomoles. Measurements of H(2)CO(3) (*) were independent of pH. Consequently, SigmaCO(2) and H(2)CO(3) (*) could be used to calculate the pH, HCO(3) (-), and CO(3) (2-) values of nutrient solutions. Injection and complete analyses required from 0.8 to 2 minutes.

  18. Rheological behaviors and miscibility of mixture solution of polyaniline and cellulose dissolved in an aqueous system.

    PubMed

    Shi, Xingwei; Lu, Ang; Cai, Jie; Zhang, Lina; Zhang, Hongming; Li, Ji; Wang, Xianhong

    2012-08-13

    In our previous work, supramolecular films composed of hydrophilic cellulose and hydrophobic polyaniline (PANI) dissolved in NaOH/urea aqueous solution at low temperature through rearrangement of hydrogen bonds have been constructed. To further understand the miscibility and processability of the complex solution, the dynamic rheological behaviors of the PANI/cellulose complex solution were investigated, for the first time, in the present work. Transmission electron microscope (TEM) results demonstrated that the inclusion complexes consisted of PANI and cellulose, existed in the aqueous solution, showing a good miscibility. Time-temperatures superposition (tTs) results indicated that the PANI/cellulose solution exhibited a homogeneous system, and the complex solution was more stable than the cellulose solution in the temperature range from 5 to 25 °C. Winter-Chambon theory was proved to be capable of describing the gelation behavior of the PANI/cellulose complex solution. The relaxation exponent at the gel point was calculated to be 0.74, lower than the cellulose solution, indicating strong interactions between PANI and cellulose chains. Relatively larger flow activation energy of the PANI/cellulose solution suggested the formation and rupture of linkages in "junction zones" during the gelation processes. Furthermore, PANI/cellulose gels could form at elevated temperature as a result of the physical cross-linking and chain entanglement, and it was a thermoirreversible process. Moreover, the PANI/cellulose solution remained a liquid state for a long time at the temperature range from 0 to 8 °C, which is important for the industry process.

  19. Methods of deoxygenating metals having oxygen dissolved therein in a solid solution

    DOEpatents

    Zhang, Ying; Fang, Zhigang Zak; Sun, Pei; Xia, Yang; Zhou, Chengshang

    2017-06-06

    A method of deoxygenating metal can include forming a mixture of: a metal having oxygen dissolved therein in a solid solution, at least one of metallic magnesium and magnesium hydride, and a magnesium-containing salt. The mixture can be heated at a deoxygenation temperature for a period of time under a hydrogen-containing atmosphere to form a deoxygenated metal. The deoxygenated metal can then be cooled. The deoxygenated metal can optionally be subjected to leaching to remove by-products, followed by washing and drying to produce a final deoxygenated metal.

  20. Quaternary Ti-20Nb-10Zr-5Ta alloy during immersion in simulated physiological solutions: formation of layers, dissolution and biocompatibility.

    PubMed

    Milošev, Ingrid; Hmeljak, Julija; Žerjav, Gregor; Cör, Andrej; Calderon Moreno, Jose Maria; Popa, Monica

    2014-04-01

    Samples of the quaternary Ti-20Nb-10Zr-5Ta alloy were immersed in Hanks' simulated physiological solution and in minimum essential medium (MEM) for 25 days. Samples of Ti metal served as controls. During immersion, the concentration of ions dissolved in MEM was measured by inductively coupled plasma mass spectrometry, while at the end of the experiment the composition of the surface layers was analyzed by X-ray photoelectron spectroscopy, and their morphology by scanning electron microscopy equipped for chemical analysis. The surface layer formed during immersion was comprised primarily of TiO2 but contained oxides of alloying elements as well. The degree of oxidation differed for different metal cations; while titanium achieved the highest valency, tantalum remained as the metal or is oxidized to its sub-oxides. Calcium phosphate was formed in both solutions, while formation of organic-related species was observed only in MEM. Dissolution of titanium ions was similar for metal and alloy. Among alloying elements, zirconium dissolved in the largest quantity. The long-term effects of alloy implanted in the recipient's body were investigated in MEM, using two types of human cells-an osteoblast-like cell line and immortalized pulmonary fibroblasts. The in vitro biocompatibility of the quaternary alloy was similar to that of titanium, since no detrimental effects on cell survival, induction of apoptosis, delay of growth, or change in alkaline phosphatase activity were observed on incubation in MEM.

  1. In vitro corrosion of dental Au-based casting alloys in polyvinylpyrrolidone-iodine solution.

    PubMed

    Takasusuki, Norio; Ida, Yusuke; Hirose, Yukito; Ochi, Morio; Endo, Kazuhiko

    2013-01-01

    The corrosion and tarnish behaviors of two Au-based casting alloys (ISO type 1 and type 4 Au alloys) and their constituent pure metals, Au, Ag, Cu, Pt, and Pd in a polyvinylpyrrolidone-iodine solution were examined. The two Au alloys actively corroded, and the main anodic reaction for both was dissolution of Au as AuI₂(-). The amount of Au released from the ISO type 1 Au alloy was significantly larger than that from the ISO type 4 Au alloy (P<0.05). Visible light spectrophotometry revealed that the type 1 alloy exhibited higher susceptibility to tarnishing than the type 4 alloy. The corrosion forms of the two Au alloys were found to be completely different, i.e., the type 1 alloy exhibited the corrosion attack over the entire exposed surface with a little irregularity whereas the type 4 alloy exhibited typical intergranular corrosion, which was caused by local cells produced by segregation of Pd and Pt.

  2. Rock Physics Characterization of Porous Media Containing Hydrates Formed Out of Solution: Tetrathydrofuran VS. Dissolved Methane

    NASA Astrophysics Data System (ADS)

    Schicks, J. M.; Rydzy, M. B.; Spangenberg, E.; Batzle, M. L.

    2012-12-01

    Methane hydrate formation in sediments from the dissolved gas phase is a tedious and time-consuming task, due to the relatively low solubility of methane in water. A number of studies on physical properties of hydrated sediments have been conducted on sediments containing tetrahydrofuran (THF) hydrates instead. The use of THF as a hydrate former is convenient as it forms hydrate at atmospheric pressure and relatively high temperatures of about 277 K. It is completely miscible in water, thus forms hydrate out solution and promises homogeneous synthesis of THF hydrate in sediment. The applicability of THF as a proxy for methane hydrate formed out of solution, however, has often been questioned. To better understand whether THF hydrates represent a legitimate proxy for methane hydrates formed out of solution, ultrasonic velocity and resistivity measurements were performed on hydrated Ottawa Sand F110 sand and glass bead samples in conjunction with imaging techniques, such as micro X-ray computed tomography (MXCT), and scanning electron microscopy (SEM). Thereby the tests were conducted on samples containing hydrates formed both, from methane dissolved in water and with the use of THF. The results show, that in terms of ultrasonic velocities, THF and methane hydrates exhibit the same trend. As the hydrate crystallized in the pore space, no increase in velocity was observed until a critical hydrate saturation of 35-50 percent was exceeded. On the other hand, the bulk electrical resistivity increased with increasing gas hydrate saturation. Comparison with current rock physics models suggested that the gas hydrate formed out of solution in both cases exhibits pore-filling/ load-bearing behavior, i.e. it suggests that the hydrate is formed away from the grains. This was supported through the imaging. This series of measurements provided the first direct comparison of THF and methane hydrates formed out of solution in terms of how their distribution and location in the pore

  3. Corrosion Behavior of Alloy 22 in Chloride Solutions Containing Organic Acids

    SciTech Connect

    Carranza, R M; Giordano, C M; Rodr?guez, M A; Rebak, R B

    2005-11-04

    Alloy 22 (N06022) is a nickel based alloy containing alloying elements such as chromium, molybdenum and tungsten. It is highly corrosion resistant both under reducing and under oxidizing conditions. Electrochemical studies such as electrochemical impedance spectroscopy (EIS) were performed to determine the corrosion behavior of Alloy 22 in 1M NaCl solutions at various pH values from acidic to neutral at 90 C. Tests were also carried out in NaCl solutions containing oxalic acid or acetic acid. It is shown that the corrosion rate of Alloy 22 was higher in a solution containing oxalic acid than in a solution of the same pH acidified with HCl. Acetic acid was not corrosive to Alloy 22. The corrosivity of oxalic acid was attributed to its capacity to form stable complex species with metallic cations from Alloy 22.

  4. Urothelial injury to the rabbit bladder caused by calcium dissolving agents including two new citrate solutions.

    PubMed

    Zhang, Xiang-bo; Wang, Zhi-ping; Duan, Jian-min; Duan, Guo-lan; Shi, Ting-kai; Lu, Jian-zhong; Ma, Bao-liang

    2005-08-01

    We compared the urothelial injury to the bladder caused by four agents capable of dissolving calcium salts. The solutions were administrated in an antegrade way through left ureterostomies in 54 rabbits for periods of 24, 48 and 72 h. The bladders were then removed and three routine histological sections were made for each. The following six solutions were used: physiological sodium chloride solution (Phys), artificial urine (Art), 0.03 M disodium EDTA buffered to pH 8.5 with triethanolamine (EDTA), 10% Renacidin (R), test solution 2 (S2, using D-gluconic acid-lactone and other compounds that differ from R in terms of ingredients or quantity), and test solution 1 (S1, using D-gluconic-acid instead of D-gluconic acid-lactone in S2 but keeping the other ingredients the same) for irrigation. At 24 h there was no observable urothelial damage caused by perfusion with Phys or Art; solutions R, S1 and S2 caused approximately the same level of injury to the rabbit bladder mucosa; however, irrigation with disodium-EDTA caused more serious urothelial injury than R, S1 and S2 (P<0.05, chi2-test) and may be unacceptable. The damage to bladder tissues treated with S1 and S2 was less than that caused by R, but this was not significant (P>0.05, chi2-test). Following a prolonged irrigation time, all of these solutions cause further urothelial damage, but EDTA caused the most, followed by R, S1, S2, Phys or Art, respectively, at 48 and 72 h. In view of the better solubility effect of solutions S1 and S2 compared with R, it might be justified in accepting the more pronounced urothelial irritation caused these solutions, but in order to enhance their effectiveness and reduce urothelial injury further study will be needed.

  5. Simultaneous measurements of plutonium and uranium in spent-fuel dissolver solutions

    SciTech Connect

    Li, T.K.; Kuno, T.; Kitagawa, O.; Sato, S.; Kurosawa, A.; Kuno, Y.

    1997-11-01

    The authors have studied the isotope dilution gamma-ray spectrometry (IDGS) technique for simultaneous measurements of elemental concentrations and isotopic compositions for both plutonium and uranium in input spent-fuel dissolver solutions at a reprocessing plant. The technique under development includes both sample preparation and analysis methods. For simultaneous measurements of both plutonium and uranium, a critical issue is to develop a new method to keep both plutonium and uranium in the sample after they are separated from fission products. Furthermore, it is equally important to improve the analysis method so that the precision and accuracy of the plutonium analysis remain unaffected while uranium is retained in the sample. To keep both plutonium and uranium in the sample for simultaneous measurements, extraction chromatography is being studied and shows promise to achieve the goal of cosegregation of the plutonium and uranium. The technique uses U/TEVA{center_dot}Spec resin to separate fission products and recover both uranium and plutonium in the resin from dissolver solutions for subsequent measuring using high-resolution gamma-ray spectrometry. Owing to the fact that the U/Pu ratio is altered during the fission product separation phase, it is necessary to develop a method which could accurately correct for this effect. Such a method was developed using the unique decay properties of {sup 241}Pu to {sup 237}U and shows considerable promise in allowing for accurate determination of the {sup 235}U concentrations before the chemical extraction.

  6. [Dynamic change of dissolved iron in wetland soil solutions responding to freeze-thaw cycles].

    PubMed

    Yu, Xiao-fei; Wang, Guo-ping; Lü, Xian-guo; Zou, Yuan-chun; Jiang, Ming

    2010-05-01

    The effects of five freeze-thaw cycles on the dynamic change of dissolved iron in three typical wetland soils (humus marsh soil in Carex lasiocarpa community, meadow marsh soil in Cares meyeriarna community, and meadow albic soil in Calamagrostis angustifolia community)of Sanjiang Plain, Northeast China, was analyzed through in-situ soil column simulation. One freeze-thaw cycle was conducted as freezing at -10 degrees C for 1 d and then thawing at 5 degrees C for 7 d. The thermostatically incubated soils at 5 degrees C were controls. The results showed that most pH and Eh values increased after the first freeze-thaw cycle, and then decreased after the subsequent cycles. 84.4% of the pH values of freeze-thaw treated soils were smaller than that of control, while 82.2% of the Eh values of freeze-thaw treated soils were greater than that of control. Most of the dissolved iron in all soil solutions were Fe3+ ions and colloids, and the reduction of these Fe3+ species were inhibited. The concentrations of Fe2, Fe3+, and total dissolved iron (TFe) of the freeze-thaw treated soils were all smaller than that of controls, with the means of (0.62 +/- 0.08) mg x L(-1) and (1.25 +/- 0.16) mg x L(-1), respectively. The variation trends of pH, Eh, and dissolved iron in the humus marsh soil were significantly different from that in the meadow albic soil. The trends in the meadow marsh soil, as the transitional soil type, were more similar to the meadow albic soil for pH, while more similar to the humus marsh soil for Eh and dissolved iron. Among the three soils, the difference between freeze-thaw treated columns and controls of the second layer were all smaller than that of the third and fourth layer, which indicated that the effect of freeze-thaw cycles were more significant for the upper annular wetland soil layers than the lower layers.

  7. Metal Ion Speciation and Dissolved Organic Matter Composition in Soil Solutions

    NASA Astrophysics Data System (ADS)

    Benedetti, M. F.; Ren, Z. L.; Bravin, M.; Tella, M.; Dai, J.

    2014-12-01

    Knowledge of the speciation of heavy metals and the role of dissolved organic matter (DOM) in soil solution is a key to understand metal mobility and ecotoxicity. In this study, soil column-Donnan membrane technique (SC-DMT) was used to measure metal speciation of Cd, Cu, Ni, Pb, and Zn in eighteen soil solutions, covering a wide range of metal sources and concentrations. DOM composition in these soil solutions was also determined. Our results show that in soil solution Pb and Cu are dominant in complex form, whereas Cd, Ni and Zn mainly exist as free ions; for the whole range of soil solutions, only 26.2% of DOM is reactive and consists mainly of fulvic acid (FA). The metal speciation measured by SC-DMT was compared to the predicted ones obtained via the NICA-Donnan model using the measured FA concentrations. The free ion concentrations predicted by speciation modelling were in good agreement with the measurements. Diffusive gradients in thin-films gels (DGT) were also performed to quantify the labile metal species in the fluxes from solid phase to solution in fourteen soils. The concentrations of metal species detected by DGT were compared with the free ion concentrations measured by DMT and the maximum concentrations calculated based on the predicted metal speciation in SC-DMT soil solutions. It is concluded that both inorganic species and a fraction of FA bound species account for the amount of labile metals measured by DGT, consistent with the dynamic features of this technique. The comparisons between measurements using analytical techniques and mechanistic model predictions provided mutual validation in their performance. Moreover, we show that to make accurate modelling of metal speciation in soil solutions, the knowledge of DOM composition is the crucial information, especially for Cu; like in previous studies the modelling of Pb speciation is not optimal and an updated of Pb generic binding parameters is required to reduce model prediction uncertainties.

  8. Dissolved organic carbon in soil solution of peat-moorsh soils on Kuwasy Mire

    NASA Astrophysics Data System (ADS)

    Jaszczyński, J.; Sapek, A.

    2009-04-01

    Key words: peat-moorsh soils, soil solution, dissolved organic carbon (DOC), temperature of soil, redox potential. The objective this study was the dissolved organic carbon concentration (DOC) in soil solution on the background of soil temperature, moisture and redox potential. The investigations were localized on the area of drained and agricultural used Kuwasy Mire, which are situated in the middle basin of Biebrza River, in North-East Poland. Research point was placed on a low peat soil of 110 cm depth managed as extensive grassland. The soil was recognized as peat-moorsh with the second degree of the moorshing process (with 20 cm of moorsh layer). The ceramic suction cups were installed in three replications at 30 cm depth of soil profile. The soil solution was continuously sampled by pomp of the automatic field station. The successive samples comprised of solution collected at the intervals of 21 days. Simultaneously, at the 20, 30 and 40 cm soil depths the measurements of temperature and determination of soil moisture and redox potential were made automatically. The mean twenty-four hours data were collected. The concentrations of DOC were determined by means of the flow colorimeter using the Skalar standard methods. Presented observations were made in 2001-2006. Mean DOC concentration in soil solution was 66 mg.dm-3 within all research period. A significant positive correlation between studied compound concentration and temperature of soil at 30 cm depth was observed; (correlation coefficient - r=0.55, number of samples - n=87). The highest DOC concentrations were observed during the season from July to October, when also a lower ground water level occurred. The DOC concentration in soil solution showed as well a significant correlation with the soil redox potential at 20 cm level. On this depth of describing soil profile a frontier layer between moorshing layer and peat has been existed. This layer is the potentially most active in the respect to

  9. The Effect of Solution Annealing on Alloy 22 Weld Properties

    SciTech Connect

    El-Dasher, B S; Torres, S G

    2005-11-08

    The effect of solution annealing temperature on the microstructure and observed corrosion attack mode in Alloy 22 welds was assessed. Specimens were examined in the as-welded state as well as solution annealed for 20 minutes at temperatures ranging from 1075 C to 1300 C. The microstructures of the specimens were first mapped using electron backscatter diffraction to determine the grain structure evolution due to solution annealing. Full recrystallization of the fusion zone was only observed in the 1200 C and 1300 C specimens, although the 1300 C specimen showed abnormal grain growth. As-welded, 1121 C and 1200 C specimens were also subjected to electrochemical testing in a 6 molal NaCl + 0.9 molal KNO{sub 3} environment to initiate crevice corrosion. Examination of the specimen surfaces after corrosion testing showed that in the as-welded specimen, corrosion was present in both the weld dendrites as well as around the secondary phases. However, the specimen solution annealed at 1121 C showed corrosion only at secondary phases and the specimen annealed at 1200 C showed pitting corrosion only in a handful of grains.

  10. Dissolving cellulose with twin-screw extruder in a NaOH complex aqueous solution

    NASA Astrophysics Data System (ADS)

    Yang, Y. P.; Zhang, Y.; Dawelbeit, A.; Yu, M. H.

    2016-07-01

    Novel cellulose dissolution method with twin-screw extruder was developed in order to improve the dissolution property, to simplify production procedure and to produce cellulose spinning dope which is stable and which has a higher concentration of cellulose. Therefore, the extrusion conditions on the cellulose dissolution in NaOH/thiourea/urea were extensively studied in this work. The resulted extrudates of twin-screw extruder dissolution method were characterized by polarized optical microscope image, the solubility experiment and the apparent viscosity. The results revealed that the screw revolution speed of such process could improve the solubility value (S a) of cellulose, and the solubility of cellulose reached a maximum value of 7.5 wt% at higher revolutions 450 rpm. On the other hand, the cellulose solutions were more transparent and balanced with its apparent viscosity values lower and more stable compare to stirring method, which indicated dissolving cellulose with twin-screw extruder was reliable. Moreover, the whole dissolving time is quite short, and the process is simple. The soluble effect of twin screw extrusion was far superior to traditional stirring, and the most suitable temperature was -2°C.

  11. Effects of Chromophoric Dissolved Organic Matter on Anthracene Photolysis Kinetics in Aqueous Solution and Ice.

    PubMed

    Malley, Philip P A; Grossman, Jarod N; Kahan, Tara F

    2017-09-27

    We measured photolysis kinetics of the PAH anthracene in aqueous solution, in bulk ice, and at ice surfaces in the presence and absence of chromophoric dissolved organic matter (CDOM). Self-association, which occurs readily at ice surfaces, may be responsible for the faster anthracene photolysis observed there. Photolysis rate constants in liquid water increased under conditions where anthracene self-association was observed. Concomitantly, kinetics changed from first-order to second-order, indicating that the photolysis mechanism at ice surfaces might be different than that in aqueous solution. Other factors that could lead to faster photolysis at ice surfaces were also investigated. Increased photon fluxes due to scattering in the ice samples can account for at most 20% of the observed rate increase, and other factors including singlet oxygen ((1)O2*) production and changes in pH and polarity were determined not to be responsible for the faster photolysis. CDOM (in the form of fulvic acid (FA)) did not affect anthracene photolysis kinetics in aqueous solution but suppressed photolysis in ice cubes and ice granules (by 30% and 56%, respectively). This was primarily due to competitive photon absorption (the inner filter effect). Freeze-concentration (or "salting out") appears to slightly increase the suppressing effects of FA on anthracene photolysis. This may be due to increased competitive photon absorption or to physical interactions between anthracene and FA.

  12. Trends in soil solution dissolved organic carbon (DOC) concentrations across European forests

    NASA Astrophysics Data System (ADS)

    Camino-Serrano, Marta; Graf Pannatier, Elisabeth; Vicca, Sara; Luyssaert, Sebastiaan; Jonard, Mathieu; Ciais, Philippe; Guenet, Bertrand; Gielen, Bert; Peñuelas, Josep; Sardans, Jordi; Waldner, Peter; Etzold, Sophia; Cecchini, Guia; Clarke, Nicholas; Galić, Zoran; Gandois, Laure; Hansen, Karin; Johnson, Jim; Klinck, Uwe; Lachmanová, Zora; Lindroos, Antti-Jussi; Meesenburg, Henning; Nieminen, Tiina M.; Sanders, Tanja G. M.; Sawicka, Kasia; Seidling, Walter; Thimonier, Anne; Vanguelova, Elena; Verstraeten, Arne; Vesterdal, Lars; Janssens, Ivan A.

    2016-10-01

    Dissolved organic carbon (DOC) in surface waters is connected to DOC in soil solution through hydrological pathways. Therefore, it is expected that long-term dynamics of DOC in surface waters reflect DOC trends in soil solution. However, a multitude of site studies have failed so far to establish consistent trends in soil solution DOC, whereas increasing concentrations in European surface waters over the past decades appear to be the norm, possibly as a result of recovery from acidification. The objectives of this study were therefore to understand the long-term trends of soil solution DOC from a large number of European forests (ICP Forests Level II plots) and determine their main physico-chemical and biological controls. We applied trend analysis at two levels: (1) to the entire European dataset and (2) to the individual time series and related trends with plot characteristics, i.e., soil and vegetation properties, soil solution chemistry and atmospheric deposition loads. Analyses of the entire dataset showed an overall increasing trend in DOC concentrations in the organic layers, but, at individual plots and depths, there was no clear overall trend in soil solution DOC. The rate change in soil solution DOC ranged between -16.8 and +23 % yr-1 (median = +0.4 % yr-1) across Europe. The non-significant trends (40 %) outnumbered the increasing (35 %) and decreasing trends (25 %) across the 97 ICP Forests Level II sites. By means of multivariate statistics, we found increasing trends in DOC concentrations with increasing mean nitrate (NO3-) deposition and increasing trends in DOC concentrations with decreasing mean sulfate (SO42-) deposition, with the magnitude of these relationships depending on plot deposition history. While the attribution of increasing trends in DOC to the reduction of SO42- deposition could be confirmed in low to medium N deposition areas, in agreement with observations in surface waters, this was not the case in high N deposition areas. In

  13. In vitro corrosion of dental Ag-based alloys in polyvinylpyrrolidone iodine solution.

    PubMed

    Ochi, Morio; Endo, Kazuhiko; Ohno, Hiroki; Takasusuki, Norio; Matsubara, Hideki; Maida, Takeo

    2005-09-01

    The corrosion and tarnish behaviors of three Ag-based alloys (Ag-Pd-Cu-Au alloy, Ag-In alloy, and Ag-Sn-Zn alloy) in polyvinylpyrrolidone iodine (povidone-iodine) solution were examined. The degree of tarnish was evaluated by visible-ray spectrocolorimetry. Corrosion potential measurements and analyses of corrosion products by X-ray diffractometry were carried out to elucidate the corrosion mechanism. The corrosion rate of the three Ag-based alloys in povidone-iodine solution at its practical concentration used as a gargle solution was so fast that the alloys tarnished within 10 seconds of immersion with the formation of AgI. Thermodynamic consideration and the results of surface analysis by X-ray diffractometry revealed that the main anodic and cathodic reactions were Ag + I(-)-->AgI + e- and I2 + 2e(-)-->2I- respectively.

  14. Properties of low power spark ablation in aqueous solution for dissolution of precious metals and alloys

    NASA Astrophysics Data System (ADS)

    Goltz, Douglas; Boileau, Michael; Plews, Ian; Charleton, Kimberly; Hinds, Michael W.

    2006-07-01

    Spark ablation or electric dispersion of metal samples in aqueous solution can be a useful approach for sample preparation. The ablated metal forms a stable suspension that has been described as colloidal, which is easily dissolved with a small amount of concentrated (16 M) HNO 3. In this study, we have examined some of the properties of the spark ablation process for a variety of metals (Rh and Au) and alloys (stainless steel) using a low power spark (100-300 W). Particle size distributions and conductivity measurements were carried out on selected metals to characterize the stable suspensions. A LASER diffraction particle size analyzer was useful for showing that ablated particles varied in size from 1 to 30 μm for both the silver and the nickel alloy, Inconel. In terms of weight percent most of the particles were between 10 and 30 μm. Conductivity of the spark ablation solution was found to increase linearly for approximately 3 min before leveling off at approximately 300 S cm 3. These measurements suggest that a significant portion of the ablated metal is also ionic in nature. Scanning electron microscope measurements revealed that a low power spark is much less damaging to the metal surface than a high power spark. Crater formation of the low power spark was found in a wider area than expected with the highest concentration where the spark was directed. The feasibility of using spark ablation for metal dissolution of a valuable artifact such as gold was also performed. Determinations of Ag (4-12%) and Cu (1-3%) in Bullion Reference Material (BRM) gave results that were in very good agreement with the certified values. The precision was ± 0.27% for Ag at 4.15% (RSD = 6.5%) and ± 0.09% for Cu at 1% (RSD = 9.0%).

  15. Adsorption and desorption of dissolved organic matter by carbon nanotubes: Effects of solution chemistry.

    PubMed

    Engel, Maya; Chefetz, Benny

    2016-06-01

    Increasing use of carbon nanotubes (CNTs) has led to their introduction into the environment where they can interact with dissolved organic matter (DOM). This study focuses on solution chemistry effects on DOM adsorption/desorption processes by single-walled CNTs (SWCNTs). Our data show that DOM adsorption is controlled by the attachment of DOM molecules to the SWCNTs, and that the initial adsorption rate is dependent on solution parameters. Adsorbed amount of DOM at high ionic strength was limited, possibly due to alterations in SWCNT bundling. Desorption of DOM performed at low pH resulted in additional DOM adsorption, whereas at high pH, adsorbed DOM amount decreased. The extent of desorption conducted at increased ionic strength was dependent on pre-adsorbed DOM concentration: low DOM loading stimulated additional adsorption of DOM, whereas high DOM loading facilitated release of adsorbed DOM. Elevated ionic strength and increased adsorbed amount of DOM reduced the oxidation temperature of the SWCNTs, suggesting that changes in the assembly of the SWCNTs had occurred. Moreover, DOM-coated SWCNTs at increased ionic strength provided fewer sites for atrazine adsorption. This study enhances our understanding of DOM-SWCNT interactions in aqueous systems influenced by rapid changes in salinity, and facilitates potential use of SWCNTs in water-purification technologies.

  16. ELECTROCHEMICAL IMPEDANCE ANALYSIS OF beta-TITANIUM ALLOYS AS IMPLANTS IN RINGERS LACTATE SOLUTION

    SciTech Connect

    Bhola, Rahul; Bhola, Shaily M.; Mishra, Brajendra; Olson, David L.

    2010-02-22

    Commercially pure titanium and two beta-titanium alloys, TNZT and TMZF, have been characterized using various electrochemical techniques for their corrosion behavior in Ringers lactate solution. The variation of corrosion potential and solution pH with time has been discussed. Electrochemical Impedance Spectroscopy has been used to fit the results into a circuit model. The stability of the oxides formed on the surface of these alloys has been correlated with impedance phase angles. Cyclic Potentiodynamic Polarization has been used to compute the corrosion parameters for the alloys. TMZF is found to be a better beta-alloy as compared to TNZT.

  17. Comparative pharmacokinetic studies of fast dissolving film and oral solution of ondansetron in rats.

    PubMed

    Choudhary, Dhagla R; Patel, Vishnu A; Chhalotiya, Usmangani K; Patel, Harsha V; Kundawala, Aliasgar J

    2013-12-01

    Ondansetron, selective serotonin (5-HT3) receptor blocker, is used in treating chemotherapy induced nausea and vomiting in cancer patients. Mouth dissolving films containing ondansetron were developed to have better onset and patient compliances. The drug content of prepared films was within 85%-115%. The films were found to be stable for 4 months when stored at 40 %°C and 75% RH. In-vitro dissolution studies suggested a rapid disintegration, in which most of ondansetron was released (91.5±3.4%) within 90 sec. Subsequently, Sprague-Dawley rats were used to compare pharmacokinetic parameters of the formulated films with oral administration of pure drug solution. Pharmacokinetic parameters were similar between the two groups in which AUC0-t (ng h/ml), AUC0-∞ (ng h/ml), Cmax (ng/ml), Tmax (min), Kel (h(-1)) and t1/2 (h) of reference was 109.091±15.73, 130.32±18.56, 28.5±4.053, 60, 0.1860±0.0226, and 3.771±0.498 respectively; and for formulated film 113.663±16.64, 151.79±16.54, 30±3.51, 60, 0.1521±0.0310 and 4.755±0.653 respectively. These results suggest that the fast dissolving film containing ondansetron is likely to become one of the choices to treat chemotherapy induced nausea and vomiting.

  18. Local Structure and Short-Range Order in a NiCoCr Solid Solution Alloy

    DOE PAGES

    Zhang, F. X.; Zhao, Shijun; Jin, Ke; ...

    2017-05-19

    Multi-element solid solution alloys are intrinsically disordered on the atomic scale, and many of their advanced properties originate from the unique local structural characteristics. We measured the local structure of a NiCoCr solid solution alloy with X-ray/neutron total scattering and extended X-ray absorption fine structure (EXAFS) techniques. The atomic pair distribution function analysis (PDF) did not exhibit distinct structural distortion. But, EXAFS analysis suggested that the Cr atoms are favorably bonded with Ni and Co in the solid solution alloys. This short-range order (SRO) plays a role in the distinct low values of electrical and thermal conductivities in Ni-based solidmore » solution alloys when Cr is incorporated. Both the long-range and local structures of the NiCoCr alloy upon Ni ion irradiation were studied and an irradiation-induced enhancement of SRO was found.« less

  19. Local Structure and Short-Range Order in a NiCoCr Solid Solution Alloy

    NASA Astrophysics Data System (ADS)

    Zhang, F. X.; Zhao, Shijun; Jin, Ke; Xue, H.; Velisa, G.; Bei, H.; Huang, R.; Ko, J. Y. P.; Pagan, D. C.; Neuefeind, J. C.; Weber, W. J.; Zhang, Yanwen

    2017-05-01

    Multielement solid solution alloys are intrinsically disordered on the atomic scale, and many of their advanced properties originate from the local structural characteristics. The local structure of a NiCoCr solid solution alloy is measured with x-ray or neutron total scattering and extended x-ray absorption fine structure (EXAFS) techniques. The atomic pair distribution function analysis does not exhibit an observable structural distortion. However, an EXAFS analysis suggests that the Cr atoms are favorably bonded with Ni and Co in the solid solution alloys. This short-range order (SRO) may make an important contribution to the low values of the electrical and thermal conductivities of the Cr-alloyed solid solutions. In addition, an EXAFS analysis of Ni ion irradiated samples reveals that the degree of SRO in NiCoCr alloys is enhanced after irradiation.

  20. Electrolytic dissolver

    DOEpatents

    Wheelwright, E.J.; Fox, R.D.

    1975-08-26

    This patent related to an electrolytic dissolver wherein dissolution occurs by solution contact including a vessel of electrically insulative material, a fixed first electrode, a movable second electrode, means for insulating the electrodes from the material to be dissolved while permitting a free flow of electrolyte therebetween, means for passing a direct current between the electrodes and means for circulating electrolyte through the dissolver. (auth)

  1. High temperature and high pressure corrosion of nickel-based alloys and stainless steels in ammoniacal sulphate solution

    NASA Astrophysics Data System (ADS)

    Asselin, Edouard

    The corrosion characteristics of Alloy 625 (UNS 00625, Ni-22 Cr-10 Mo) in oxygenated ammoniacal sulphate environments are determined at room temperature and pressure and up to high temperatures and pressures (673 K, 250 bar) commensurate with the process of supercritical water oxidation (SCWO). Electrochemical methods such as linear polarization, potentiodynamic polarization and impedance spectroscopy are used. It is found that the electrochemical and morphological response is dictated by the alloying element Cr and the formation of a Cr(III) oxide. Mo and, to a lesser extent Ni, are found to dissolve readily. Thermodynamic analysis of the Ni-NH3-H2O system, including new Pourbaix diagrams at temperatures as high as 653 K, has shown that Ni-ammine formation is possible at moderate temperatures but that the stability of these complexes decreases substantially with temperature. According to one of the models investigated, which is based on the only available high temperature equilibrium constant data, Ni-ammines become unstable above approximately 473 K. Impedance spectroscopy has shown that transpassive dissolution of the alloy's p-type, cation conducting, Cr(III) oxide occurs at temperatures as low as 373 K and total pressure (oxygen saturated) as low as 40 bar. As temperature and pressure are increased the corrosion process is increasingly diffusion controlled. Transpassive dissolution results in the thinning and eventual total removal of the alloy's protective semiconductor barrier layer. Cation ejection from the barrier layer into the solution and porous outer layer phase results in precipitation of a Cr(III) scale (oxide or hydroxyl-oxide) at the alloy surface which acts as a diffusion barrier. It is hypothesized that the outer layer is either physically removed at supercritical conditions due to rapid dissolution and grain boundary attack of the alloy or chemically removed by solution acidification due to the formation of sulphuric acid at high density

  2. Accelerated exploration of multi-principal element alloys with solid solution phases

    NASA Astrophysics Data System (ADS)

    Senkov, O. N.; Miller, J. D.; Miracle, D. B.; Woodward, C.

    2015-03-01

    Recent multi-principal element, high entropy alloy (HEA) development strategies vastly expand the number of candidate alloy systems, but also pose a new challenge—how to rapidly screen thousands of candidate alloy systems for targeted properties. Here we develop a new approach to rapidly assess structural metals by combining calculated phase diagrams with simple rules based on the phases present, their transformation temperatures and useful microstructures. We evaluate over 130,000 alloy systems, identifying promising compositions for more time-intensive experimental studies. We find the surprising result that solid solution alloys become less likely as the number of alloy elements increases. This contradicts the major premise of HEAs—that increased configurational entropy increases the stability of disordered solid solution phases. As the number of elements increases, the configurational entropy rises slowly while the probability of at least one pair of elements favouring formation of intermetallic compounds increases more rapidly, explaining this apparent contradiction.

  3. Accelerated exploration of multi-principal element alloys with solid solution phases.

    PubMed

    Senkov, O N; Miller, J D; Miracle, D B; Woodward, C

    2015-03-05

    Recent multi-principal element, high entropy alloy (HEA) development strategies vastly expand the number of candidate alloy systems, but also pose a new challenge--how to rapidly screen thousands of candidate alloy systems for targeted properties. Here we develop a new approach to rapidly assess structural metals by combining calculated phase diagrams with simple rules based on the phases present, their transformation temperatures and useful microstructures. We evaluate over 130,000 alloy systems, identifying promising compositions for more time-intensive experimental studies. We find the surprising result that solid solution alloys become less likely as the number of alloy elements increases. This contradicts the major premise of HEAs--that increased configurational entropy increases the stability of disordered solid solution phases. As the number of elements increases, the configurational entropy rises slowly while the probability of at least one pair of elements favouring formation of intermetallic compounds increases more rapidly, explaining this apparent contradiction.

  4. Accelerated exploration of multi-principal element alloys with solid solution phases

    PubMed Central

    Senkov, O.N.; Miller, J.D.; Miracle, D.B.; Woodward, C.

    2015-01-01

    Recent multi-principal element, high entropy alloy (HEA) development strategies vastly expand the number of candidate alloy systems, but also pose a new challenge—how to rapidly screen thousands of candidate alloy systems for targeted properties. Here we develop a new approach to rapidly assess structural metals by combining calculated phase diagrams with simple rules based on the phases present, their transformation temperatures and useful microstructures. We evaluate over 130,000 alloy systems, identifying promising compositions for more time-intensive experimental studies. We find the surprising result that solid solution alloys become less likely as the number of alloy elements increases. This contradicts the major premise of HEAs—that increased configurational entropy increases the stability of disordered solid solution phases. As the number of elements increases, the configurational entropy rises slowly while the probability of at least one pair of elements favouring formation of intermetallic compounds increases more rapidly, explaining this apparent contradiction. PMID:25739749

  5. Corrosion behavior of pure titanium and titanium alloys in fluoride-containing solutions.

    PubMed

    Nakagawa, M; Matsuya, S; Udoh, K

    2001-12-01

    The effects of fluoride concentrations and pH on the corrosion behavior of pure titanium, Ti-6Al-4V, Ti-6Al-7Nb alloys and a new Ti alloy adding palladium, which is expected to promote a repassivation of Ti were examined by anodic polarization and corrosion potential measurements. The amount of dissolved Ti was analyzed by inductively coupled plasma mass spectroscopy. The surface of the specimen was analyzed by X-ray photoelectron spectroscopy before and after the measurement. Pure Ti, Ti-6Al-4V and Ti-6Al-7Nb alloys were easily corroded even in a low fluoride concentration in an acidic environment. The corrosion resistance of Ti-0.2Pd alloy was greater than those of pure Ti, Ti-6Al-4V and Ti-6Al-7Nb alloys in the wide range of pH and fluoride concentrations. The high corrosion resistance of Ti-0.2Pd alloy was caused by the surface enrichment of Pd promoting a repassivation of Ti. The Ti-0.2Pd alloy is expected to be useful as a new Ti alloy with high corrosion resistance in dental use.

  6. Photoproduction of hydrogen peroxide in aqueous solution from model compounds for chromophoric dissolved organic matter (CDOM).

    PubMed

    Clark, Catherine D; de Bruyn, Warren; Jones, Joshua G

    2014-02-15

    To explore whether quinone moieties are important in chromophoric dissolved organic matter (CDOM) photochemistry in natural waters, hydrogen peroxide (H2O2) production and associated optical property changes were measured in aqueous solutions irradiated with a Xenon lamp for CDOM model compounds (dihydroquinone, benzoquinone, anthraquinone, napthoquinone, ubiquinone, humic acid HA, fulvic acid FA). All compounds produced H2O2 with concentrations ranging from 15 to 500 μM. Production rates were higher for HA vs. FA (1.32 vs. 0.176 mM h(-1)); values ranged from 6.99 to 0.137 mM h(-1) for quinones. Apparent quantum yields (Θ app; measure of photochemical production efficiency) were higher for HA vs. FA (0.113 vs. 0.016) and ranged from 0.0018 to 0.083 for quinones. Dihydroquinone, the reduced form of benzoquinone, had a higher production rate and efficiency than its oxidized form. Post-irradiation, quinone compounds had absorption spectra similar to HA and FA and 3D-excitation-emission matrix fluorescence spectra (EEMs) with fluorescent peaks in regions associated with CDOM.

  7. Damage accumulation in ion-irradiated Ni-based concentrated solid-solution alloys

    DOE PAGES

    Ullah, Mohammad W.; Aidhy, Dilpuneet S.; Zhang, Yanwen; ...

    2016-03-05

    We investigate Irradiation-induced damage accumulation in Ni0.8Fe0.2 and Ni0.8Cr0.2 alloys by using molecular dynamics simulations to assess possible enhanced radiation-resistance in these face-centered cubic (fcc), single-phase, concentrated solid-solution alloys, as compared with pure fcc Ni.

  8. Impact of alloy composition on one-dimensional glide of small dislocation loops in concentrated solid solution alloys

    DOE PAGES

    Shi, Shi; Bei, Hongbin; Robertson, Ian M.

    2017-06-08

    One-dimensional glide of loops during ion irradiation at 773 K in a series of Ni-containing concentrated solid solution alloys has been observed directly during experiments conducted inside a transmission electron microscope. It was found that the frequency of the oscillatory motion of the loop, the loop glide velocity as well as the loop jump distance were dependent on the composition of the alloy and the size of the loop. Loop glide was most common for small loops and occurred more frequently in the less complex alloys, being highest in Ni, then NiCo, NiFe and NiCoFeCr. As a result, no measurablemore » loop glide occurred in the NiCoCr, NiCoFeCrMn and NiCoFeCrPd alloys.« less

  9. Corrosion behavior of electrodeposited Co-Fe alloys in aerated solutions

    NASA Astrophysics Data System (ADS)

    Chansena, A.; Sutthiruangwong, S.

    2017-05-01

    Co-Fe alloy is an important component for reader-writer in hard disk drive. The surface of the alloy is exposed to the environment both in gas phase and in liquid phase during manufacturing process. The study of corrosion behavior of Co-Fe alloys can provide useful fundamental data for reader-writer production planning especially when corrosion becomes a major problem. The corrosion study of electrodeposited Co-Fe alloys from cyclic galvanodynamic polarization was performed using potentiodynamic polarization technique. The composition of electrodeposited Co-Fe alloys was determined by X-ray fluorescence spectrometry. The patterns from X-ray diffractometer showed that the crystal structure of electrodeposited Co-Fe alloys was body-centered cubic. A vibrating sample magnetometer was used for magnetic measurements. The saturation magnetization (Ms) was increased and the intrinsic coercivity (Hci) was decreased with increasing Fe content. The corrosion rate study was performed in aerated deionized water and aerated acidic solutions at pH 3, 4 and 5. The corrosion rate diagram for Co-Fe alloys was constructed. It was found that the corrosion rate of Co-Fe alloys was increased with increasing Fe content in both aerated deionized water and aerated acidic solutions. In aerated pH 3 solution, the Co-Fe alloy containing 78.8% Fe showed the highest corrosion rate of 7.7 mm yr-1 with the highest Ms of 32.0 A m2 kg-1. The corrosion rate of the alloy with 23.8% Fe was at 1.1 mm yr-1 with Ms of 1.2 A m2 kg-1. In aerated deionized water, the alloy with the highest Fe content of 78.5% still showed the highest corrosion rate of 0.0059 mm yr-1 while the alloy with the lowest Fe content of 20.4% gave the lowest corrosion rate of 0.0045 mm yr-1.

  10. Static atomic displacements in crystalline solid solution alloys

    SciTech Connect

    Ice, G.; Sparks, C.; Robertson, J.L.; Epperson, J.E.; Jiang, Xiaogang

    1996-06-01

    Atomic size differences induce static displacements from an average alloy lattice and play an important role in controlling alloy phase stability and properties. Details of this, however, are difficult to study, as chemical order and displacements are strongly interrelated and static displacements are hard to measure. Diffuse x-ray scattering with tunable-synchrotron radiation can now measure element- specific static displacements with an accuracy of {+-}0.1 pm and can simultaneously measure local chemical order out to 20 shells or more. Ideal alloys for this are those that have previously been the most intractable: alloys with small Z contrast, alloys with only local order and alloys with small size differences. The combination of precise characterization of local chemical order and precise measurement of static displacement provides new information that challenges existing alloy models. This paper reports on an ongoing systematic study of static displacements in the Fe/Ni/Cr alloys and compares the observed static displacements to these predicted by current theories. Availability of more brilliant 3rd generation hard x-ray sources will greatly enhance these measurements.

  11. Effects of pH and dissolved oxygen on the photodegradation of 17α-ethynylestradiol in dissolved humic acid solution.

    PubMed

    Ren, Dong; Huang, Bin; Bi, Tingting; Xiong, Dan; Pan, Xuejun

    2016-01-01

    To probe the mechanisms responsible for pH and dissolved oxygen (DO) affecting the photodegradation of 17α-ethynylestradiol (EE2) in dissolved humic acid (HA) solution, EE2 aqueous solutions with pH values ranging from 3.0 to 11.0 and different DO conditions were irradiated by using a 300 W mercury lamp equipped with 290 nm light cutoff filters. In 5.0 mg L(-1) HA solutions (pH 8.0), EE2 was degraded at a rate of 0.0739 h(-1) which was about 4-fold faster than that in Milli-Q water. The degradation of EE2 was mainly caused by the oxidation of photogenerated reactive species (RS), and the contribution of direct photodegradation to EE2 degradation was always lower than 27%. Both the direct and indirect photodegradation of EE2 were closely dependent on the EE2 initial concentration, pH value and DO concentration. The photodegradation rate of EE2 decreased with increased initial concentration of EE2 due to the limitation of photon flux. With pH and DO increasing, the degradation rate of EE2 increased significantly due to the increase in the yields of excited EE2 and RS. Among the photogenerated RS, HO˙ and (3)HA* were determined to be the key contributors, and their global contribution to EE2 photodegradation was about 50%. Although HA could generate more (1)O2 than HO˙, the contribution of (1)O2 to EE2 degradation was lower than 13% due to its low reactivity towards EE2. This study could enlarge our knowledge on the photochemical behaviors of steroid estrogens in natural sunlit waters.

  12. Effect of indium (In) on corrosion and passivity of a beta-type Ti-Nb alloy in Ringer's solution

    NASA Astrophysics Data System (ADS)

    Gebert, Annett; Oswald, Steffen; Helth, Arne; Voss, Andrea; Gostin, Petre Flaviu; Rohnke, Marcus; Janek, Jürgen; Calin, Mariana; Eckert, Jürgen

    2015-04-01

    Beta-phase Ti-Nb-based alloys are considered as new generation of biomaterials with improved mechanical compatibility for load-bearing implant applications. Small homogeneously dissolved In additions have a positive impact on the elastic properties of beta-type Ti-40Nb. For (Ti-40Nb)-4In the best match between low Young's modulus, high elastic energy and appropriate strength was achieved. In the present study the effect of In addition to Ti-40Nb on the corrosion and passivation behavior in Ringer's solution is assessed by means of potentiodynamic polarization, ICP-OES metal release analysis, XPS and ToF-SIMS for passive film characterization. Like Ti-40Nb, (Ti-40Nb)-4In exhibits very low corrosion rates (icorr = 0.1-0.2 μA/cm2) and stable anodic passivity (ipass = 3-4 μA/cm2). Small In additions do not have a detectable effect on the anodic response of the alloy. For both beta-phase alloys metal release rates are below the quantification limits of ICP-OES. Their strong passivating nature is governed by the formation of thin barrier-type Ti- and Nb-oxide films. Passive films on (Ti-40Nb)-4In surfaces which were formed during OCP exposure or anodic polarization comprise oxidized In species (In2O3, In(OH3)). From the viewpoint of corrosion stability (Ti-40Nb)-4In appears to be suitable for implant applications.

  13. Hydrogen embrittlement of Ni-Ti superelastic alloy in fluoride solution.

    PubMed

    Yokoyama, Ken'ichi; Kaneko, Kazuyuki; Moriyama, Keiji; Asaoka, Kenzo; Sakai, Jun'ichi; Nagumo, Michihiko

    2003-05-01

    Hydrogen embrittlement of Ni-Ti superelastic alloy in a fluoride solution (0.2% APF) has been investigated by means of a tensile test (after immersion) and hydrogen thermal desorption analysis. Upon immersion, the tensile strength of the alloy decreased to the critical stress level of martensite transformation. Hydrogen desorption of the immersed specimens appeared with a peak at around 500 degrees C. The amount of absorbed hydrogen in the alloy ranged from 100 to 1000 mass ppm when immersed in the fluoride solution for 2 to 24 h. The immersion in the fluoride solution led to the degradation of mechanical properties due to hydrogen embrittlement. The results of the present study imply that one reason that Ti and its alloys fracture in the oral cavity is the fact that hydrogen is absorbed in a fluoride solution, such as prophylactic agents.

  14. THE ROLE OF ELECTRON CONFIGURATION ON PROPERTIES IN DILUTE SOLID SOLUTION ALLOYS

    DTIC Science & Technology

    THE ROLE OF ELECTRON CONFIGURATION ON THE PROPERTIES OF DILUTE SOLID SOLUTION ALLOYS IS DISCUSSED IN TERMS OF THE EFFECT OF DILUTE IMPURITIES ON THE RECRYSTALLIZATION CHARACTERISTICS OF PURE METALLIC ELEMENTS.

  15. An electrochemical and multispectroscopic study of corrosion of Ag-Pd-Cu-Au alloys.

    PubMed

    Niemi, L; Minni, E; Ivaska, A

    1986-06-01

    Corrosion of a multi-phase Ag-Pd-Cu-Au-based commercial dental casting alloy and a Cu-Pd-rich and Ag-rich single-phase alloy was studied by open-circuit potential measurements, atomic absorption spectrometry, and electron spectroscopy. The alloys were immersed in an artificial saliva solution for 24 hr while the open-circuit potentials of the alloys were measured. The potentials were found to stabilize at certain levels after a steep rise during the first hours of the experiment. Cu was found to dissolve considerably from the Cu-Pd-rich alloy, with simultaneous enrichment of Pd in the surface layer of the alloy. Ag dissolved slightly from the Ag-rich alloy, but both Cu and Ag were found to dissolve from the multi-phase alloy. Neither Pd nor Au dissolved from any of the alloys studied.

  16. Effects of dissolved hydrogen on general corrosion behavior and oxide films of alloy 690TT in PWR primary water

    NASA Astrophysics Data System (ADS)

    Jeon, Soon-Hyeok; Lee, Eun-Hee; Hur, Do Haeng

    2017-03-01

    The effect of dissolved hydrogen (DH) on the general corrosion behavior and oxide films of Alloy 690TT is investigated in simulated primary water at 330 °C. With increasing DH, the structure of oxide film significantly changed and the corrosion rate decreased. At DH = 5 cm3/kg H2O, the oxide layer was thick, and consisted of outer Ni oxide layer and inner Cr2O3 layer. Under the conditions of DH = 35 and 100 cm3/kg H2O, the oxide films grew thinner and composed of outer polyhedral spinel oxide particles such as NiCr2O4 or NiCrFeO4 and an intermediate metallic Ni-rich layer, with inner Cr2O3 layer. The general corrosion rate significantly decreased by about 72% as DH concentration increased from 5 to 35 cm3/kg H2O. In the range of 35-65 cm3/kg H2O, the corrosion rate slightly decreased with increasing DH concentration. However, no further changes were observed in the range of 65-100 cm3/kg H2O.

  17. Hydrogen-storage properties of solid-solution alloys of immiscible neighboring elements with Pd.

    PubMed

    Kusada, Kohei; Yamauchi, Miho; Kobayashi, Hirokazu; Kitagawa, Hiroshi; Kubota, Yoshiki

    2010-11-17

    Rh and Ag are the elements neighboring Pd, which is well known as a hydrogen-storage metal. Although Rh and Ag do not possess hydrogen-storage properties, can Ag-Rh alloys actually store hydrogen? Ag-Rh solid-solution alloys have not been explored in the past because they do not mix with each other at the atomic level, even in the liquid phase. We have used the chemical reduction method to obtain such Ag-Rh alloys, and XRD and STEM-EDX give clear evidence that the alloys mixed at the atomic level. From the measurements of hydrogen pressure-composition isotherms and solid-state (2)H NMR, we have revealed that Ag-Rh solid-solution alloys absorb hydrogen, and the total amount of hydrogen absorbed reached a maximum at the ratio of Ag:Rh = 50:50, where the electronic structure is expected to be similar to that of Pd.

  18. Electrochemical generation of hydrogen peroxide from dissolved oxygen in acidic solutions.

    PubMed

    Qiang, Zhimin; Chang, Jih-Hsing; Huang, Chin-Pao

    2002-01-01

    Hydrogen peroxide (H2O2) was electro-generated in a parallel-plate electrolyzer by reduction of dissolved oxygen (DO) in acidic solutions containing dilute supporting electrolyte. Operational parameters such as cathodic potential, oxygen purity and mass flow rate, cathode surface area. pH, temperature, and inert supporting electrolyte concentration were systematically investigated as to improve the Faradic current efficiency of H2O2 generation. Results indicate that significant self-decomposition of H2O2 only occurs at high pH (> 9) and elevated temperatures (> 23 degrees C). Results also indicate that the optimal conditions for H2O2 generation are cathodic potential of -0.5 V vs. saturated calomel electrode (SCE), oxygen mass flow rate of 8.2 x 10(-2) mol/min, and pH 2. Under the optimal conditions, the average current density and average current efficiency are 6.4A/m2 and 81%, respectively. However, when air is applied at the optimal flow rate of oxygen, the average current density markedly decreases to 2.1 A/m2, while the average current efficiency slightly increases to 90%. The limiting current density is 6.4 A/m2, which is independent of cathode geometry and surface area. H2O2 generation is favored at low temperatures. In the concentration range studied (0.01-0.25 M), the inert supporting electrolyte (NaClO4) affects the total potential drop of the electrolyzer, but does not affect the net generation rate of H2O2.

  19. Fretting properties of biodegradable Mg-Nd-Zn-Zr alloy in air and in Hank's solution.

    PubMed

    Li, Wenting; Li, Nan; Zheng, Yufeng; Yuan, Guangyin

    2016-11-04

    Fretting is a significant cause for the failure of orthopedic implants. Currently, since magnesium and its alloys have been developed as promising biodegradable implant materials, the fretting behavior of the Mg alloys is of great research significance. In this study, a Mg-Nd-Zn-Zr alloy (hereafter, denoted as JDBM alloy) was selected as experimental material, and its fretting behaviors were evaluated under 5 N, 10 N and 20 N normal loads with a displacement of 200 μm under the frequency of 10 Hz at 37 °C in air and in Hank's solution, respectively. The results indicated that while the friction coefficient decreased with the increment of the normal load, the wear volume of the alloy increased with the increment of the normal load both in air and in Hank's solution. Both the friction coefficients and the wear volume of the fretting in Hank's solution were much lower than those in air environment. The evolution trend of friction coefficients with time had different performance in air environment and the Hank's solution group. Although oxidation occurred during the fretting tests in Hank's solution, the damage of JDBM alloy was still reduced due to the lubrication effects of Hank's solution. Moreover, the addition of Fetal bovine serum (FBS) could act as lubrication and result in the reduction of the fretting damage.

  20. The effects of temperature and aeration on the corrosion of A508III low alloy steel in boric acid solutions at 25-95 °C

    NASA Astrophysics Data System (ADS)

    Xiao, Qian; Lu, Zhanpeng; Chen, Junjie; Yao, Meiyi; Chen, Zhen; Ejaz, Ahsan

    2016-11-01

    The effects of temperature, solution composition and dissolved oxygen on the corrosion rate and electrochemical behavior of an A508III low alloy steel in boric acid solution with lithium hydroxide at 25-95 °C are investigated. In aerated solutions, increasing the boric acid concentration increases the corrosion rate and the anodic current density. The corrosion rate in deaerated solutions increases with increasing temperature. A corrosion rate peak value is found at approximately 75 °C in aerated solutions. Increasing temperature increases the oxygen diffusion coefficient, decreases the dissolved oxygen concentration, accelerates the hydrogen evolution reaction, and accelerates both the active dissolution and the film forming reactions. Increasing dissolved oxygen concentration does not significantly affect the corrosion rate at 50 and 60 °C, increases the corrosion rate at 70 and 80 °C, and decreases the corrosion rate at 87.5 and 95 °C in a high concentration boric acid solution with lithium hydroxide.

  1. The coupled effect of grain size and solute on work hardening of Cu-Ni alloys

    NASA Astrophysics Data System (ADS)

    Shadkam, A.; Sinclair, C. W.

    2015-12-01

    A modified grain size-dependent model developed to capture the combined effects of solute and grain size on the work hardening behaviour of fine-grained Cu-Ni alloys is provided. This work builds on a recent model that attributes the grain size-dependent work hardening of fine-grained Cu to backstresses. In the case of Cu-Ni alloys, unlike commercially pure Cu, a grain size-dependent separation between the Kocks-Mecking curves develops, this being explained here based on an extra contribution from geometrically necessary dislocations in the solid solution alloy. This is corroborated by strain-rate sensitivity experiments.

  2. Structurally colored biopolymer thin films for detection of dissolved metal ions in aqueous solution

    NASA Astrophysics Data System (ADS)

    Cathell, Matthew David

    Natural polymers, such as the polysaccharides alginate and chitosan, are noted sorbents of heavy metals. Their polymer backbone structures are rich in ligands that can interact with metal ions through chelation, electrostatics, ion exchange and nonspecific mechanisms. These water-soluble biopolymer materials can be processed into hydrogel thin films, creating high surface area interfaces ideal for binding and sequestering metal ions from solution. By virtue of their uniform nanoscale dimensions (with thicknesses smaller than wavelengths of visible light) polymer thin films exhibit structure-based coloration. This phenomenon, frequently observed in nature, causes the transparent and essentially colorless films to reflect light in a wide array of colors. The lamellar film structures act as one-dimensional photonic crystals, allowing selective reflection of certain wavelengths of light while minimizing other wavelengths by out-of-phase interference. The combination of metal-binding and reflective properties make alginate and chitosan thin films attractive candidates for analyte sensing. Interactions with metal ions can induce changes in film thicknesses and refractive indices, thus altering the path of light reflected through the film. Small changes in dimensional or optical properties can lead to shifts in film color that are perceivable by the unaided eye. These thin films offer the potential for optical sensing of toxic dissolved materials without the need for instrumentation, external power or scientific expertise. With the use of a spectroscopic ellipsometer and a fiber optic reflectance spectrometer, the physical and optical characteristics of biopolymer thin films have been characterized in response to 50 ppm metal ion solutions. It has been determined that metal interactions can lead to measurable changes in both film thicknesses and effective refractive indices. The intrinsic response behaviors of alginate and chitosan, as well as the responses of modified

  3. ON THE DIFFUSION OF A SOLUTE IN SUBSTITUTIONAL ALLOYS

    DTIC Science & Technology

    A calculation is submitted of the diffusion coefficient of atoms which have penetrated into the internodes of body - centered cubic crystalline lattice of a binary alloy which may be in an ordered state.

  4. K Basin Sludge Conditioning Process Testing Partitioning of PCBs in Dissolver Solution After Neutralization/Precipitation (Caustic Adjustment)

    SciTech Connect

    Schmidt, A.J.; Thornton, B.M.; Hoppe, E.W.; Mong, G.M.; Silvers, K.L.; Slate, S.O.

    1999-01-04

    The purpose of the work described in this report was to gain a better understanding of how PCB congeners present in a simulated K Basin sludge dissolver solution will partition upon neutralization and precipitation (i.e., caustic adjustment). In a previous study (Mong et al. 1998),the entire series of sludge conditioning steps (acid dissolution, filtration, and caustic adjustment) were examined during integrated testing. In the work described here, the caustic adjustment step was isolated to examine the fate of PCBs in more detail within this processing step. For this testing, solutions of dissolver simulant (containing no solids) with a known initial concentration of PCB congeners were neutralized with caustic to generate a clarified supernatant and a settled sludge phase. PCBs were quantified in each phase (including the PCBs associated with the test vessel rinsates), and material balance information was collected.

  5. Dissolved and particulate Barium in the Ganga (Hooghly) River estuary, India: Solute-particle interactions and the enhanced dissolved flux to the oceans

    NASA Astrophysics Data System (ADS)

    Samanta, Saumik; Dalai, Tarun K.

    2016-12-01

    In this study, the sources and the cycling of Ba have been evaluated in the Ganga (Hooghly) River estuary using the composition of the suspended sediments and the water samples collected during six seasons of contrasting water discharge over two years (2012 and 2013). In addition, the data on the samples of groundwater from areas adjacent to the estuary, and the industrial effluent water and urban wastewater draining into the estuary are presented. Selective extraction experiments were also performed on the suspended particulate matter of two seasons to assess the distribution of exchangeable concentrations of major ions and Ba. In the mixing zone, the variation patterns of the dissolved Ba concentrations show mid-salinity maxima and are similar to the patterns of variation of the particulate Mg/Al and Mg/Fe, suggesting that the production of dissolved Ba is linked to the adsorption of major ions on to the clay minerals and Fe-Mn oxyhydroxides in the particulate matter. The inference of coupled adsorption-desorption processes is supported by the observations that the particulate Ba/Mg and Ba/K ratios exhibit significant to strong negative correlations with the concentrations of Al, Fe and Mn. The observations of mid-salinity maxima for the concentrations of exchangeable Mg and K, and of the exchangeable Ba concentrations that decrease with salinity provide strong evidence that the solute-particle interactions is the major driver in regulating the dissolved Ba distributions in the estuary. The estimates of the quantity of desorbed Ba based on three different approaches suggest that desorption is sufficient to account for the calculated excess Ba (Baxs) concentrations. The contribution of Ba to the dissolved load via dissolution of the particulate carbonate phases is minor, up to 3% of the maximum Baxs concentrations. The estimates of anthropogenic contributions are insignificant, and account for ⩽2% of maximum Baxs in the estuary. Groundwater contributions are

  6. Corrosion Behavior of Alloy 22 in Oxalic Acid and Sodium Chloride Solutions

    SciTech Connect

    Day, S D; Whalen, M T; King, K J; Hust, G A; Wong, L L; Estill, J C; Rebak, R B

    2003-06-24

    Nickel based Alloy 22 (NO6022) is extensively used in aggressive industrial applications, especially due to its resistance to localized corrosion and stress corrosion cracking in high chloride environments. The purpose of this work was to characterize the anodic behavior of Alloy 22 in oxalic acid solution and to compare its behavior to sodium chloride (NaCl) solutions. Standard electrochemical tests such as polarization resistance and cyclic polarization were used. Results show that the corrosion rate of Alloy 22 in oxalic acid solutions increased rapidly as the temperature and the acid concentration increased. Extrapolation studies show that even at a concentration of 10{sup -4}M oxalic acid, the corrosion rate of Alloy 22 would be higher in oxalic acid than in 1 M NaCl solution. Alloy 22 was not susceptible to localized corrosion in oxalic acid solutions. Cyclic polarization tests in 1 M NaCl showed that Alloy 22 was susceptible to crevice corrosion at 90 C but was not susceptible at 60 C.

  7. Biocorrosion properties of antibacterial Ti-10Cu sintered alloy in several simulated biological solutions.

    PubMed

    Liu, Cong; Zhang, Erlin

    2015-03-01

    Ti-10Cu sintered alloy has shown strong antibacterial properties against S. aureus and E. coli and good cell biocompatibility, which displays potential application in dental application. The corrosion behaviors of the alloy in five different simulated biological solutions have been investigated by electrochemical technology, surface observation, roughness measurement and immersion test. Five different simulated solutions were chosen to simulate oral condition, oral condition with F(-) ion, human body fluids with different pH values and blood system. It has been shown that Ti-10Cu alloy exhibits high corrosion rate in Saliva pH 3.5 solution and Saliva pH 6.8 + 0.2F solution but low corrosion rate in Hank's, Tyrode's and Saliva pH 6.8 solutions. The corrosion rate of Ti-10Cu alloy was in a order of Hank's, Tyrode's, Saliva pH 6.8, Saliva-pH 3.5 and Saliva pH 6.8 + 0.2F from slow to fast. All results indicated acid and F(-) containing conditions prompt the corrosion reaction of Ti-Cu alloy. It was suggested that the Cu ion release in the biological environments, especially in the acid and F(-) containing condition would lead to high antibacterial properties without any cell toxicity, displaying wide potential application of this alloy.

  8. Facile synthesis of dendritic Cu by electroless reaction of Cu-Al alloys in multiphase solution

    NASA Astrophysics Data System (ADS)

    Wang, Ying; Liang, Shuhua; Yang, Qing; Wang, Xianhui

    2016-11-01

    Two-dimensional nano- or micro-scale fractal dendritic coppers (FDCs) were synthesized by electroless immersing of Cu-Al alloys in hydrochloric acid solution containing copper chloride without any assistance of template or surfactant. The FDC size increases with the increase of Al content in Cu-Al alloys immersed in CuCl2 + HCl solution. Compared to Cu40Al60 and Cu45Al55 alloys, the FDC shows hierarchical distribution and homogeneous structures using Cu17Al83 alloy as the starting alloy. The growth direction of the FDC is <110>, and all angles between the trunks and branches are 60°. Nanoscale Cu2O was found at the edge of FDC. Interestingly, nanoporous copper (NPC) can also be obtained through Cu17Al83 alloy. Studies showed that the formation of FDC depended on two key factors: the potential difference between CuAl2 intermetallic and α-Al phase of dual-phase Cu-Al alloys; a replacement reaction that usually occurs in multiphase solution. The electrochemical experiment further proved that the multi-branch dendritic structure is very beneficial to the proton transfer in the process of catalyzing methanol.

  9. Crystal Growth of Solid Solution HgCdTe Alloys

    NASA Technical Reports Server (NTRS)

    Lehoczky, Sandor L.

    1997-01-01

    The growth of homogenous crystals of HgCdTe alloys is complicated by the large separation between their liquidus and solidus temperatures. Hg(1-x)Cd(x)Te is representative of several alloys which have electrical and optical properties that can be compositionally tuned for a number of applications. Limitations imposed by gravity during growth and results from growth under reduced conditions are described. The importance of residual accelerations was demonstrated by dramatic differences in compositional distribution observed for different attitudes of the space shuttle that resulted in different steady acceleration components.

  10. Crystal Growth of Solid Solution HgCdTe Alloys

    NASA Technical Reports Server (NTRS)

    Lehoczky, Sandor L.

    1997-01-01

    The growth of homogenous crystals of HgCdTe alloys is complicated by the large separation between their liquidus and solidus temperatures. Hg(1-x)Cd(x)Te is representative of several alloys which have electrical and optical properties that can be compositionally tuned for a number of applications. Limitations imposed by gravity during growth and results from growth under reduced conditions are described. The importance of residual accelerations was demonstrated by dramatic differences in compositional distribution observed for different attitudes of the space shuttle that resulted in different steady acceleration components.

  11. Extraction equilibrium of indium(III) from nitric acid solutions by di(2-ethylhexyl)phosphoric acid dissolved in kerosene.

    PubMed

    Tsai, Hung-Sheng; Tsai, Teh-Hua

    2012-01-04

    The extraction equilibrium of indium(III) from a nitric acid solution using di(2-ethylhexyl) phosphoric acid (D2EHPA) as an acidic extractant of organophosphorus compounds dissolved in kerosene was studied. By graphical and numerical analysis, the compositions of indium-D2EHPA complexes in organic phase and stoichiometry of the extraction reaction were examined. Nitric acid solutions with various indium concentrations at 25 °C were used to obtain the equilibrium constant of InR₃ in the organic phase. The experimental results showed that the extraction distribution ratios of indium(III) between the organic phase and the aqueous solution increased when either the pH value of the aqueous solution and/or the concentration of the organic phase extractant increased. Finally, the recovery efficiency of indium(III) in nitric acid was measured.

  12. Bounds to Hardening by Solid Solution, Precipitation and Short Range Order in Mg Binary Alloys

    NASA Astrophysics Data System (ADS)

    Cáceres, C. H.; Abaspour, Saeideh

    Miedema's coordinates are used to rank 4 model binary alloys considering the respective values of enthalpy of formation and the tendency to developing random solid solution, precipitation, short range order (SRO) and intermetallic compounds. The terminal solid solubility generally increases whereas the tendency to order decreases with decreasing heat of formation, and hardening by near-random solid solution and/or precipitation is expected to be dominant for solutes with low tendency to order, such as Al. For solutes with an intermediate tendency to order, hence solubility, such as Zn, or to form compounds, such as Gd, SRO is predicted to dominate the hardening. For solutes whose very large heat of formation leads to very high melting point intermetallics forming congruently, such as Sb, the terminal solid solubility is too low for any solute based hardening to be feasible. Implicancies for alloy design and selection regarding solute or precipitation hardening, SRO and creep resistance are discussed.

  13. Effects of progressive solution treatment on microstructure and property of the aluminium alloy electrical round rod

    NASA Astrophysics Data System (ADS)

    Hu, Xiejun; Zhang, Renguo; Zhang, Xiaoyan; Lin, Tingyi; Zhang, Junjie; Yan, Jun

    2017-06-01

    This paper aims to research the effects of progressive solution treatment on property of aluminium alloy electrical round rod, we mainly research the influences of different temperature on tensile strength and electrical conductivity of the aluminium alloy electrician round rod. The component and phase constitution of the aluminium alloy was analysed by means of OLYMPUSPMG-3 horizontal metallurgical microscope, SUPRA40 scanning electron microscope, APOLLO-10Xenergy spectrometer, tensile strength and conductivity of aluminium alloy electrical round rod under various progressive solution treatment. The results show that: comprehensive performance of specimen is optimal by means of scheme(350 °C×1h+510°C×6h), the conductivity is 56.6%IACS and the tensile strength is 103MPa.

  14. Influence of chemical disorder on energy dissipation and defect evolution in concentrated solid solution alloys

    SciTech Connect

    Zhang, Yanwen; Stocks, George Malcolm; Jin, Ke; Lu, Chenyang; Bei, Hongbin; Sales, Brian C.; Wang, Lumin; Béland, Laurent K.; Stoller, Roger E.; Samolyuk, German D.; Caro, Magdalena; Caro, Alfredo; Weber, William J.

    2015-10-28

    A long-standing objective in materials research is to understand how energy is dissipated in both the electronic and atomic subsystems in irradiated materials, and how related non-equilibrium processes may affect defect dynamics and microstructure evolution. Here we show that alloy complexity in concentrated solid solution alloys having both an increasing number of principal elements and altered concentrations of specific elements can lead to substantial reduction in the electron mean free path and thermal conductivity, which has a significant impact on energy dissipation and consequentially on defect evolution during ion irradiation. Enhanced radiation resistance with increasing complexity from pure nickel to binary and to more complex quaternary solid solutions is observed under ion irradiation up to an average damage level of 1 displacement per atom. Understanding how materials properties can be tailored by alloy complexity and their influence on defect dynamics may pave the way for new principles for the design of radiation tolerant structural alloys.

  15. Approximate solutions for diffusive fracture-matrix transfer: Application to storage of dissolved CO2 in fractured rocks

    DOE PAGES

    Zhou, Quanlin; Oldenburg, Curtis M.; Spangler, Lee H.; ...

    2017-01-05

    Analytical solutions with infinite exponential series are available to calculate the rate of diffusive transfer between low-permeability blocks and high-permeability zones in the subsurface. Truncation of these series is often employed by neglecting the early-time regime. Here in this paper, we present unified-form approximate solutions in which the early-time and the late-time solutions are continuous at a switchover time. The early-time solutions are based on three-term polynomial functions in terms of square root of dimensionless time, with the first coefficient dependent only on the dimensionless area-to-volume ratio. The last two coefficients are either determined analytically for isotropic blocks (e.g., spheresmore » and slabs) or obtained by fitting the exact solutions, and they solely depend on the aspect ratios for rectangular columns and parallelepipeds. For the late-time solutions, only the leading exponential term is needed for isotropic blocks, while a few additional exponential terms are needed for highly anisotropic rectangular blocks. The optimal switchover time is between 0.157 and 0.229, with highest relative approximation error less than 0.2%. The solutions are used to demonstrate the storage of dissolved CO2 in fractured reservoirs with low-permeability matrix blocks of single and multiple shapes and sizes. These approximate solutions are building blocks for development of analytical and numerical tools for hydraulic, solute, and thermal diffusion processes in low-permeability matrix blocks.« less

  16. Dissolved oxygen distribution during micro-oxygenation. Determination of representative measurement points in hydroalcoholic solution and wines.

    PubMed

    Nevares, I; del Alamo, M; Gonzalez-Muñoz, C

    2010-02-15

    Red wine tank aging is monitored by organoleptic analysis, therefore, it is necessary to use an objective parameter representing the process. Among the possible parameters to be checked, it stands out the knowledge of dissolved oxygen because it offers the possibility of anticipating undesirable situations that bring about too much oxidation. Dissolved oxygen measurement, with non-intrusive luminescent technology is becoming an effective alternative. Uncertainty arises when trying to choose the measuring point able to represent the entire tank since previous works have considered the existence of gradients throughout the volume of the treated wine. This paper shows the results obtained from the study of the existence and the quantification of gradients of the dissolved oxygen in a 15% hydroalcoholic solution during the micro-oxygenation process. Different measuring point placements are studied and the solutions to monitor the process by controlling a representative point are set out. A successful monitoring of a red wine tank aging with alternative oak products and adaptative micro-oxygenation has proved that an objective control of the process is, indeed, possible.

  17. Electrochemical Corrosion Behavior of Borided CoCrMo Alloy Immersed in Hanks' Solution

    NASA Astrophysics Data System (ADS)

    Rosas-Becerra, G.; Mejía-Caballero, I.; Martínez-Trinidad, J.; Palomar-Pardavé, M.; Romero-Romo, M.; Pérez-Pasten-Borja, R.; Campos-Silva, I.

    2017-02-01

    New results about the corrosion resistance of borided CoCrMo alloy exposed to the Hanks' solution during different days were estimated by means of the electrochemical impedance spectroscopy technique. The CoB-Co2B coating was developed on the surface of the borided alloy using the powder-pack boriding process at 1223 K during 6 h of exposure. The corrosion resistance of the borided cobalt alloy was evaluated by the fitting of suitable equivalent electrical circuits using Nyquist and Bode plots to obtain the electrochemical parameters; the results were compared with the CoCrMo (non-borided) alloy. The samples (borided and non-borided) were characterized by the scanning electron microscopy and by the energy-dispersive x-ray spectrometry techniques to determine the elemental chemical composition developed on the surface of the materials. In addition, the reaction products formed on the surface of the borided CoCrMo alloy exposed to the Hanks' solution after the tenth day of immersion were analyzed by the x-ray photoelectron spectroscopy (XPS) technique. The results showed that the corrosion resistance of the borided cobalt alloy was affected (or reduced) by the presence of B2S3 and CrPO4 clusters formed on the material's surface. Finally, the electrochemical reactions developed during the immersion of the borided cobalt alloy on the tenth day of exposure were proposed according to the XPS results.

  18. Response of solute and precipitation-strengthened copper alloys at high neutron exposure

    SciTech Connect

    Garner, F.A.; Hamilton, M.L. ); Shikama, T. ); Edwards, D.J.; Newkirk, J.W. )

    1991-11-01

    A variety of solute and precipitation strengthened copper base alloys have been irradiated to neutron-induced displacement levels of 34 to 150 dpa at 415{degrees}C and 32 dpa at 529{degrees}C in the Fast Flux Test Facility to assess their potential for high heat flux applications in fusion reactors. Several MZC-type alloys appear to offer the most promise for further study. For low fluence applications CuBeNi and spinodally strengthened CuNiTi alloys may also be suitable. Although Cu-2Be resists swelling, it is not recommended for fusion reactor applications because of its low conductivity.

  19. Saturation magnetization in supersaturated solid solution of Co-Cu alloy

    NASA Astrophysics Data System (ADS)

    Yuasa, Motohiro; Kajikawa, Kota; Hakamada, Masataka; Mabuchi, Mamoru

    2009-10-01

    The magnetovolume effect has been investigated using a supersaturated solid solution of a Co-19 at. %Cu alloy processed by electrodeposition. The enhanced saturation magnetization of the Co-Cu alloy was attributed to both metastable fcc Co and lattice expansion. The density functional theory using the CASTEP code revealed that an enhanced magnetic moment due to the magnetovolume effect is obtained in fcc Co, but not in hcp Co.

  20. Damage accumulation in ion-irradiated Ni-based concentrated solid-solution alloys

    SciTech Connect

    Ullah, Mohammad W.; Aidhy, Dilpuneet S.; Zhang, Yanwen; Weber, William J.

    2016-01-01

    We investigate Irradiation-induced damage accumulation in Ni0.8Fe0.2 and Ni0.8Cr0.2 alloys by using molecular dynamics simulations to assess possible enhanced radiation-resistance in these face-centered cubic (fcc), single-phase, concentrated solid-solution alloys, as compared with pure fcc Ni.

  1. Reclamation of cadmium-contaminated soil using dissolved organic matter solution originating from wine-processing waste sludge.

    PubMed

    Liu, Cheng-Chung; Chen, Guan-Bu

    2013-01-15

    Soil washing using an acid solution is a common practice for removing heavy metals from contaminated soil in Taiwan. However, serious loss of nutrients from soil is a major drawback of the washing. Distillery sludge can be used to prepare a dissolved organic matter (DOM) solution by extracting its organic constituents with alkaline solutions. This study employed DOM solutions to remediate Cd-contaminated soil (with concentrations up to 21.5 mg kg(-1)) and determine the factors affecting removal of Cd, such as pH, initial concentration of DOM solution, temperature, and washing frequency. When washing with pH 3.0 and 1250 mg L(-1) DOM solution, about 80% and 81% of Cd were removed from the topsoil at 27 °C and subsoil at 40 °C, respectively. To summarize the changes in fertility during DOM washing with various pH solutions: the increase in organic matter content ranged from 7.7% to 23.7%; cation exchange capacity (CEC) ranged from 4.6% to 13.9%; available ammonium (NNH(4)) content ranged from 39.4% to 2175%; and available phosphorus content ranged from 34.5% to 182%. Exchangeable K, Ca, and Mg remained in the topsoil after DOM washing, with concentrations of 1.1, 2.4, and 1.5 times higher than those treated with HCl solution at the same pH, respectively. Copyright © 2012 Elsevier B.V. All rights reserved.

  2. Delayed fracture of Ni-Ti superelastic alloys in acidic and neutral fluoride solutions.

    PubMed

    Yokoyama, Ken'ichi; Kaneko, Kazuyuki; Moriyama, Keiji; Asaoka, Kenzo; Sakai, Jun'ichi; Nagumo, Michihiko

    2004-04-01

    Hydrogen-related degradation of the mechanical properties of a Ni-Ti superelastic alloy has been examined by means of delayed fracture tests in acidic and neutral fluoride solutions and hydrogen thermal desorption analysis. Delayed fracture took place in both solutions; the time to fracture was shorter in the acidic solutions than in the neutral solutions with the same fluoride concentration. The time to fracture was reduced in both solutions when applied stress exceeded the critical stress for martensite transformation. In the acidic solutions, Ni-Ti superelastic alloy underwent general corrosion and absorbed substantial amounts of hydrogen. Fractographic features suggested that the delayed fracture in the acidic solutions was attributable to hydrogen embrittlement, whereas in the neutral solutions, a different fracture mode appeared associated with localized corrosion only in the vicinity of the fracture initiation area. In the neutral solutions, the amount of absorbed hydrogen was much less than that in the acidic solutions, and the delayed fracture was likely to be induced by active path corrosion accompanying hydrogen absorption. The results of the present study imply that the hydrogen-related degradation of performance of Ni-Ti superelastic alloys occurs in the presence of fluoride.

  3. Surface corrosion enhancement of passive films on NiTi shape memory alloy in different solutions.

    PubMed

    Jinlong, Lv; Tongxiang, Liang; Chen, Wang; Limin, Dong

    2016-06-01

    The corrosion behaviors of NiTi shape memory alloy in NaCl solution, H2SO4 solution and borate buffer solution were investigated. It was found that TiO2 in passive film improved the corrosion resistance of NiTi shape memory. However, low corrosion resistance of passive film was observed in low pH value acidic solution due to TiO2 dissolution. Moreover, the corrosion resistance of NiTi shape memory alloy decreased with the increasing of passivated potential in the three solutions. The donor density in passive film increased with the increasing of passivated potential. Different solutions affect the semiconductor characteristics of the passive film. The reducing in the corrosion resistance was attributed to the more donor concentrations in passive film and thinner thickness of the passive film. Copyright © 2016 Elsevier B.V. All rights reserved.

  4. Corrosion-wear behavior of nanocrystalline Fe88Si12 alloy in acid and alkaline solutions

    NASA Astrophysics Data System (ADS)

    Fu, Li-cai; Qin, Wen; Yang, Jun; Liu, Wei-min; Zhou, Ling-ping

    2017-01-01

    The corrosion-wear behavior of a nanocrystalline Fe88Si12 alloy disc coupled with a Si3N4 ball was investigated in acid (pH 3) and alkaline (pH 9) aqueous solutions. The dry wear was also measured for reference. The average friction coefficient of Fe88Si12 alloy in the pH 9 solution was approximately 0.2, which was lower than those observed for Fe88Si12 alloy in the pH 3 solution and in the case of dry wear. The fluctuation of the friction coefficient of samples subjected to the pH 9 solution also showed similar characteristics. The wear rate in the pH 9 solution slightly increased with increasing applied load. The wear rate was approximately one order of magnitude less than that in the pH 3 solution and was far lower than that in the case of dry wear, especially at high applied load. The wear traces of Fe88Si12 alloy under different wear conditions were examined and analyzed by scanning electron microscopy, energy-dispersive X-ray spectroscopy, and X-ray photoelectron spectroscopy. The results indicated that the tribo-chemical reactions that involve oxidation of the worn surface and hydrolysis of the Si3N4 ball in the acid solution were restricted in the pH 9 aqueous solution. Thus, water lubrication can effectively improve the wear resistance of nanocrystalline Fe88Si12 alloy in the pH 9 aqueous solution.

  5. Solution softening in magnesium alloys: the effect of solid solutions on the dislocation core structure and nonbasal slip.

    PubMed

    Tsuru, T; Udagawa, Y; Yamaguchi, M; Itakura, M; Kaburaki, H; Kaji, Y

    2013-01-16

    There is a pressing need to improve the ductility of magnesium alloys so that they can be applied as lightweight structural materials. In this study, a mechanism for enhancing the ductility of magnesium alloys has been pursued using the atomistic method. The generalized stacking fault (GSF) energies for basal and prismatic planes in magnesium were calculated by using density functional theory, and the effect of the GSF energy on the dislocation core structures was examined using a semidiscrete variational Peierls-Nabarro model. Yttrium was found to have an anomalous influence on the solution softening owing to a reduction in the GSF energy gradient.

  6. Structural and magnetic properties of mechanically alloyed Co 20Cu 80 solid solution

    NASA Astrophysics Data System (ADS)

    Yoo, Y. G.; Yang, D. S.; Yu, S. C.; Kim, W. T.; M. Lee, J.

    1999-08-01

    Microstructural change during the mechanical alloying of Co 20Cu 80 has been studied by X-ray diffractometry (XRD) and extended X-ray absorption fine structure (EXAFS) techniques. EXAFS analysis shows clearly the formation of supersaturated Co 20Cu 80 solid solution with FCC crystal structure during mechanical alloying, which is in good agreement with XRD analysis. Magnetic properties also have been studied by SQUID magnetometer from 4 to 290 K. The supersaturated Co 20Cu 80 solid solution shows wide distribution in Co cluster size due to the continuous blocking of Co cluster as a function of temperature.

  7. Preparation of Ultrafine Fe-Pt Alloy and Au Nanoparticle Colloids by KrF Excimer Laser Solution Photolysis.

    PubMed

    Watanabe, Masato; Takamura, Hitoshi; Sugai, Hiroshi

    2009-03-10

    We prepared ultrafine Fe-Pt alloy nanoparticle colloids by UV laser solution photolysis (KrF excimer laser of 248 nm wavelength) using precursors of methanol solutions into which iron and platinum complexes were dissolved together with PVP dispersant to prevent aggregations. From TEM observations, the Fe-Pt nanoparticles were found to be composed of disordered FCC A1 phase with average diameters of 0.5-3 nm regardless of the preparation conditions. Higher iron compositions of nanoparticles require irradiations of higher laser pulse energies typically more than 350 mJ, which is considered to be due to the difficulty in dissociation of Fe(III) acetylacetonate compared with Pt(II) acetylacetonate. Au colloid preparation by the same method was also attempted, resulting in Au nanoparticle colloids with over 10 times larger diameters than the Fe-Pt nanoparticles and UV-visible absorption peaks around 530 nm that originate from the surface plasmon resonance. Differences between the Fe-Pt and Au nanoparticles prepared by the KrF excimer laser solution photolysis are also discussed.

  8. Simultaneous Measurement of Dissolved Oxygen Pressure and Oxyhemoglobin Spectra in Solution.

    PubMed

    Litorja, Maritoni; Hwang, Jeeseong C

    2016-01-01

    The measurement of the spatial distribution of oxygen saturation (sO2) in superficial tissues using optical reflectance imaging has been useful in the clinical venue especially in temporally demanding applications such as monitoring tissue oxygenation during surgery. The measurement is based on relative spectrometry of oxy- and deoxyhemoglobin in tissues. We titrated deoxyhemoglobin with oxygen gas and simultaneously measured the dissolved oxygen pressure and the visible absorbance spectra to verify spectral shapes at different saturations. sO2 values derived from the measured pO2 are compared to those derived from the hemoglobin spectra at various stages of oxygenation.

  9. Point defect induced segregation of alloying solutes in α-Fe

    NASA Astrophysics Data System (ADS)

    You, Yu-Wei; Zhang, Yange; Li, Xiangyan; Xu, Yichun; Liu, C. S.; Chen, J. L.; Luo, G.-N.

    2016-10-01

    Segregation of alloying solute toward clusters and precipitates can result in hardening and embrittlement of ferritic and ferritic/martensitic steels in aging nuclear power plants. Thus, it is essential to study the segregation of solute in α-Fe. In this study, the segregation of eight kinds of alloying solutes (Al, Si, P, S, Ga, Ge, As, Se) in defect-free system and at vacancy, divacancy, and self-interstitial atom in α-Fe has been systematically studied by first-principles calculations. We find that it is energetically favorable for multiple solute S or Se atoms to segregate in defect-free system to form solute clusters, whereas it is very difficult for the other solute atoms to form the similar clusters. With the presence of vacancy and divacancy, the segregation of all the solutes are significantly promoted to form vacancy-solute and divacancy-solute clusters. The divacancy-solute cluster is more stable than the vacancy-solute cluster. The most-stable self-interstitial atom <110> dumbbell is also found to tightly bind with multiple solute atoms. The <110>-S is even more stable than divacancy-S cluster. Meanwhile, the law of mass action is employed to predict the concentration evolution of vacancy-Si, vacancy-P, and vacancy-S clusters versus temperature and vacancy concentration.

  10. The Effective Diffusion Coefficient of Dissolved Oxygen and Oxidation Rate of Pyrite by Dissolved Oxygen in Compacted Purified and Crude Sodium Bentonites in Carbonate Buffered Solution

    SciTech Connect

    Manaka, Mitsuo

    2003-09-15

    Immediately after the geological disposal of high-level radioactive waste, the oxygen initially existing in the repository is expected to strongly affect the redox condition of the near field. The oxygen dissolves in the groundwater, is transported by diffusion through it, and is consumed by the oxidation of pyrite as an impurity in bentonite. To assess the influence of the oxygen, this study was conducted to estimate the diffusion of dissolved oxygen (DO) and the rate of pyrite oxidation by DO in compacted purified and crude sodium bentonites (SBs) in more detail than the Manaka et al. study. The effective diffusion coefficient (De) of DO in the compacted purified SB was measured in low ionic strength solution (carbonate buffered solution with pH {approx} 9) using the electrochemical method. The empirical equation between De value of DO and dry density (0.5 x 10{sup 3}-1.8 x 10{sup 3} kg m{sup -3}) of purified SB was obtained as follows:De{sub DO}{sup Kunipia-F} = 8.2 {+-} 1.5 x 10{sup -10}x exp(-2.6 {+-} 0.2 x10{sup -3}{rho},where De{sub DO}{sup Kunipia-F} is the De of DO in compacted purified SB (Kunipia F) (m{sup 2} s{sup -1}) and {rho} is the dry density of the SB (kg m{sup -3}).On the other hand, the De value of DO in the compacted crude SB was estimated using the relationship between De values of tritiated water in compacted purified and crude SBs. The empirical equation between the De value of DO and dry density (0.5 x 10{sup 3}-1.8 x 10{sup 3} kg m{sup -3}) of crude SB was derived as follows:De{sub DO}{sup Kunigel-V1} = 2.04 x 10{sup -9} exp(-2.6 x 10{sup -3}{rho}),where De{sub DO}{sup Kunigel-V1} is the De of DO in compacted crude SB (Kunigel V1) (m{sup 2} s{sup -1}) and {rho} is the dry density of the SB (kg m{sup -3}).The rates of pyrite oxidation by DO were estimated from the experimental data in pyrite-purified SB systems using the obtained De values of DO. The relation between rate constant (k') of pyrite oxidation by DO and dry density ({rho}) of

  11. Effects of pore size and dissolved organic matters on diffusion of arsenate in aqueous solution.

    PubMed

    Wang, Yulong; Wang, Shaofeng; Wang, Xin; Jia, Yongfeng

    2017-02-01

    Presented here is the influence of membrane pore size and dissolved organic matters on the diffusion coefficient (D) of aqueous arsenate, investigated by the diffusion cell method for the first time. The pH-dependent diffusion coefficient of arsenate was determined and compared with values from previous studies; the coefficient was found to decrease with increasing pH, showing the validity of our novel diffusion cell method. The D value increased dramatically as a function of membrane pore size at small pore sizes, and then increased slowly at pore sizes larger than 2.0μm. Using the ExpAssoc model, the maximum D value was determined to be 11.2565×10(-6)cm(2)/sec. The presence of dissolved organic matters led to a dramatic increase of the D of arsenate, which could be attributed to electrostatic effects and ionic effects of salts. These results improve the understanding of the diffusion behavior of arsenate, especially the important role of various environmental parameters in the study and prediction of the migration of arsenate in aquatic water systems.

  12. Dynamics of solutes and dissolved oxygen in shallow urban groundwater below a stormwater infiltration basin.

    PubMed

    Datry, T; Malard, F; Gibert, J

    2004-08-15

    Artificial recharge of urban aquifers with stormwater has been used extensively in urban areas to dispose of stormwater and compensate for reduced groundwater recharge. However, stormwater-derived sediments accumulating in infiltration beds may act as a source of dissolved contaminants for groundwater. Concentrations of hydrocarbons, heavy metals, nutrients and dissolved oxygen (DO) were monitored at multiple depths in shallow groundwater below a stormwater infiltration basin retaining large amounts of contaminated organic sediments. Multilevel wells and multiparameter loggers were used to examine changes in groundwater chemistry occurring over small spatial and temporal scales. Rainfall events produced a plume of low-salinity stormwater in the first 2 m below the groundwater table, thereby generating steep vertical physico-chemical gradients that resorbed during dry weather. Heavy metals and hydrocarbons were below reference concentrations in groundwater and aquifer sediments, indicating that they remained adsorbed onto the bed sediments. However, mineralization of organic sediments was the most probable cause of elevated concentrations of phosphate and DOC in groundwater. DO supply in groundwater was severely limited by bed respiration which increased with temperature. Cold winter stormwater slightly re-oxygenated groundwater, whereas warm summer stormwater lowered DO concentrations in groundwater. Among several results provided by this study, it is recommended for management purposes that infiltration practices should minimize the contact between inflow stormwater and organic sediments retained in infiltration basins.

  13. Fabrication of the supersaturated solid solution of carbon in copper by mechanical alloying

    SciTech Connect

    Liu Xueran; Liu Yongbing; Ran Xu; An Jian; Cao Zhanyi . E-mail: caozy@jlu.edu.cn

    2007-06-15

    Mechanical alloying of powder mixtures of copper and graphite was performed in a high energy ball mill. The as-milled powder was characterized by scanning electron microscopy, transmission electron microscopy, X-ray diffraction and X-ray photoelectron spectroscopy, respectively. These investigations indicated that high energy ball milling could largely extend the solid solubility of carbon in copper and the 4 wt.% C was dissolved in Cu. It was ascribed to the decrease of the grain size and the increase of the lattice strain. Nanostructures, amorphous carbon and lamellar graphite were observed in the as-milled powder after milling for 24 h.

  14. Study of Decomposition of a Highly Supersaturated Solid Solution of a Granulated Alloy, Al-1, 5Cr-1, 5Zr,

    DTIC Science & Technology

    The mechanism and kinetics of decomposition of a highly supersaturated solid solution in an alloy is of importance in stating the proper technology...that during annealing up to 250 C, there is a great density of dislocations. A hypothesis is presented concerning the structural changes occurring at heating the highly supersaturated solid solution of this alloy.

  15. Influence of chemical disorder on energy dissipation and defect evolution in concentrated solid solution alloys

    PubMed Central

    Zhang, Yanwen; Stocks, G. Malcolm; Jin, Ke; Lu, Chenyang; Bei, Hongbin; Sales, Brian C.; Wang, Lumin; Béland, Laurent K.; Stoller, Roger E.; Samolyuk, German D.; Caro, Magdalena; Caro, Alfredo; Weber, William J.

    2015-01-01

    A grand challenge in materials research is to understand complex electronic correlation and non-equilibrium atomic interactions, and how such intrinsic properties and dynamic processes affect energy transfer and defect evolution in irradiated materials. Here we report that chemical disorder, with an increasing number of principal elements and/or altered concentrations of specific elements, in single-phase concentrated solid solution alloys can lead to substantial reduction in electron mean free path and orders of magnitude decrease in electrical and thermal conductivity. The subsequently slow energy dissipation affects defect dynamics at the early stages, and consequentially may result in less deleterious defects. Suppressed damage accumulation with increasing chemical disorder from pure nickel to binary and to more complex quaternary solid solutions is observed. Understanding and controlling energy dissipation and defect dynamics by altering alloy complexity may pave the way for new design principles of radiation-tolerant structural alloys for energy applications. PMID:26507943

  16. Influence of chemical disorder on energy dissipation and defect evolution in concentrated solid solution alloys.

    PubMed

    Zhang, Yanwen; Stocks, G Malcolm; Jin, Ke; Lu, Chenyang; Bei, Hongbin; Sales, Brian C; Wang, Lumin; Béland, Laurent K; Stoller, Roger E; Samolyuk, German D; Caro, Magdalena; Caro, Alfredo; Weber, William J

    2015-10-28

    A grand challenge in materials research is to understand complex electronic correlation and non-equilibrium atomic interactions, and how such intrinsic properties and dynamic processes affect energy transfer and defect evolution in irradiated materials. Here we report that chemical disorder, with an increasing number of principal elements and/or altered concentrations of specific elements, in single-phase concentrated solid solution alloys can lead to substantial reduction in electron mean free path and orders of magnitude decrease in electrical and thermal conductivity. The subsequently slow energy dissipation affects defect dynamics at the early stages, and consequentially may result in less deleterious defects. Suppressed damage accumulation with increasing chemical disorder from pure nickel to binary and to more complex quaternary solid solutions is observed. Understanding and controlling energy dissipation and defect dynamics by altering alloy complexity may pave the way for new design principles of radiation-tolerant structural alloys for energy applications.

  17. Development of Shape Memory Alloys- Challenges and Solutions

    NASA Technical Reports Server (NTRS)

    Benafan, Othmane

    2016-01-01

    Shape memory alloys (SMAs) are a unique class of multifunctional materials that have the ability to recover large deformations or generate high stresses in response to thermal, mechanical andor electromagnetic stimuli. These abilities have made them a viable option for actuation systems in aerospace, medical, and automotive applications, amongst others. However, despite many advantages and the fact that SMA actuators have been developed and used for many years, so far they have only found service in a limited range of applications. In order to expand their applications, further developments are needed to increase their reliability and stability and to address processing, testing and qualification needed for large-scale commercial application of SMA actuators. In this seminar, historical inhibitors of SMA applications and current research efforts by NASA Glenn Research Center and collaborators will be discussed. Relationships between fundamental physicalscientific understanding, and the direct transition to engineering and design of mechanisms using these novel materials will be highlighted. Examples will be presented related to targeted alloy development, microstructural control, and bulk-scale testing as a function of stresses, temperatures and harsh environments. The seminar will conclude with a summary of SMA applications under development and current advances.

  18. Behavior of Dental/Implant Alloys in Commercial Mouthwash Solution Studied by Electrochemical Techniques

    NASA Astrophysics Data System (ADS)

    Mareci, Daniel; Strugaru, Sorin Iacob; Iacoban, Sorin; Bolat, Georgiana; Munteanu, Corneliu

    2013-03-01

    This study investigates the electrochemical behavior of the various dental materials: Paliag (Ag-Pd based), Wiron 99 (Ni-Cr based), Cp-Ti (commercial pure titanium), and experimental Ti12Mo5Ta alloy in commercial mouthwash solution with 500 ppm F- (Oral B®) and compares it with the behavior of the same dental materials in artificial saliva. Linear potentiodynamic polarization (LPP) and electrochemical impedance spectroscopy (EIS) are the electrochemical procedures of investigation. The passivation of all dental samples in artificial saliva and mouthwash solution occurred spontaneously at open circuit potential. The corrosion current density of all tested dental materials in mouthwash solution were low (1-2 μA/cm2). The results suggest a non-predominant fluoride effect on the passive layer formed on all samples at open circuit potential. No passivation could be established with Paliag alloy when polarized in mouthwash solution. The EIS results confirm that all dental sample exhibit passivity in mouthwash solution at open circuit potential (polarization resistance was around 5 × 105 Ω cm2). For Paliag alloy after LPP in mouthwash solution the protectiveness passive layer was no more present. The corrosion resistances of four dental materials in mouthwash solution are in the following order: Ti12Mo5Ta > Cp-Ti > Wiron 99 > Paliag.

  19. Influence of dissolved organic matter and manganese oxides on metal speciation in soil solution: A modelling approach.

    PubMed

    Schneider, Arnaud R; Ponthieu, Marie; Cancès, Benjamin; Conreux, Alexandra; Morvan, Xavier; Gommeaux, Maxime; Marin, Béatrice; Benedetti, Marc F

    2016-06-01

    Trace element (TE) speciation modelling in soil solution is controlled by the assumptions made about the soil solution composition. To evaluate this influence, different assumptions using Visual MINTEQ were tested and compared to measurements of free TE concentrations. The soil column Donnan membrane technique (SC-DMT) was used to estimate the free TE (Cd, Cu, Ni, Pb and Zn) concentrations in six acidic soil solutions. A batch technique using DAX-8 resin was used to fractionate the dissolved organic matter (DOM) into four fractions: humic acids (HA), fulvic acids (FA), hydrophilic acids (Hy) and hydrophobic neutral organic matter (HON). To model TE speciation, particular attention was focused on the hydrous manganese oxides (HMO) and the Hy fraction, ligands not considered in most of the TE speciation modelling studies in soil solution. In this work, the model predictions of free ion activities agree with the experimental results. The knowledge of the FA fraction seems to be very useful, especially in the case of high DOM content, for more accurately representing experimental data. Finally, the role of the manganese oxides and of the Hy fraction on TE speciation was identified and, depending on the physicochemical conditions of the soil solution, should be considered in future studies.

  20. Study on Corrosion and Stress Corrosion Cracking Behaviors of AZ31 Alloy in Sodium Sulfate Solution

    NASA Astrophysics Data System (ADS)

    He, Xiuli; Yan, Zhifeng; Liang, Hongyu; Wei, Yinghui

    2017-05-01

    The potentiodynamic polarization test and slow strain rate tensile test were carried out in 3.5 wt.% Na2SO4 solution with different pH values (2, 7, and 12). It was found that the SCC susceptibility of AZ31 magnesium alloy in 3.5 wt.% Na2SO4 solution was deteriorated significantly with the decreasing pH. This was consistent with the electrochemical properties. There were filiform corrosion forms on the specimen surface after slow strain rate tensile test in 3.5 wt.% Na2SO4 solution, which indicated the characteristics of general corrosion. Moreover, there were multiple stress corrosion crack initiation sources. The SCC fracture of AZ31 magnesium alloy in air was a mix type, while it was cleavage fracture in 3.5 wt.% Na2SO4 solution.

  1. Twin solution calorimeter determines heats of formation of alloys at high temperatures

    NASA Technical Reports Server (NTRS)

    Darby, J. B., Jr.; Kleb, R.; Kleppa, O. J.

    1968-01-01

    Calvert-type, twin liquid metal solution calorimeter determines the heats of formation of transition metal alloys at high temperatures. The twin differential calorimeter measures the small heat effects generated over extended periods of time, has maximum operating temperature of 1073 degrees K and an automatic data recording system.

  2. Ion release and surface oxide composition of AISI 316L, Co-28Cr-6Mo, and Ti-6Al-4V alloys immersed in human serum albumin solutions.

    PubMed

    Karimi, Shima; Alfantazi, Akram M

    2014-07-01

    The long-term weight loss, ion release, and surface composition of 316L, Co-28Cr-6Mo and Ti-6Al-4V alloys were investigated in a simulated body environment. The samples were immersed in phosphate-buffered saline (PBS) solutions with various human serum albumin (HSA) concentrations for 8, 14, and 22 weeks. The specimens initially lost weight up to 14 weeks and then slightly gained weight. The analysis of the released ions was performed by induced coupled plasma-optical emission spectrometer (ICP-OES). The results revealed that the precipitation of the dissolved Fe and Co could cause the weight gain of the 316L and Co-28Cr-6Mo alloys. The surface chemistry of the specimens was determined by X-ray photoelectron spectroscopy (XPS). The XPS analysis of Co-28Cr-6Mo alloy showed that the interaction of Mo with HSA is different from Mo with bovine serum albumin (BSA). This was also observed for Na adsorption into the oxide layer of Ti-6Al-4V alloy in the presence of HSA and BSA.

  3. The configurational entropy of mixing of metastable random solid solution in complex multicomponent alloys

    NASA Astrophysics Data System (ADS)

    He, Q. F.; Ye, Y. F.; Yang, Y.

    2016-10-01

    Since the advent of "high-entropy" alloys, the simple ideal mixing rule has been commonly used to calculate the configurational entropy of mixing for these multicomponent alloys. However, there have been increasing experimental evidence reported recently showing that the ideal mixing rule tends to overestimate the configurational entropy of mixing in the multicomponent alloys, particularly at a low temperature. In contrast to the ideal mixing rule, here we provide a formula to assess the configurational entropy of mixing in random solid-solution multicomponent alloys by considering the possible correlations among the constituent elements due to various factors, such as atomic size misfit and chemic bond misfit, which may disturb the potential energy of the system and thus reduce the configurational entropy of mixing. With our entropy formulation, the correlation is explored between the configuration entropy of mixing of different alloys and the general character of the phases formed, such as single- or multiple-phased crystalline phase versus amorphous phase. Being in good agreement with the simulation and experimental results, our work provides an analytical framework that could be further used to explore phase stability in complex multicomponent alloys.

  4. Hydrogen assisted cracking and inhibition of spring alloys in acidizing solutions

    SciTech Connect

    Coyle, W.R.; Chitwood, G.B.; Rice, P.W.; Walker, M.L.

    1994-12-31

    Several experiments were conducted to investigate and compare the hydrogen assisted cracking resistance of high strength, corrosion resistant spring alloys to acidizing fluids. Two cobalt-based alloys, UNS R30035 and UNS R30003, and one nickel-based alloy, UNS N07750, were evaluated. The tests involved exposing stressed spring segments of all alloys and C-rings of R30035 to uninhibited 28% HCl, 28% HCl with two different inhibitors, and the NACE TM0177 solution. Failures of N07750 spring segments in the uninhibited acid parallel field performance of this alloy. There were no failures of the R30035 or R30003 spring segments in the environments tested. Springs made from N07750 are more susceptible to hydrogen embrittlement than either R30035 or R30003. The C-ring tests of R30035 revealed the benefit of corrosion inhibition as a means of elevating the threshold cracking stress and increasing the time to failure in corrosive media. A strong beneficial effect of elevated-temperature thermal processing was observed for UNS R30035. High performance acidizing inhibitors are required in order to provide effective protection to high alloy spring materials.

  5. Effects of solute elements on irradiation hardening and microstructural evolution in low alloy steels

    NASA Astrophysics Data System (ADS)

    Fujii, Katsuhiko; Ohkubo, Tadakatsu; Fukuya, Koji

    2011-10-01

    The effects of the elements Mn, Ni, Si and Cu on irradiation hardening and microstructural evolution in low alloy steels were investigated in ion irradiation experiments using five kinds of alloys prepared by removing Mn, Ni and Si from, and adding 0.05 wt.%Cu to, the base alloy (Fe-1.5Mn-0.5Ni-0.25Si). The alloy without Mn showed less hardening and the alloys without Ni or Si showed more hardening. The addition of Cu had hardly any influence on hardening. These facts indicated that Mn enhanced hardening and that Ni and Si had some synergetic effects. The formation of solute clusters was not confirmed by atom probe (AP) analysis, whereas small dislocation loops were identified by TEM observation. The difference in hardening between the alloys with and without Mn was qualitatively consistent with loop formation. However, microstructural components that were not detected by the AP and TEM were assumed to explain the hardening level quantitatively.

  6. Effect of C content on the mechanical properties of solution treated as-cast ASTM F-75 alloys.

    PubMed

    Herrera, M; Espinoza, A; Méndez, J; Castro, M; López, J; Rendón, J

    2005-07-01

    The mechanical properties of solution treated ASTM F-75 alloys with various carbon contents have been studied. Alloys cast under the same conditions were subjected to solution treatment for several periods and then their tensile properties were evaluated. In the as-cast conditions, the alloys exhibited higher strength values with increasing carbon content whereas their ductility was not significantly affected. For the solution treated alloys, the variation of the strength was characterized by a progressive increase for short treatment times until a maximum value was achieved, which was followed by a diminution in this property for longer treatment times. This behavior was more accentuated for the case of the alloys with medium carbon contents, which also exhibited the highest values of strength. Furthermore, the alloy's ductility was enhanced progressively with increasing solution treatment time. This improvement in ductility was significantly higher for the medium carbon alloys compared with the rest of the studied alloys. Thus, high and low carbon contents in solution treated ASTM F-75 alloys did not produced sufficiently high tensile properties.

  7. Poly(N-vinylimidazole) gels as insoluble buffers that neutralize acid solutions without dissolving.

    PubMed

    Horta, Arturo; Piérola, Inés F

    2009-04-02

    Typical buffers are solutions containing weak acids or bases. If these groups were anchored to insoluble gels, what would be their behavior? Simple thermodynamics is used to calculate the pH in two-phase systems that contain the weak acid or base fixed to only one of the phases and is absent in the other. The experimental reference of such systems are pH sensitive hydrogels and heterogeneous systems of biological interest. It is predicted that a basic hydrogel immersed in slightly acidic solutions should absorb the acid and leave the external solution exactly neutral (pH 7). This is in accordance with experimental results of cross-linked poly(N-vinylimidazole). The pH 7 cannot be obtained if the system were homogeneous; the confinement of the weak base inside the gel phase is a requisite for this neutral pH in the external solution. The solution inside the gel is regulated to a much higher pH, which has important implications in studies on chemical reactions and physical processes taking place inside a phase insoluble but in contact with a solution.

  8. Phase Stability under Irradiation of Precipitates and Solid Solutions in Model ALloys and in ODS Alloys Relevant for Gen IV

    SciTech Connect

    Arthur T. Motta; Robert C. Birtcher

    2007-10-17

    The overall objective of this program is to investigate the irradiation-altered phase stability of oxide precipitates in ODS steels and of model alloy solid solutions of associated systems. This information can be used to determine whether the favorable mechanical propertiies of these steels are maintained under irradiation, thus addressing one of the main materials research issues for this class of steels as identified by the GenIV working groups. The research program will also create fundamental understanding of the irradiation precipitation/dissolution problem by studying a "model" system in which the variables can be controlled and their effects understood individually.

  9. Influence of Dy in solid solution on the degradation behavior of binary Mg-Dy alloys in cell culture medium.

    PubMed

    Yang, Lei; Ma, Liangong; Huang, Yuanding; Feyerabend, Frank; Blawert, Carsten; Höche, Daniel; Willumeit-Römer, Regine; Zhang, Erlin; Kainer, Karl Ulrich; Hort, Norbert

    2017-06-01

    Rare earth element Dy is one of the promising alloying elements for magnesium alloy as biodegradable implants. To understand the effect of Dy in solid solution on the degradation of Mg-Dy alloys in simulated physiological conditions, the present work studied the microstructure and degradation behavior of Mg-Dy alloys in cell culture medium. It is found the corrosion resistance enhances with the increase of Dy content in solid solution in Mg. This can be attributed to the formation of a relatively more corrosion resistant Dy-enriched film which decreases the anodic dissolution of Mg. Copyright © 2017 Elsevier B.V. All rights reserved.

  10. Development Of ABEC Column For Separation Of Tc-99 From Northstar Dissolved Target Solution

    SciTech Connect

    Stepinski, Dominique C.; Bennett, Megan E.; Naik, Seema R.; ling, lei; Wang, N-H. Linda; Vandegrift, George F.

    2016-12-01

    Batch and column breakthrough experiments were performed to determine isotherms and mass-transfer parameters for adsorption of Tc on aqueous biphasic extraction chromatographic (ABEC) sorbent in two solutions: 200 g/L Mo, 5.1 M K+, 1 M OH-, and 0.1 M NO3- (Solution A) and 200 g/L Mo, 9.3 M K+, 5 M OH-, and 0.1 M NO3- (Solution B). Good agreement was found between the isotherm values obtained by batch and column breakthrough studies for both Solutions A and B. Potassium-pertechnetate intra-particle diffusivity on ABEC resin was estimated by VERSE simulations, and good agreement was found among a series of column-breakthrough experiments at varying flow velocities, column sizes, and technetium concentrations. However, testing of 10 cc cartridges provided by NorthStar with Solutions A and B did not give satisfactory results, as significant Tc breakthrough was observed and ABEC cartridge performance varied widely among experiments. These different experimental results are believed to be due to inconsistent preparation of the ABEC resin prior to packing and/or inconsistent packing.

  11. Effect of Cu content on exfoliation corrosion and electrochemical corrosion of A7N01 aluminum alloy in EXCO solution

    NASA Astrophysics Data System (ADS)

    He, Yaling; Wang, Xiaomin; Hu, Jie; Zhou, Qiang; Chen, Hui

    2017-07-01

    The exfoliation corrosion (EXCO) sensitivities and electrochemical corrosions of A7N01 aluminum (Al) alloys with 0.074% and 0.136% Cu contents were investigated in EXCO solution. The exfoliation corrosion developed more rapidly for the alloy with 0.136% Cu by expressing higher exfoliation rate and deeper corrosion pits as observed by SEM and laser confocal scanning microscopy (LCSM). In EXCO solution, the alloy with 0.136% Cu content showed lower open-circuit potential (OCP) than the alloy with 0.074% Cu content. The alloy with 0.136% Cu content had bigger “hysteresis loop” in cyclic polarization curve which meant lower self-passivation ability. In electrochemical impedance spectroscopy plot, its curvature radius and capacitance index were lower. The electrochemical test results revealed that the alloy with 0.136% Cu content showed more severe electrochemical corrosion than the alloy with 0.074% Cu content, consistent with the exfoliation corrosion results. The microstructures of two alloys were observed through optical microscopy (OM) and transmission electron microscopy (TEM). The continuous distribution of the equilibrium precipitate η-MgZn2 on grain boundaries, the decreasing of the width of precipitate-free zone (PFZ) and the coarse Cu-Fe-Si-rich phase were responsible for the higher corrosion sensitivity of the Al alloy with 0.136% Cu than that of Al alloy with 0.074% Cu content in EXCO solution.

  12. Corrosion behavior of niobium and Nb-25 wt% Ta alloy in sulfuric acid solutions

    SciTech Connect

    Robin, A.; Nunes, C.A. ); de Almeida, M.E. )

    1991-06-01

    In this paper the corrosion behavior of niobium and Nb-25 wt% Ta alloy in H{sub 2} SO{sub 4} solutions has been studied. Using mass-loss techniques, the influences of H{sub 2}SO{sub 4} concentration, temperature, and exposure time have been examined. The Nb-Ta alloy is more corrosion resistant than pure niobium. The obtained corrosion data allowed the construction of iso-corrosion curves of both materials in sulfuric acid below and above the boiling point.

  13. Magnesium Alloys in U.S. Military Applications: Past, Current and Future Solutions

    NASA Astrophysics Data System (ADS)

    Mathaudhu, Suveen N.; Nyberg, Eric A.

    Since the 1940's Mg-alloys have been used for military applications, from aircraft components to ground vehicles. The drive for usage was primarily availability and lightweighting of military systems. But the promise of widespread military usage was not met largely based on corrosion and flammability concerns, poor mechanical behavior and inferior ballistic response. This review paper will cover historical, current and potential future applications with a focus on scientific, engineering and social barriers relevant to integration of Mg-alloy. It will also present mechanical and physical property improvements solutions which are currently being developed to address these issues.

  14. MAGNESIUM ALLOYS IN US MILITARY APPLICATIONS: PAST, CURRENT AND FUTURE SOLUTIONS

    SciTech Connect

    Mathaudhu, Suveen N.; Nyberg, Eric A.

    2010-02-26

    Since the 1940’s Mg-alloys have been used for military applications, from aircraft components to ground vehicles. The drive for usage was primarily availability and lightweighting of military systems. But the promise of widespread military usage was not met largely based on corrosion and flammability concerns, poor mechanical behavior and inferior ballistic response. This review paper will cover historical, current and potential future applications with a focus on scientific, engineering and social barriers relevant to integration of Mg-alloy. It will also present mechanical and physical property improvements solutions which are currently being developed to address these issues.

  15. Solid-Solution Alloying of Immiscible Ru and Cu with Enhanced CO Oxidation Activity.

    PubMed

    Huang, Bo; Kobayashi, Hirokazu; Yamamoto, Tomokazu; Matsumura, Syo; Nishida, Yoshihide; Sato, Katsutoshi; Nagaoka, Katsutoshi; Kawaguchi, Shogo; Kubota, Yoshiki; Kitagawa, Hiroshi

    2017-03-24

    We report on novel solid-solution alloy nanoparticles (NPs) of Ru and Cu that are completely immiscible even above melting point in bulk phase. Powder X-ray diffraction, scanning transmission electron microscopy, and energy-dispersive X-ray measurements demonstrated that Ru and Cu atoms were homogeneously distributed in the alloy NPs. Ru0.5Cu0.5 NPs demonstrated higher CO oxidation activity than fcc-Ru NPs, which are known as one of the best monometallic CO oxidation catalysts.

  16. Conformational arrangement of dissolved humic substances. Influence of solution composition on association of humic molecules

    SciTech Connect

    Conte, P.; Piccolo, A.

    1999-05-15

    The characteristics and quantity of humic substances greatly affects the environmental fate of organic pollutants in soils and natural waters. The authors studied the conformational changes of humic and fulvic acids of different chemical nature by high-pressure size-exclusion chromatography (HPSEC) after dissolution in mobile phases differing in composition but constant in ionic strength. Modification of a neutral mobile phase by addition of methanol, hydrochloric acid, and acetic acid produced, in the order, a progressive decrease in molecular size. Size diminishing was shown by increasingly larger elution volumes at a refractive index detector and by concomitant reductions of peaks absorbance at a UV-vis detector. The decrease of molecular absorptivity (the phenomenon of hypochromism) proved that size reduction of dissolved humic substances was due more to disruption of an only apparent high-molecular-size arrangement into several smaller molecular associations than to coiling down of a macromolecular structure. The most significant conformational changes occurred in acidic mobile phases where hydrogen bondings formation was induced, suggesting that the large and easily disruptable humic conformation was held together predominantly by weak hydrophobic forces.

  17. Thermal Stability of Nanocrystalline Alloys by Solute Additions and A Thermodynamic Modeling

    NASA Astrophysics Data System (ADS)

    Saber, Mostafa

    Nanocrystalline alloys show superior properties due to their exceptional microstructure. Thermal stability of these materials is a critical aspect. It is well known that grain boundaries in nanocrystalline microstructures cause a significant increase in the total free energy of the system. A driving force provided to reduce this excess free energy can cause grain growth. The presence of a solute addition within a nanocrystalline alloy can lead to the thermal stability. Kinetic and thermodynamic stabilization are the two basic mechanisms with which stability of a nanoscale grain size can be achieved at high temperatures. The basis of this thesis is to study the effect of solute addition on thermal stability of nanocrystalline alloys. The objective is to determine the effect of Zr addition on the thermal stability of mechanically alloyed nanocrysatillne Fe-Cr and Fe-Ni alloys. In Fe-Cr-Zr alloy system, nanoscale grain size stabilization was maintained up to 900 °C by adding 2 at% Zr. Kinetic pinning by intermetallic particles in the nanoscale range was identified as a primary mechanism of thermal stabilization. In addition to the grain size strengthening, intermetallic particles also contribute to strengthening mechanisms. The analysis of microhardness, XRD data, and measured grain sizes from TEM micrographs suggested that both thermodynamic and kinetic mechanisms are possible mechanisms. It was found that alpha → gamma phase transformation in Fe-Cr-Zr system does not influence the grain size stabilization. In the Fe-Ni-Zr alloy system, it was shown that the grain growth in Fe-8Ni-1Zr alloy is much less than that of pure Fe and Fe-8Ni alloy at elevated temperatures. The microstructure of the ternary Fe-8Ni-1Zr alloy remains in the nanoscale range up to 700 °C. Using an in-situ TEM study, it was determined that drastic grain growth occurs when the alpha → gamma phase transformation occurs. Accordingly, there can be a synergistic relationship between grain growth

  18. Effect of Solute Diffusion on Dendrite Growth in the Molten Pool of Al-Cu Alloy

    NASA Astrophysics Data System (ADS)

    Zhan, Xiaohong; Gu, Cheng; Liu, Yun; Wei, Yanhong

    2017-10-01

    A cellular automaton (CA)-finite difference model is developed to simulate dendrite growth and solute diffusion during solidification process in the molten pool of Al-Cu alloy. In order to explain the interaction between the dendritic growth and solute distribution, a series of CA simulations with different solute diffusion velocity coefficients are carried out. It is concluded that the solute concentration increases with dendrite growing and solute accumulation in the dendrite tip. Converged value of the dendrite tip growth velocity is about 480 μm/s if the mesh size is refined to 2 μm or less. Growth of the primary dendrite and the secondary dendrite is mainly influenced by solute diffusion at the dendrite tips. And growth of secondary and tertiary dendrites is mainly influenced by solute diffusion at interdendrite.

  19. Effect of dissolved organic matter source and character on microbial Hg methylation in Hg–S–DOM solutions

    USGS Publications Warehouse

    Graham, Andrew M.; Aiken, George R.; Gilmour, Cynthia

    2013-01-01

    Dissolved organic matter (DOM) is a key component of fate and transport models for most metals, including mercury (Hg). Utilizing a suite of diverse DOM isolates, we demonstrated that DOM character, in addition to concentration, influences inorganic Hg (Hg(II)i) bioavailability to Hg-methylating bacteria. Using a model Hg-methylating bacterium, Desulfovibrio desulfuricansND132, we evaluated Hg-DOM-sulfide bioavailability in washed-cell assays at environmentally relevant Hg/DOM ratios (∼1–8 ng Hg/mg C) and sulfide concentrations (1–1000 μM). All tested DOM isolates significantly enhanced Hg methylation above DOM-free controls (from ∼2 to >20-fold for 20 mg C/L DOM solutions), but high molecular weight/highly aromatic DOM isolates and/or those with high sulfur content were particularly effective at enhancing Hg methylation. Because these experiments were conducted under conditions of predicted supersaturation with respect to metacinnabar (β-HgS(s)), we attribute the DOM-dependent enhancement of Hg(II)i bioavailability to steric and specific chemical (e.g., DOM thiols) inhibition of β-HgS(s) growth and aggregation by DOM. Experiments examining the role of DOM across a wide sulfide gradient revealed that DOM only enhances Hg methylation under fairly low sulfide conditions (≲30 μM), conditions that favor HgS nanoparticle/cluster formation relative to dissolved HgS species.

  20. Factors affecting total dissolved solids concentration of γ-ray-irradiated aqueous hexamethylenetetramine solution: a dosimetric study.

    PubMed

    Sife-Eldeen, Kh A

    2014-12-01

    A new γ-ray-radiation dosimetric system (TDS-HMTA), comprising a 'total dissolved solids (TDS)' meter and 0.02 M aqueous hexamethylenetetramine (HMTA) solution, is introduced for medical and biological applications. Gamma-ray radiolysis of aqueous HTMA solutions increases the concentrations (ppm) of TDS, which is measured by the TDS meter. The effects of HMTA concentration, absorbed radiation dose, absorbed dose rate, and storage time on the TDS concentration of irradiated HMTA solutions were studied. It was found that 0.02 M aqueous HMTA solution yields the highest sensitivity to γ-ray-radiation according to TDS concentration measurements. The effect of absorbed radiation dose was studied in the range 1.64-435.5 kGy. The TDS concentration increases linearly up to the maximum of the studied absorbed radiation dose range (R(2) = 0.9965). The overall coefficient of variation (CV %) associated with TDS concentration measurements of 0.02 M HMTA solution as a function of absorbed dose was found to be 0.732%. The effect of dose rate on the TDS concentration was studied in the range 0.33-3.31 kGy/h. It was found, also, that the TDS concentration is relatively stable over a storage period of 144 h after irradiation with different doses. The tissue equivalency of 0.02 M aqueous HMTA solutions allow it to be used for radiation dose measurement during sterilization in human tissue banks. Therefore, this system (TDS-HMTA) could be considered as a promising candidate for γ-ray radiation dosimetry in technical, medical and research fields.

  1. Analytical solutions to dissolved contaminant plume evolution with source depletion during carbon dioxide storage

    NASA Astrophysics Data System (ADS)

    Yang, Yong; Liu, Yongzhong; Yu, Bo; Ding, Tian

    2016-06-01

    Volatile contaminants may migrate with carbon dioxide (CO2) injection or leakage in subsurface formations, which leads to the risk of the CO2 storage and the ecological environment. This study aims to develop an analytical model that could predict the contaminant migration process induced by CO2 storage. The analytical model with two moving boundaries is obtained through the simplification of the fully coupled model for the CO2-aqueous phase -stagnant phase displacement system. The analytical solutions are confirmed and assessed through the comparison with the numerical simulations of the fully coupled model. Then, some key variables in the analytical solutions, including the critical time, the locations of the dual moving boundaries and the advance velocity, are discussed to present the characteristics of contaminant migration in the multi-phase displacement system. The results show that these key variables are determined by four dimensionless numbers, Pe, RD, Sh and RF, which represent the effects of the convection, the dispersion, the interphase mass transfer and the retention factor of contaminant, respectively. The proposed analytical solutions could be used for tracking the migration of the injected CO2 and the contaminants in subsurface formations, and also provide an analytical tool for other solute transport in multi-phase displacement system.

  2. Analytical solutions to dissolved contaminant plume evolution with source depletion during carbon dioxide storage.

    PubMed

    Yang, Yong; Liu, Yongzhong; Yu, Bo; Ding, Tian

    2016-06-01

    Volatile contaminants may migrate with carbon dioxide (CO2) injection or leakage in subsurface formations, which leads to the risk of the CO2 storage and the ecological environment. This study aims to develop an analytical model that could predict the contaminant migration process induced by CO2 storage. The analytical model with two moving boundaries is obtained through the simplification of the fully coupled model for the CO2-aqueous phase -stagnant phase displacement system. The analytical solutions are confirmed and assessed through the comparison with the numerical simulations of the fully coupled model. Then, some key variables in the analytical solutions, including the critical time, the locations of the dual moving boundaries and the advance velocity, are discussed to present the characteristics of contaminant migration in the multi-phase displacement system. The results show that these key variables are determined by four dimensionless numbers, Pe, RD, Sh and RF, which represent the effects of the convection, the dispersion, the interphase mass transfer and the retention factor of contaminant, respectively. The proposed analytical solutions could be used for tracking the migration of the injected CO2 and the contaminants in subsurface formations, and also provide an analytical tool for other solute transport in multi-phase displacement system. Copyright © 2016 Elsevier B.V. All rights reserved.

  3. Multi-component solid solution alloys having high mixing entropy

    DOEpatents

    Bei, Hongbin

    2015-10-06

    A multi-component high-entropy alloy includes a composition selected from the following group: VNbTaTiMoWRe, VNbTaTiMoW, VNbTaTiMoRe, VNbTaTiWRe, VNbTaMoWRe, VNbTiMoWRe, VTaTiMoWRe, NbTaTiMoWRe, VNbTaTiMo, VNbTaTiW, VNbTaMoW, VNbTiMoW, VTaTiMoW, NbTaTiMoW, VNbTaTiRe, VNbTaMoRe, VNbTiMoRe, VTaTiMoRe, NbTaTiMoRe, VNbTaWRe, VNbTiWRe, VTaTiWRe, NbTaTiWRe, VNbMoWRe, VTaMoWRe, NbTaMoWRe, VTiMoWRe, NbTiMoWRe, TaTiMoWRe, wherein relative amounts of each element vary by no more than .+-.15 atomic %.

  4. Alloy 22 Localized Corrosion Susceptibility In Aqueous Solutions Of Chloride And Nitrate Salts Of Sodium And Potassium At 110 - 150?C

    SciTech Connect

    Felker, S; Hailey, P D; Lian, T; Staggs, K J; Gdowski, G E

    2006-01-17

    Alloy 22 (a nickel-chromium-molybdenum-tungsten alloy) is being investigated for use as the outer barrier of waste containers for a high-level nuclear waste repository in the thick unsaturated zone at Yucca Mountain, Nevada. Experiments were conducted to assess crevice corrosion of Alloy 22 in de-aerated aqueous solutions of chloride and nitrate salts of potassium and sodium in the temperature range 110-150 C (some limited testing was also conducted at 90 C). Electrochemical tests were run in neutral salt solutions without acid addition and others were run in salt solutions with an initial hydrogen ion concentration of 10{sup -4} molal. The Alloy 22 specimens were weld prism specimens and de-aeration was performed with nitrogen gas. No evidence of crevice corrosion was observed in the range 125-150 C. In the 120 to 160 C temperature range, the anionic concentration of stable aqueous solutions is dominated by nitrate relative to chloride. At nominally 120 C, the minimum nitrate to chloride ratio is about 4.5, and it increases to about 22 at nominally 155 C. The absence of localized corrosion susceptibility in these solutions is attributed to the known inhibiting effect of the nitrate anion. At 110 C, aqueous solutions can have dissolved chloride in excess of nitrate. Localized corrosion was observed at nitrate to chloride ratios up to 1.0, the highest ratio tested. The extent of localized corrosion was confined to the crevice region of the samples, and was limited for nitrate to chloride ratios greater than or equal to 0.3. Aqueous solution chemistry studies indicate that nitrate to chloride ratios of less than 0.5 are possible for temperatures up to nominally 116 C. However, the exact upper temperature limit is unknown and no electrochemical testing was done at these temperatures. Limited comparison between 8 m Cl aqueous solutions of Na + K on the one hand and Ca on the other indicated similar electrochemical E{sub crit} values and similar morphology of attack

  5. Green and Facile Synthesis of Pd-Pt Alloy Nanoparticles by Laser Irradiation of Aqueous Solution.

    PubMed

    Nakamura, Takahiro; Sato, Shunichi

    2015-01-01

    Solid-solution palladium-platinum (Pd-Pt) alloy nanoparticles (NPs) with fully tunable compositions were directly fabricated through high-intensity laser irradiation of an aqueous solution of palladium and platinum ions without using any reducing agents or thermal processes. Transmission electron microscopy (TEM) observations showed that nanometer-sized particles were fabricated by laser irradiation of mixed aqueous solutions of palladium and platinum ions with different feeding ratios. The crystalline nature of the NPs was precisely characterized by X-ray diffraction (XRD). Despite the fact that, for the bulk systems, a pair of XRD peak was detected between the palladium and platinum peaks because of the large miscibility gap in the Pd-Pt binary phase diagram, only a single XRD peak was seen for the Pd-Pt NPs fabricated in the present study. Moreover, the peak position shifted from that of pure palladium towards platinum with increasing fraction of platinum ions in solution. Consequently, the interplanar spacings of the alloy NPs agreed well with the estimated values obtained from Vegard's law. These observations strongly indicate the formation of solid-solution Pd-Pt alloy NPs with fully tunable compositions. This technique is not only a "green" (environmentally-friendly) and facile process, but is also widely applicable to other binary and ternary systems.

  6. Generation of Hydroxyl Radicals from Dissolved Transition Metals in Surrogate Lung Fluid Solutions

    PubMed Central

    Vidrio, Edgar; Jung, Heejung; Anastasio, Cort

    2008-01-01

    Epidemiological research has linked exposure to atmospheric particulate matter (PM) to several adverse health effects, including cardiovascular and pulmonary morbidity and mortality. Despite these links, the mechanisms by which PM causes adverse health effects are poorly understood. The generation of hydroxyl radical (·OH) and other reactive oxygen species (ROS) through transition metal-mediated pathways is one of the main hypotheses for PM toxicity. In order to better understand the ability of particulate transition metals to produce ROS, we have quantified the amounts of ·OH produced from dissolved iron and copper in a cell-free, surrogate lung fluid (SLF). We also examined how two important biological molecules, citrate and ascorbate, affect the generation of ·OH by these metals. We have found that Fe(II) and Fe(III) produce little ·OH in the absence of ascorbate and citrate, but that they efficiently make ·OH in the presence of ascorbate and this is further enhanced when citrate is also added. In the presence of ascorbate, with or without citrate, the oxidation state of iron makes little difference on the amount of ·OH formed after 24 hours. In the case of Cu(II), the production of ·OH is greatly enhanced in the presence of ascorbate, but is inhibited by the addition of citrate. The mechanism for this effect is unclear, but appears to involve formation of a citrate-copper complex that is apparently less reactive than free, aquated copper in either the generation of HOOH or in the Fenton-like reaction of copper with HOOH to make ·OH. By quantifying the amount of ·OH that Fe and Cu can produce in surrogate lung fluid, we have provided a first step into being able to predict the amounts of ·OH that can be produced in the human lung from exposure to PM containing known amounts of transition metals. PMID:19148304

  7. Generation of Hydroxyl Radicals from Dissolved Transition Metals in Surrogate Lung Fluid Solutions.

    PubMed

    Vidrio, Edgar; Jung, Heejung; Anastasio, Cort

    2008-01-01

    Epidemiological research has linked exposure to atmospheric particulate matter (PM) to several adverse health effects, including cardiovascular and pulmonary morbidity and mortality. Despite these links, the mechanisms by which PM causes adverse health effects are poorly understood. The generation of hydroxyl radical (.OH) and other reactive oxygen species (ROS) through transition metal-mediated pathways is one of the main hypotheses for PM toxicity. In order to better understand the ability of particulate transition metals to produce ROS, we have quantified the amounts of .OH produced from dissolved iron and copper in a cell-free, surrogate lung fluid (SLF). We also examined how two important biological molecules, citrate and ascorbate, affect the generation of .OH by these metals. We have found that Fe(II) and Fe(III) produce little .OH in the absence of ascorbate and citrate, but that they efficiently make .OH in the presence of ascorbate and this is further enhanced when citrate is also added. In the presence of ascorbate, with or without citrate, the oxidation state of iron makes little difference on the amount of .OH formed after 24 hours. In the case of Cu(II), the production of .OH is greatly enhanced in the presence of ascorbate, but is inhibited by the addition of citrate. The mechanism for this effect is unclear, but appears to involve formation of a citrate-copper complex that is apparently less reactive than free, aquated copper in either the generation of HOOH or in the Fenton-like reaction of copper with HOOH to make .OH. By quantifying the amount of .OH that Fe and Cu can produce in surrogate lung fluid, we have provided a first step into being able to predict the amounts of .OH that can be produced in the human lung from exposure to PM containing known amounts of transition metals.

  8. In vitro corrosion behaviour of Ti-Nb-Sn shape memory alloys in Ringer's physiological solution.

    PubMed

    Rosalbino, F; Macciò, D; Scavino, G; Saccone, A

    2012-04-01

    The nearly equiatomic Ni-Ti alloy (Nitinol) has been widely employed in the medical and dental fields owing to its shape memory or superelastic properties. The main concern about the use of this alloy derives form the fact that it contains a large amount of nickel (55% by mass), which is suspected responsible for allergic, toxic and carcinogenic reactions. In this work, the in vitro corrosion behavior of two Ti-Nb-Sn shape memory alloys, Ti-16Nb-5Sn and Ti-18Nb-4Sn (mass%) has been investigated and compared with that of Nitinol. The in vitro corrosion resistance was assessed in naturally aerated Ringer's physiological solution at 37°C by corrosion potential and electrochemical impedance spectroscopy (EIS) measurements as a function of exposure time, and potentiodynamic polarization curves. Corrosion potential values indicated that both Ni-Ti and Ti-Nb-Sn alloys undergo spontaneous passivation due to spontaneously formed oxide film passivating the metallic surface, in the aggressive environment. It also indicated that the tendency for the formation of a spontaneous oxide is greater for the Ti-18Nb-5Sn alloy. Significantly low anodic current density values were obtained from the polarization curves, indicating a typical passive behaviour for all investigated alloys, but Nitinol exhibited breakdown of passivity at potentials above approximately 450 mV(SCE), suggesting lower corrosion protection characteristics of its oxide film compared to the Ti-Nb-Sn alloys. EIS studies showed high impedance values for all samples, increasing with exposure time, indicating an improvement in corrosion resistance of the spontaneous oxide film. The obtained EIS spectra were analyzed using an equivalent electrical circuit representing a duplex structure oxide film, composed by an outer and porous layer (low resistance), and an inner barrier layer (high resistance) mainly responsible for the alloys corrosion resistance. The resistance of passive film present on the metals' surface

  9. Thermophysical properties of Ni-containing single-phase concentrated solid solution alloys

    SciTech Connect

    Jin, Ke; Mu, Sai; An, Ke; Porter, Wallace D.; Samolyuk, German D.; Stocks, George Malcolm; Bei, Hongbin

    2016-12-27

    For this research temperature dependent thermophysical properties, including specific heat capacity, lattice thermal expansion, thermal diffusivity and conductivity, have been systematically studied in Ni and eight Ni-containing single-phase face-centered-cubic concentrated solid solution alloys, at elevated temperatures up to 1273 K. The alloys have similar specific heat values of 0.4–0.5 J·g-1·K-1 at room temperature, but their temperature dependence varies greatly due to Curie and K-state transitions. The lattice, electronic, and magnetic contributions to the specific heat have been separated based on first-principles methods in NiCo, NiFe, Ni-20Cr and NiCoFeCr. The alloys have similar thermal expansion behavior, with the exception that NiFe and NiCoFe have much lower thermal expansion coefficient in their ferromagnetic state due to magnetostriction effects. Calculations based on the quasi-harmonic approximation accurately predict the temperature dependent lattice parameter of NiCo and NiFe with < 0.2% error, but underestimated that of Ni-20Cr by 1%, compared to the values determined from neutron diffraction. In addition, all the alloys containing Cr have very similar thermal conductivity, which is much lower than that of Ni and the alloys without Cr, due to the large magnetic disorder.

  10. Thermophysical properties of Ni-containing single-phase concentrated solid solution alloys

    DOE PAGES

    Jin, Ke; Mu, Sai; An, Ke; ...

    2016-12-27

    For this research temperature dependent thermophysical properties, including specific heat capacity, lattice thermal expansion, thermal diffusivity and conductivity, have been systematically studied in Ni and eight Ni-containing single-phase face-centered-cubic concentrated solid solution alloys, at elevated temperatures up to 1273 K. The alloys have similar specific heat values of 0.4–0.5 J·g-1·K-1 at room temperature, but their temperature dependence varies greatly due to Curie and K-state transitions. The lattice, electronic, and magnetic contributions to the specific heat have been separated based on first-principles methods in NiCo, NiFe, Ni-20Cr and NiCoFeCr. The alloys have similar thermal expansion behavior, with the exception that NiFemore » and NiCoFe have much lower thermal expansion coefficient in their ferromagnetic state due to magnetostriction effects. Calculations based on the quasi-harmonic approximation accurately predict the temperature dependent lattice parameter of NiCo and NiFe with < 0.2% error, but underestimated that of Ni-20Cr by 1%, compared to the values determined from neutron diffraction. In addition, all the alloys containing Cr have very similar thermal conductivity, which is much lower than that of Ni and the alloys without Cr, due to the large magnetic disorder.« less

  11. Hydrogen generation using the corrosion of Al-Sn and Al-Si alloys in an alkaline solution

    NASA Astrophysics Data System (ADS)

    Yoo, Jeong-Hyun; Yun, Kwi-Sub; Kalubarme, Ramchandra S.; Park, Choong-Nyeon; Park, Chan-Jin

    2014-07-01

    We investigated the effects of adding Sn and Si to Al alloys on the corrosion of the alloys and the generation of hydrogen from an alkaline solution using the alloys. With increasing Sn content of up to 20 wt% in the Al-Sn alloy, the volume fraction of the Sn phase as a cathodic site at grain boundaries increased, and consequently, the hydrogen generation rate from an alkaline solution by the alloy also increased. In addition, the quenched Al-Sn alloys had smaller grain sizes compared to the furnace-cooled alloys, and accordingly, exhibited a slightly higher hydrogen generation rate. A galvanic cell was formed between the Al grain and the Sn phase of the grain boundary, and accordingly, intergranular type corrosion was observed on the Al-Sn alloys. Compared with the Al-Sn alloys, a more uniform type corrosion was observed on the Al-Si alloys because the nobler Si was uniformly distributed in the eutectic region formed between the primary Al grains. The hydrogen generation rate increased with an increasing Si content up to 10 wt% and was greater for the furnace-cooled samples than that for the quenched samples due to the more clearly formed eutectic structure.

  12. Performance of a beryllium copper nonmagnetic drill collar alloy

    SciTech Connect

    Dunlevey, F.

    1984-09-01

    Laboratory characterization and field testing show the advantages of beryllium copper Alloy 25 for use in non-magnetic drill collars, stabilizers, and subs. Beryllium copper is resistant to stress corrosion cracking failures at elevated temperature and pressure in the presence of hydrogen sulfide and dissolved chloride solutions. The alloy is more resistant than stainless steel to galling failure in threaded joints.

  13. Detection and quantification of solute clusters in a nanostructured ferritic alloy

    SciTech Connect

    Miller, Michael K.; Larson, David J.; Reinhard, D. A.

    2014-12-26

    A series of simulated atom probe datasets were examined with a friends-of-friends method to establish the detection efficiency required to resolve solute clusters in the ferrite phase of a 14YWT nanostructured ferritic alloy. The size and number densities of solute clusters in the ferrite of the as-milled mechanically-alloyed condition and the stir zone of a friction stir weld were estimated with a prototype high-detection-efficiency (~80%) local electrode atom probe. High number densities, 1.8 × 1024 m–3 and 1.2 × 1024 m–3, respectively of solute clusters containing between 2 and 9 solute atoms of Ti, Y and O and were detected for these two conditions. Furthermore, these results support first principle calculations that predicted that vacancies stabilize these Ti–Y–O– clusters, which retard diffusion and contribute to the excellent high temperature stability of the microstructure and radiation tolerance of nanostructured ferritic alloys.

  14. Detection and quantification of solute clusters in a nanostructured ferritic alloy

    DOE PAGES

    Miller, Michael K.; Larson, David J.; Reinhard, D. A.

    2014-12-26

    A series of simulated atom probe datasets were examined with a friends-of-friends method to establish the detection efficiency required to resolve solute clusters in the ferrite phase of a 14YWT nanostructured ferritic alloy. The size and number densities of solute clusters in the ferrite of the as-milled mechanically-alloyed condition and the stir zone of a friction stir weld were estimated with a prototype high-detection-efficiency (~80%) local electrode atom probe. High number densities, 1.8 × 1024 m–3 and 1.2 × 1024 m–3, respectively of solute clusters containing between 2 and 9 solute atoms of Ti, Y and O and were detectedmore » for these two conditions. Furthermore, these results support first principle calculations that predicted that vacancies stabilize these Ti–Y–O– clusters, which retard diffusion and contribute to the excellent high temperature stability of the microstructure and radiation tolerance of nanostructured ferritic alloys.« less

  15. Solute Enhanced Strain Hardening of Aluminum Alloys to Achieve Improved Combinations of Strength and Toughness

    NASA Astrophysics Data System (ADS)

    Hovanec, Christopher James

    2011-12-01

    The feasibility of achieving improved combinations of strength and toughness in aluminum alloy 2524 through solute enhanced strain hardening (SESH) has been explored in this study and shown to be viable. The effectiveness of SESH is directly dependent on the strain hardening rate (SHR) of the material being processed. Aluminum alloy 2524 naturally ages to the T4-temper after solution heat treating and quenching. The SHR of strain free and post cold rolled material as a function of natural aging time has been measured by means of simple compression. It has been determined that the SHR of AA2524 is more effective with solute in solution rather than clustered into GP zones. It has also been shown that the typical rapid formation of GP zones at room temperature (natural aging) is inhibited by moderate cold rolling strains (□CR ≥ 0.2) through dislocation aided vacancy annihilation. The practical limitations of quenching rate have been determined using hardness and eddy current electrical conductivity measurements. It has been shown that too slow of a quench rate results in solute being lost to both the formation of GP zones and embrittling precipitates during the quench, while too rapid of a quench rate results in mid-plane cracking of the work piece during the SESH processing. The mid-plane cracking was overcome by using an uphill quenching procedure to relieve residual stresses within the work piece. Aluminum alloy 2524 strengthened through SESH to a yield strength 11% greater than that in the T6-Temper exhibits: equivalent toughness, 5% greater UTS, 1% greater elongation, 7% greater R.A., and absorbs 15% more energy during tensile testing. At yield strengths comparable to published data for 2x24 alloys, the SESH 2524 exhibited up to a 60% increase in fracture toughness. The fractured surfaces of the SESH material exhibited transgranular dimpled rupture as opposed to the grain boundary ductile fracture (GBPF) observed in the artificially aged material.

  16. The long-term corrosion performance of Alloy 22 in heated brine solutions

    DOE PAGES

    Enos, D. G.; Bryan, C. R.

    2015-02-13

    Long-term corrosion experiments have been performed on Alloy 22 (UNS N06022), in a series of heated brines formulated to represent evaporatively concentrated ground water, to evaluate the long-term corrosion performance of the material. These solutions included 0.5 M NaCl, in addition to two simulated concentrated ground water solutions. Under conditions where Alloy 22 was anticipated to be passive, the corrosion rate was found to be vanishingly small (i.e., below the resolution of the weight-loss technique used to quantify corrosion in this study). However, under low pH conditions where Alloy 22 was anticipated to be active, or more specifically, where themore » chromium oxide passive film was not thermodynamically stable, the corrosion rate was appreciable. Furthermore, under such conditions the corrosion rate was observed to be a strong function of temperature, with an activation energy of 72.9±1.8 kJ/mol. Time of Flight-Secondary Ion Mass Spectroscopy analysis of the oxide layer revealed that, while sulfur was present within the oxide for all test conditions, no accumulation was observed at or near the metal/oxide interface. Furthermore, these observations confirm that inhibition of passive film formation via sulfur accumulation does not occur during the corrosion of Alloy 22.« less

  17. The long-term corrosion performance of Alloy 22 in heated brine solutions

    SciTech Connect

    Enos, D. G.; Bryan, C. R.

    2015-02-13

    Long-term corrosion experiments have been performed on Alloy 22 (UNS N06022), in a series of heated brines formulated to represent evaporatively concentrated ground water, to evaluate the long-term corrosion performance of the material. These solutions included 0.5 M NaCl, in addition to two simulated concentrated ground water solutions. Under conditions where Alloy 22 was anticipated to be passive, the corrosion rate was found to be vanishingly small (i.e., below the resolution of the weight-loss technique used to quantify corrosion in this study). However, under low pH conditions where Alloy 22 was anticipated to be active, or more specifically, where the chromium oxide passive film was not thermodynamically stable, the corrosion rate was appreciable. Furthermore, under such conditions the corrosion rate was observed to be a strong function of temperature, with an activation energy of 72.9±1.8 kJ/mol. Time of Flight-Secondary Ion Mass Spectroscopy analysis of the oxide layer revealed that, while sulfur was present within the oxide for all test conditions, no accumulation was observed at or near the metal/oxide interface. Furthermore, these observations confirm that inhibition of passive film formation via sulfur accumulation does not occur during the corrosion of Alloy 22.

  18. Influence of chemical disorder on energy dissipation and defect evolution in concentrated solid solution alloys

    DOE PAGES

    Zhang, Yanwen; Stocks, George Malcolm; Jin, Ke; ...

    2015-10-28

    A long-standing objective in materials research is to understand how energy is dissipated in both the electronic and atomic subsystems in irradiated materials, and how related non-equilibrium processes may affect defect dynamics and microstructure evolution. Here we show that alloy complexity in concentrated solid solution alloys having both an increasing number of principal elements and altered concentrations of specific elements can lead to substantial reduction in the electron mean free path and thermal conductivity, which has a significant impact on energy dissipation and consequentially on defect evolution during ion irradiation. Enhanced radiation resistance with increasing complexity from pure nickel tomore » binary and to more complex quaternary solid solutions is observed under ion irradiation up to an average damage level of 1 displacement per atom. Understanding how materials properties can be tailored by alloy complexity and their influence on defect dynamics may pave the way for new principles for the design of radiation tolerant structural alloys.« less

  19. The Effect of Solution Heat Treatment on an Advanced Nickel-Base Disk Alloy

    NASA Technical Reports Server (NTRS)

    Gayda, J.; Gabb, T. P.; Kantzos, P. T.

    2004-01-01

    Five heat treat options for an advanced nickel-base disk alloy, LSHR, have been investigated. These included two conventional solution heat treat cycles, subsolvus/oil quench and supersolvus/fan cool, which yield fine grain and coarse grain microstructure disks respectively, as well as three advanced dual microstructure heat treat (DMHT) options. The DMHT options produce disks with a fine grain bore and a coarse grain rim. Based on an overall evaluation of the mechanical property data, it was evident that the three DMHT options achieved a desirable balance of properties in comparison to the conventional solution heat treatments for the LSHR alloy. However, one of the DMHT options, SUB/DMHT, produced the best set of properties, largely based on dwell crack growth data. Further evaluation of the SUB/DMHT option in spin pit experiments on a generic disk shape demonstrated the advantages and reliability of a dual grain structure at the component level.

  20. Stability of the grain structure in 2219-O aluminum alloy friction stir welds during solution treatment

    SciTech Connect

    Chen, Y.C. . E-mail: armstrong@hit.edu.cn; Feng, J.C.; Liu, H.J.

    2007-02-15

    The stability of the grain structure in 2219-O aluminum alloy friction stir welds during solution treatment has been investigated. Experimental results show that the solution treatment causes drastic grain growth, Grain growth initiates at the surface and the bottom of the weld and then extends to the weld centre within several minutes. The solution treatment temperature and the welding heat input have a significant effect on grain growth. The higher the solution temperature, or the higher the welding heat input, the greater the grain growth. The instability of the grains is attributed to an imbalance between thermodynamic driving forces for grain growth and the pinning forces impeding grain boundary migration during solution treatment.

  1. Investigation of compositional segregation during unidirectional solidification of solid solution semiconducting alloys

    NASA Technical Reports Server (NTRS)

    Wang, J. C.

    1982-01-01

    Compositional segregation of solid solution semiconducting alloys in the radial direction during unidirectional solidification was investigated by calculating the effect of a curved solid liquid interface on solute concentration at the interface on the solid. The formulation is similar to that given by Coriell, Boisvert, Rehm, and Sekerka except that a more realistic cylindrical coordinate system which is moving with the interface is used. Analytical results were obtained for very small and very large values of beta with beta = VR/D, where V is the velocity of solidification, R the radius of the specimen, and D the diffusivity of solute in the liquid. For both very small and very large beta, the solute concentration at the interface in the solid C(si) approaches C(o) (original solute concentration) i.e., the deviation is minimal. The maximum deviation of C(si) from C(o) occurs for some intermediate value of beta.

  2. Effect of Solution Annealing Temperatures on the Crevice Corrosion Mode of Alloy 22

    SciTech Connect

    El-Dasher, B S; Etien, R; Torres, S G

    2005-10-31

    The effect of solution annealing temperature on the observed corrosion attack mode in Alloy 22 welds was assessed. Three types of specimens were examined, including the as-welded state, solution annealed for 20 minutes at 1121 C, and solution annealed for 20 minutes at 1200 C. The microstructures of the specimens were first mapped using electron backscatter diffraction to determine the grain structure evolution due to solution annealing. The specimens were then subjected to electrochemical testing in a 6 molal NaCl + 0.9 molal KNO{sub 3} environment to initiate crevice corrosion. Examination of the specimen surfaces after corrosion testing showed that in the as-welded specimen, corrosion was present in both the weld dendrites as well as around the secondary phases. However, the specimen solution annealed at 1121 C showed corrosion only at secondary phases and the specimen annealed at 1200 C showed pitting corrosion only in a handful of grains.

  3. Dissolved plume attenuation with DNAPL source remediation, aqueous decay and volatilization — Analytical solution, model calibration and prediction uncertainty

    NASA Astrophysics Data System (ADS)

    Parker, Jack C.; Park, Eungyu; Tang, Guoping

    2008-11-01

    A vertically-integrated analytical model for dissolved phase transport is described that considers a time-dependent DNAPL source based on the upscaled dissolution kinetics model of Parker and Park with extensions to consider time-dependent source zone biodecay, partial source mass reduction, and remediation-enhanced source dissolution kinetics. The model also considers spatial variability in aqueous plume decay, which is treated as the sum of aqueous biodecay and volatilization due to diffusive transport and barometric pumping through the unsaturated zone. The model is implemented in Excel/VBA coupled with (1) an inverse solution that utilizes prior information on model parameters and their uncertainty to condition the solution, and (2) an error analysis module that computes parameter covariances and total prediction uncertainty due to regression error and parameter uncertainty. A hypothetical case study is presented to evaluate the feasibility of calibrating the model from limited noisy field data. The results indicate that prediction uncertainty increases significantly over time following calibration, primarily due to propagation of parameter uncertainty. However, differences between the predicted performance of source zone partial mass reduction and the known true performance were reasonably small. Furthermore, a clear difference is observed between the predicted performance for the remedial action scenario versus that for a no-action scenario, which is consistent with the true system behavior. The results suggest that the model formulation can be effectively utilized to assess monitored natural attenuation and source remediation options if careful attention is given to model calibration and prediction uncertainty issues.

  4. Mechanisms controlling the production and transport of methane, carbon dioxide, and dissolved solutes within a boreal peatland

    SciTech Connect

    Siegel, D.I.

    1992-04-09

    Peatlands are one of the most important terrestrial reservoirs in the global cycle for carbon, and are a major source for atmospheric methane. However, little is known about the dynamics of these carbon reservoirs or their feedback mechanisms with the pool of atmospheric CO{sub 2} during the Holocene. Specifically, it is unknown whether large peat basins are sources, sinks, or steady-state reservoirs for the global carbon cycle. In particular, the production and transport of methane, carbon dioxide, and dissolved organic carbon form the deeper portions of these peatlands is unknown. Our DOE research program is to conduct an integrated ecologic and hydrogeochemical study of the Glacial Lake Agassiz peatlands (northern Minnesota) to better understand the carbon dynamics in globally significant peat basins. Specifically, our study will provide local and regional data on (1), rates of carbon accumulation and loss and fluxes of methane in the peat profiles; (2) the physical and botanical factors controlling the production of methane and carbon dioxide in the wetland; and (3) the role of hydrogeologic processes in controlling the fluxes of gases and solutes through the peat. We intend to use computer simulation models, calibrated to field data, to scale-up from local to regional estimates of methane and carbon dioxide within the basin. How gases and dissolved organic carbon escapes form peatlands in unknown. It has been suggested that the concentrations of methane produced in the upper peat are sufficient to produce diffusion gradients towards the surface. Alternatively, gas may move through the peat profile by groundwater advection.

  5. Nanobubble clusters of dissolved gas in aqueous solutions of electrolyte. II. Theoretical interpretation

    NASA Astrophysics Data System (ADS)

    Bunkin, N. F.; Shkirin, A. V.

    2012-08-01

    A quantitative model of ion-stabilized gas bubbles is suggested. Charging the bubbles by the ions, which are capable of adsorption, and the screening by a cloud of counter-ions, which are less absorptable, is modeled. It is shown that, subject to the charge of bubble, two regimes of such screening can be realized. For low-charged bubbles, the screening is described in the framework of the known linearized Debye-Huckel approach, when the sign of the counter-ion cloud is preserved everywhere in the liquid, whereas at large charge this sign is changed at some distance from the bubble surface. This effect provides the mechanism for the emergence of two types of compound particles having the opposite polarity, which leads to the aggregation of such compound particles into fractal clusters. Based on experimental data, arguments in favor of the existence of the clusters composed of the ion-stabilized bubbles in aqueous electrolyte solutions are advanced. This paper provides theoretical grounds for the experimental results presented in the previous paper (part I) published in this journal.

  6. Gamma prime precipitation mechanisms and solute partitioning in Ni-base alloys

    NASA Astrophysics Data System (ADS)

    Rojhirunsakool, Tanaporn

    Nickel-base superalloys have been emerged as materials for gas turbines used for jet propulsion and electricity generation. The strength of the superalloys depends mainly from an ordered precipitates of L12 structure, so called gamma prime (gamma') dispersed within the disorder gamma matrix. The Ni-base alloys investigated in this dissertation comprise both model alloy systems based on Ni-Al-Cr and Ni-Al-Co as well as the commercial alloy Rene N5. Classical nucleation and growth mechanism dominates the gamma' precipitation process in slowed-cooled Ni-Al-Cr alloys. The effect of Al and Cr additions on gamma' precipitate size distribution as well as morphological and compositional development of gamma' precipitates were characterized by coupling transmission electron microscopy (TEM) and 3D atom probe (3DAP) techniques. Rapid quenching Ni-Al-Cr alloy experiences a non-classical precipitation mechanism. Structural evolution of the gamma' precipitates formed and subsequent isothermal annealing at 600 °C were investigated by coupling TEM and synchrotron-based high-energy xray diffraction (XRD). Compositional evolution of the non-classically formed gamma' precipitates was determined by 3DAP and Langer, Bar-on and Miller (LBM) method. Besides homogeneous nucleation, the mechanism of heterogeneous gamma' precipitation involving a discontinuous precipitation mechanism, as a function of temperature, was the primary focus of study in case of the Ni-Al-Co alloy. This investigation coupled SEM, SEM-EBSD, TEM and 3DAP techniques. Lastly, solute partitioning and enrichment of minor refractory elements across/at the gamma/ gamma' interfaces in the commercially used single crystal Rene N5 superalloy was investigated by using an advantage of nano-scale composition investigation of 3DAP technique.

  7. Hydrogen embrittlement of work-hardened Ni-Ti alloy in fluoride solutions.

    PubMed

    Yokoyama, Ken'ichi; Kaneko, Kazuyuki; Ogawa, Toshio; Moriyama, Keiji; Asaoka, Kenzo; Sakai, Jun'ichi

    2005-01-01

    Hydrogen embrittlement of work-hardened Ni-Ti alloy has been examined in acidulated phosphate fluoride (APF) solutions. Upon immersion in a 2.0% APF solution with a pH of 5.0, tensile strength decreased markedly with immersion time. Moreover, the fracture mode changed from ductile to brittle due to brittle layer formation at the peripheral part of the cross section of the specimen. The amount of absorbed hydrogen increased linearly with immersion time, and it reached above 5000 mass ppm after 24 h. The hydrogen desorption temperature of the immersed specimens shifted from 450 degrees C to a lower temperature with immersion time. As the amount of absorbed hydrogen was larger than 500 mass ppm, the degradation of mechanical properties was recognized. Although the tensile properties and fracture mode scarcely change in a 0.2% APF solution, the slight reduction in hardness and hydrogen absorption of several hundreds mass ppm were observed. The results of the present study imply that work-hardened Ni-Ti alloy is less sensitive to hydrogen embrittlement compared with Ni-Ti superelastic alloy.

  8. Temperature Dependence of the Mechanical Properties of Equiatomic Solid Solution Alloys with FCC Crystal Structures

    DOE PAGES

    Wu, Zhenggang; Bei, Hongbin; Pharr, George M.; ...

    2014-10-03

    We found that compared to decades-old theories of strengthening in dilute solid solutions, the mechanical behavior of concentrated solid solutions is relatively poorly understood. A special subset of these materials includes alloys in which the constituent elements are present in equal atomic proportions, including the high-entropy alloys of recent interest. A unique characteristic of equiatomic alloys is the absence of “solvent” and “solute” atoms, resulting in a breakdown of the textbook picture of dislocations moving through a solvent lattice and encountering discrete solute obstacles. Likewise, to clarify the mechanical behavior of this interesting new class of materials, we investigate heremore » a family of equiatomic binary, ternary and quaternary alloys based on the elements Fe, Ni, Co, Cr and Mn that were previously shown to be single-phase face-centered cubic (fcc) solid solutions. The alloys were arc-melted, drop-cast, homogenized, cold-rolled and recrystallized to produce equiaxed microstructures with comparable grain sizes. Tensile tests were performed at an engineering strain rate of 10-3 s-1 at temperatures in the range 77–673 K. Unalloyed fcc Ni was processed similarly and tested for comparison. The flow stresses depend to varying degrees on temperature, with some (e.g. NiCoCr, NiCoCrMn and FeNiCoCr) exhibiting yield and ultimate strengths that increase strongly with decreasing temperature, while others (e.g. NiCo and Ni) exhibit very weak temperature dependencies. Moreover, to better understand this behavior, the temperature dependencies of the yield strength and strain hardening were analyzed separately. Lattice friction appears to be the predominant component of the temperature-dependent yield stress, possibly because the Peierls barrier height decreases with increasing temperature due to a thermally induced increase of dislocation width. In the early stages of plastic flow (5–13% strain, depending on material), the temperature

  9. Temperature Dependence of the Mechanical Properties of Equiatomic Solid Solution Alloys with FCC Crystal Structures

    SciTech Connect

    Wu, Zhenggang; Bei, Hongbin; Pharr, George M.; George, Easo P.

    2014-10-03

    We found that compared to decades-old theories of strengthening in dilute solid solutions, the mechanical behavior of concentrated solid solutions is relatively poorly understood. A special subset of these materials includes alloys in which the constituent elements are present in equal atomic proportions, including the high-entropy alloys of recent interest. A unique characteristic of equiatomic alloys is the absence of “solvent” and “solute” atoms, resulting in a breakdown of the textbook picture of dislocations moving through a solvent lattice and encountering discrete solute obstacles. Likewise, to clarify the mechanical behavior of this interesting new class of materials, we investigate here a family of equiatomic binary, ternary and quaternary alloys based on the elements Fe, Ni, Co, Cr and Mn that were previously shown to be single-phase face-centered cubic (fcc) solid solutions. The alloys were arc-melted, drop-cast, homogenized, cold-rolled and recrystallized to produce equiaxed microstructures with comparable grain sizes. Tensile tests were performed at an engineering strain rate of 10-3 s-1 at temperatures in the range 77–673 K. Unalloyed fcc Ni was processed similarly and tested for comparison. The flow stresses depend to varying degrees on temperature, with some (e.g. NiCoCr, NiCoCrMn and FeNiCoCr) exhibiting yield and ultimate strengths that increase strongly with decreasing temperature, while others (e.g. NiCo and Ni) exhibit very weak temperature dependencies. Moreover, to better understand this behavior, the temperature dependencies of the yield strength and strain hardening were analyzed separately. Lattice friction appears to be the predominant component of the temperature-dependent yield stress, possibly because the Peierls barrier height decreases with increasing temperature due to a thermally induced increase of dislocation width. In the early stages of plastic flow (5–13% strain, depending on material), the

  10. Effect of synovial fluid, phosphate-buffered saline solution, and water on the dissolution and corrosion properties of CoCrMo alloys as used in orthopedic implants.

    PubMed

    Lewis, A C; Kilburn, M R; Papageorgiou, I; Allen, G C; Case, C P

    2005-06-15

    The corrosion and dissolution of high- and low-carbon CoCrMo alloys, as used in orthopedic joint replacements, were studied by immersing samples in phosphate-buffered saline (PBS), water, and synovial fluid at 37 degrees C for up to 35 days. Bulk properties were analyzed with a fine ion beam microscope. Surface analyses by X-ray photoelectron spectroscopy and Auger electron spectroscopy showed surprisingly that synovial fluid produced a thin oxide/hydroxide layer. Release of ions into solution from the alloy also followed an unexpected pattern where synovial fluid, of all the samples, had the highest Cr concentration but the lowest Co concentration. The presence of carbide inclusions in the alloy did not affect the corrosion or the dissolution mechanisms, although the carbides were a significant feature on the metal surface. Only one mechanism was recognized as controlling the thickness of the oxide/hydroxide interface. The analysis of the dissolved metal showed two mechanisms at work: (1) a protein film caused ligand-induced dissolution, increasing the Cr concentration in synovial fluid, and was explained by the equilibrium constants; (2) corrosion at the interface increased the Co in PBS. The effect of prepassivating the samples (ASTM F-86-01) did not always have the desired effect of reducing dissolution. The release of Cr into PBS increased after prepassivation. The metal-synovial fluid interface did not contain calcium phosphate as a deposit, typically found where samples are exposed to calcium rich bodily fluids. (c) 2005 Wiley Periodicals, Inc.

  11. Effect of solutes in binary columbium /Nb/ alloys on creep strength

    NASA Technical Reports Server (NTRS)

    Klein, M. J.; Metcalfe, A. G.

    1973-01-01

    The effect of seven different solutes in binary columbium (Nb) alloys on creep strength was determined from 1400 to 3400 F for solute concentrations to 20 at.%, using a new method of creep-strength measurement. The technique permits rapid determination of approximate creep strength over a large temperature span. All of the elements were found to increase the creep strength of columbium except tantalum. This element did not strengthen columbium until the concentration exceeded 10 at.%. Hafnium, zirconium, and vanadium strengthed columbium most at low temperatures and concentrations, whereas tungsten, molybdenum, and rhenium contributed more to creep strength at high temperatures and concentrations.

  12. Effect of solutes in binary columbium /Nb/ alloys on creep strength

    NASA Technical Reports Server (NTRS)

    Klein, M. J.; Metcalfe, A. G.

    1973-01-01

    The effect of seven different solutes in binary columbium (Nb) alloys on creep strength was determined from 1400 to 3400 F for solute concentrations to 20 at.%, using a new method of creep-strength measurement. The technique permits rapid determination of approximate creep strength over a large temperature span. All of the elements were found to increase the creep strength of columbium except tantalum. This element did not strengthen columbium until the concentration exceeded 10 at.%. Hafnium, zirconium, and vanadium strengthed columbium most at low temperatures and concentrations, whereas tungsten, molybdenum, and rhenium contributed more to creep strength at high temperatures and concentrations.

  13. Swelling of solute-modified Fe-Cr-Mn alloys in FFTF (Fast Flux Test Facility)-MOTA

    SciTech Connect

    Garner, F.A.

    1986-10-01

    Density change data continue to be accumulated on solute-modified and commercial Fe-Cr-Mn alloys irradiated at 520/sup 0/C and 50 dpa. The tendency toward saturation of density change observed in the simple ternary alloys in the annealed condition is accentuated by cold-working and solute addition. Irradiation at 420/sup 0/C appears to further accelerate the tendency toward saturation.

  14. Aqueous photochemical degradation of BDE-153 in solutions with natural dissolved organic matter.

    PubMed

    Wang, Huili; Wang, Mei; Wang, Hui; Gao, Jiajia; Dahlgren, Randy A; Yu, Qing; Wang, Xuedong

    2016-07-01

    The compound 2,2',4,4',5,5'-hexabrominated diphenyl ether (BDE-153) is an intermediate photolytic product in the degradation of highly brominated diphenyl ethers to lower brominated forms. Herein, we report the effects of two natural organic matter (NOM) sources, Suwannee River fulvic acid (SRFA) and Pony Lake fulvic acid (PLFA), on BDE-153 photolysis in water. The rate constant (k) and half-life of BDE-153 was 2.26 × 10(-2) min(-1) and 30.72 min under UV-Vis irradiation (direct photolysis at λ > 290 nm). The k value for BDE-153 decreased markedly in the presence of NOM with a larger decrease in the presence of PLFA than SRFA. Electron spin resonance (ESR) demonstrated generation of free radicals in the photolytic process that mainly involved (1)O2 and OH. The biomolecular k values for reaction of (1)O2 and OH with BDE-153 were 3.65 × 10(6) and 7.70 × 10(8) M(-1) s(-1), respectively. The contribution of OH (28.7-31.0%) to the indirect photolysis of BDE-153 was higher than for (1)O2 (12.9-14.9%). The photolytic rate of BDE-153 in oxygen-rich (aerated) solution was much slower than in oxygen-poor (nitrogen-sparged) conditions, demonstrating that (3)NOM* is a more effective reagent for degradation of BDE-153 than (1)O2. Addition of sorbic acid (a (3)NOM* quencher) significantly reduced the photolytic rate of BDE-153 confirming the important role of (3)NOM* in indirect photolysis. In the presence of NOM, BDE-153 indirect photolysis was facilitated mainly by reaction with (3)NOM* and OH. To the best of our knowledge, this is the first comprehensive investigation of indirect photolysis of BDE-153 in water containing NOM. Copyright © 2016 Elsevier Ltd. All rights reserved.

  15. Catalytic role of iron in the formation of silver nanoparticles in photo-irradiated Ag(+)-dissolved organic matter solution.

    PubMed

    Yin, Yongguang; Han, Dan; Tai, Chao; Tan, Zhiqiang; Zhou, Xiaoxia; Yu, Sujuan; Liu, Jingfu; Jiang, Guibin

    2017-06-01

    Photo-reduction of Ag(+) to silver nanoparticle (AgNPs) by dissolved organic matter (DOM) is a possible source of naturally occurring AgNPs. However, how this photo-reduction process is influenced by ubiquitous metal ions is still not well understood. In addition, in previous studies, the formation of AgNPs in DOM solution was usually monitored by UV-Vis spectroscopy, and there is still lack of quantitative analysis for the formed AgNPs. In the present study, the role of Fe(2+)/Fe(3+) at environmental concentration level on this photochemical process was investigated, and the enhanced formation of AgNPs by Fe(2+)/Fe(3+) was probed and quantified by using UV-Vis spectroscopy, transmission electron microscopy, and liquid chromatography-inductively coupled plasma mass spectrometry. It was demonstrated that while Fe(3+) can oxidize AgNPs to release Ag(+), Fe(2+) can reduce Ag(+) into AgNPs. However, the DOM-induced reduction of Fe(3+) makes iron an effective electron shuttle between DOM and Ag(+), and both Fe(2+) and Fe(3+) enhanced AgNP formation. The impacts of environmentally relevant factors, including DOM concentration and solution pH, on this process were studied comprehensively, which showed that the catalytic role of iron was more significant at higher DOM concentration and lower pH. This iron-enhanced formation of AgNPs in photo-irradiated Ag(+)-DOM solution have great environmental implications on the formation of natural AgNPs and the transformation of engineered AgNPs in acidic surface water with high iron content. Copyright © 2017 Elsevier Ltd. All rights reserved.

  16. Factors controlling the chemical composition of colloidal and dissolved fractions in soil solutions and the mobility of trace elements in soils

    NASA Astrophysics Data System (ADS)

    Gangloff, Sophie; Stille, Peter; Schmitt, Anne-Désirée; Chabaux, François

    2016-09-01

    The objectives of this study were to determine the processes and physico-chemical conditions that affect the composition of the soil solutions of a forest soil and to elucidate their impact on the transport of major and trace elements through the colloidal (0.2 μm to 5 kDa) and dissolved (<5 kDa) fractions in the first meter of soil. All experiments were performed with soil solutions obtained using lysimeter plates situated on an experimental spruce parcel of the Strengbach catchment (Northeastern France). The surface samples filtered at 0.2 μm facilitated the examination of the influence of litter decomposition on the chemical composition of the upper soil solutions. The impact of the soils biogeochemical conditions (pH, moisture, temperature, oxic or anoxic conditions) on litter decomposition was also examined. More particularly, the increase in NH4+ and NO2- compounds in some of the soil solutions points to denitrification processes in an anoxic environment. Thus, under anoxic conditions, the soil solution is enriched in Ca, P, Mn and Zn, whereas under oxic conditions it is enriched in Al and Fe. The physico-chemical conditions are more seasonally dependent in the upper soil horizons than in the deeper ones and have an impact on the variability of the chemical composition of the soil solutions. The colloidal and dissolved fractions of the soil solutions were obtained by tangential flow ultra-filtration. The experimental results reveal that nutrients, such as NO3- and P, are primarily in the dissolved fraction and consequently bioavailable; secondary minerals may be dissolved and/or precipitate in the colloidal fraction, such as pyromorphite (Pb5(PO4)3(OH, Cl, F)). The results further indicate that microbial activity influences the composition of the colloidal and dissolved fractions, and possibly enriches the colloidal fraction in Ca, Mn and P, diminishes the concentrations of Pb, V, Cr and Fe in the dissolved fraction, and changes the structure of organic

  17. Unique Challenges for Modeling Defect Dynamics in Concentrated Solid-Solution Alloys

    NASA Astrophysics Data System (ADS)

    Zhao, Shijun; Weber, William J.; Zhang, Yanwen

    2017-07-01

    Recently developed concentrated solid solution alloys (CSAs) are shown to have improved performance under irradiation that depends strongly on the number of alloying elements, alloying species, and their concentrations. In contrast to conventional dilute alloys, CSAs are composed of multiple principal elements situated randomly in a simple crystalline lattice. As a result, the intrinsic disorder has a profound influence on energy dissipation pathways and defect evolution when these CSAs are subjected to energetic particle irradiation. Extraordinary irradiation resistance, including suppression of void formation by two orders of magnitude at an elevated temperature, has been achieved with increasing compositional complexity in CSAs. Unfortunately, the loss of translational invariance associated with the intrinsic chemical disorder poses great challenges to theoretical modeling at the electronic and atomic levels. Based on recent computer simulation results for a set of novel Ni-containing, face-centered cubic CSAs, we review theoretical modeling progress in handling disorder in CSAs and underscore the impact of disorder on defect dynamics. We emphasize in particular the unique challenges associated with the description of defect dynamics in CSAs.

  18. Effects of Solute Concentrations on Kinetic Pathways in Ni-Al-Cr Alloys

    NASA Technical Reports Server (NTRS)

    Booth-Morrison, Christopher; Weninger, Jessica; Sudbrack, Chantal K.; Mao, Zugang; Seidman, David N.; Noebe, Ronald D.

    2008-01-01

    The kinetic pathways resulting from the formation of coherent gamma'-precipitates from the gamma-matrix are studied for two Ni-Al-Cr alloys with similar gamma'-precipitate volume fractions at 873 K. The details of the phase decompositions of Ni-7.5Al-8.5Cr at.% and Ni-5.2Al-14.2Cr at.% for aging times from 1/6 to 1024 h are investigated by atom-probe tomography, and are found to differ significantly from a mean-field description of coarsening. The morphologies of the gamma'-precipitates of the alloys are similar, though the degrees of gamma'-precipitate coagulation and coalescence differ. Quantification within the framework of classical nucleation theory reveals that differences in the chemical driving forces for phase decomposition result in differences in the nucleation behavior of the two alloys. The temporal evolution of the gamma'-precipitate average radii and the gamma-matrix supersaturations follow the predictions of classical coarsening models. The compositional trajectories of the gamma-matrix phases of the alloys are found to follow approximately the equilibrium tie-lines, while the trajectories of the gamma'-precipitates do not, resulting in significant differences in the partitioning ratios of the solute elements.

  19. Inelasticity and precipitation of germanium from a solid solution in Al-Ge binary alloys

    NASA Astrophysics Data System (ADS)

    Kardashev, B. K.; Korchunov, B. N.; Nikanorov, S. P.; Osipov, V. N.

    2015-08-01

    The influence of precipitation of germanium atoms in a solid solution on the dependence of the inelasticity characteristics on the germanium content in aluminum-germanium alloys prepared by directional crystallization has been studied. It has been shown that the Young's modulus defect, the amplitude-dependent decrement, and the microplastic flow stress at a specified cyclic strain amplitude have extreme values at the eutectic germanium content in the alloy. The eutectic composition of the alloy undergoes a ductilebrittle transition. It has been found that there is a correlation between the dependences of the Young's modulus defect, amplitude-dependent decrement, microplastic flow stress, and specific entropy of the exothermal process of germanium precipitation on the germanium content in the hypoeutectic alloy. The concentration dependences of the inelasticity characteristics and their changes after annealing have been explained by the change in the resistance to the motion of intragrain dislocations due to different structures of the Guinier-Preston zones formed during the precipitation of germanium atoms.

  20. Thermodynamic and kinetic destabilization of magnesium hydride using Mg-In solid solution alloys.

    PubMed

    Zhou, Chengshang; Fang, Zhigang Zak; Lu, Jun; Zhang, Xiaoyi

    2013-07-31

    Efforts to thermodynamically destabilize magnesium hydride (MgH2), so that it can be used for practical hydrogen storage applications, have been a difficult challenge that has eluded scientists for decades. This letter reports that MgH2 can indeed be destabilized by forming solid solution alloys of magnesium with group III and IVB elements, such as indium. Results of this research showed that the equilibrium hydrogen pressure of a Mg-0.1In alloy is 70% higher than that of pure MgH2. The temperature at 1 bar hydrogen pressure (T1bar) of Mg-0.1In alloy was reduced to 262.9 °C from 278.9 °C, which is the T1bar of pure MgH2. Furthermore, the kinetic rates of dehydrogenation of Mg-0.1In alloy hydride doped with a titanium intermetallic (TiMn2) catalyst were also significantly improved compared with those of MgH2.

  1. Effects of Solute Concentrations on Kinetic Pathways in Ni-Al-Cr Alloys

    NASA Technical Reports Server (NTRS)

    Booth-Morrison, Christopher; Weninger, Jessica; Sudbrack, Chantal K.; Mao, Zugang; Seidman, David N.; Noebe, Ronald D.

    2008-01-01

    The kinetic pathways resulting from the formation of coherent gamma'-precipitates from the gamma-matrix are studied for two Ni-Al-Cr alloys with similar gamma'-precipitate volume fractions at 873 K. The details of the phase decompositions of Ni-7.5Al-8.5Cr at.% and Ni-5.2Al-14.2Cr at.% for aging times from 1/6 to 1024 h are investigated by atom-probe tomography, and are found to differ significantly from a mean-field description of coarsening. The morphologies of the gamma'-precipitates of the alloys are similar, though the degrees of gamma'-precipitate coagulation and coalescence differ. Quantification within the framework of classical nucleation theory reveals that differences in the chemical driving forces for phase decomposition result in differences in the nucleation behavior of the two alloys. The temporal evolution of the gamma'-precipitate average radii and the gamma-matrix supersaturations follow the predictions of classical coarsening models. The compositional trajectories of the gamma-matrix phases of the alloys are found to follow approximately the equilibrium tie-lines, while the trajectories of the gamma'-precipitates do not, resulting in significant differences in the partitioning ratios of the solute elements.

  2. Solidification of a binary alloy: Finite-element, single-domain simulation and new benchmark solutions

    NASA Astrophysics Data System (ADS)

    Le Bars, Michael; Worster, M. Grae

    2006-07-01

    A finite-element simulation of binary alloy solidification based on a single-domain formulation is presented and tested. Resolution of phase change is first checked by comparison with the analytical results of Worster [M.G. Worster, Solidification of an alloy from a cooled boundary, J. Fluid Mech. 167 (1986) 481-501] for purely diffusive solidification. Fluid dynamical processes without phase change are then tested by comparison with previous numerical studies of thermal convection in a pure fluid [G. de Vahl Davis, Natural convection of air in a square cavity: a bench mark numerical solution, Int. J. Numer. Meth. Fluids 3 (1983) 249-264; D.A. Mayne, A.S. Usmani, M. Crapper, h-adaptive finite element solution of high Rayleigh number thermally driven cavity problem, Int. J. Numer. Meth. Heat Fluid Flow 10 (2000) 598-615; D.C. Wan, B.S.V. Patnaik, G.W. Wei, A new benchmark quality solution for the buoyancy driven cavity by discrete singular convolution, Numer. Heat Transf. 40 (2001) 199-228], in a porous medium with a constant porosity [G. Lauriat, V. Prasad, Non-darcian effects on natural convection in a vertical porous enclosure, Int. J. Heat Mass Transf. 32 (1989) 2135-2148; P. Nithiarasu, K.N. Seetharamu, T. Sundararajan, Natural convective heat transfer in an enclosure filled with fluid saturated variable porosity medium, Int. J. Heat Mass Transf. 40 (1997) 3955-3967] and in a mixed liquid-porous medium with a spatially variable porosity [P. Nithiarasu, K.N. Seetharamu, T. Sundararajan, Natural convective heat transfer in an enclosure filled with fluid saturated variable porosity medium, Int. J. Heat Mass Transf. 40 (1997) 3955-3967; N. Zabaras, D. Samanta, A stabilized volume-averaging finite element method for flow in porous media and binary alloy solidification processes, Int. J. Numer. Meth. Eng. 60 (2004) 1103-1138]. Finally, new benchmark solutions for simultaneous flow through both fluid and porous domains and for convective solidification processes are

  3. Fretting properties of biodegradable Mg-Nd-Zn-Zr alloy in air and in Hank’s solution

    NASA Astrophysics Data System (ADS)

    Li, Wenting; Li, Nan; Zheng, Yufeng; Yuan, Guangyin

    2016-11-01

    Fretting is a significant cause for the failure of orthopedic implants. Currently, since magnesium and its alloys have been developed as promising biodegradable implant materials, the fretting behavior of the Mg alloys is of great research significance. In this study, a Mg-Nd-Zn-Zr alloy (hereafter, denoted as JDBM alloy) was selected as experimental material, and its fretting behaviors were evaluated under 5 N, 10 N and 20 N normal loads with a displacement of 200 μm under the frequency of 10 Hz at 37 °C in air and in Hank’s solution, respectively. The results indicated that while the friction coefficient decreased with the increment of the normal load, the wear volume of the alloy increased with the increment of the normal load both in air and in Hank’s solution. Both the friction coefficients and the wear volume of the fretting in Hank’s solution were much lower than those in air environment. The evolution trend of friction coefficients with time had different performance in air environment and the Hank’s solution group. Although oxidation occurred during the fretting tests in Hank’s solution, the damage of JDBM alloy was still reduced due to the lubrication effects of Hank’s solution. Moreover, the addition of Fetal bovine serum (FBS) could act as lubrication and result in the reduction of the fretting damage.

  4. Fretting properties of biodegradable Mg-Nd-Zn-Zr alloy in air and in Hank’s solution

    PubMed Central

    Li, Wenting; Li, Nan; Zheng, Yufeng; Yuan, Guangyin

    2016-01-01

    Fretting is a significant cause for the failure of orthopedic implants. Currently, since magnesium and its alloys have been developed as promising biodegradable implant materials, the fretting behavior of the Mg alloys is of great research significance. In this study, a Mg-Nd-Zn-Zr alloy (hereafter, denoted as JDBM alloy) was selected as experimental material, and its fretting behaviors were evaluated under 5 N, 10 N and 20 N normal loads with a displacement of 200 μm under the frequency of 10 Hz at 37 °C in air and in Hank’s solution, respectively. The results indicated that while the friction coefficient decreased with the increment of the normal load, the wear volume of the alloy increased with the increment of the normal load both in air and in Hank’s solution. Both the friction coefficients and the wear volume of the fretting in Hank’s solution were much lower than those in air environment. The evolution trend of friction coefficients with time had different performance in air environment and the Hank’s solution group. Although oxidation occurred during the fretting tests in Hank’s solution, the damage of JDBM alloy was still reduced due to the lubrication effects of Hank’s solution. Moreover, the addition of Fetal bovine serum (FBS) could act as lubrication and result in the reduction of the fretting damage. PMID:27812007

  5. Discoloration and dissolution of titanium and titanium alloys with immersion in peroxide- or fluoride-containing solutions.

    PubMed

    Noguchi, Tatsumi; Takemoto, Shinji; Hattori, Masayuki; Yoshinari, Masao; Kawada, Eiji; Oda, Yutaka

    2008-01-01

    This study compared differences in discoloration and dissolution in several titanium alloys with immersion in peroxide- or fluoride-containing solution. Commercially pure titanium (CP-Ti) and six titanium-based alloys were used: Ti-0.15Pd, Ti-6Al-4V, Ti-7Nb-6Al, Ti-55Ni, Ti-10Cu, and Ti-20Cr. Two test solutions were prepared for immersion of polished titanium and titanium alloys: one consisting of 0.2% NaF + 0.9% NaCl (pH 3.8 with lactic acid) and the other of 0.1 mol/l H2O2 + 0.9% NaCl (pH 5.5). Following immersion, color changes were determined with a color meter and released elements were measured using ICP-OES. Discoloration and dissolution rates differed between the two solutions. In the hydrogen peroxide-containing solution, color difference was higher in Ti-55Ni and Ti-6Al-4V than in any of the other alloys, and that Ti-55Ni showed the highest degree of dissolution. In the acidulated fluoride-containing solution, CP-Ti, Ti-0.15Pd, Ti-6Al-4V, Ti-7Nb-6Al, and Ti-10Cu alloys showed remarkable discoloration and dissolution with immersion. On the contrary, Ti-20Cr alloy showed very little discoloration and dissolution in either solution.

  6. Role of Dissolved and Molecular Oxygen on Cu and PtCu Alloy Particle Structure during Laser Ablation Synthesis in Liquids.

    PubMed

    Marzun, Galina; Bönnemann, Helmut; Lehmann, Christian; Spliethoff, Bernd; Weidenthaler, Claudia; Barcikowski, Stephan

    2017-05-05

    The role of molecular oxygen dissolved in the solvent is often discussed as being an influential factor on particle oxidation during pulsed laser ablation in liquids. However, the formation of the particles during laser synthesis takes place under extreme conditions that enable the decomposition of the liquid medium. Reactive species of the solvent may then affect particle formation due to a chemical reaction in the reactive plasma. Experimental results show a difference between the role of dissolved molecular oxygen and the contribution from the oxygen in water molecules. Using a metallic Cu target in air-saturated water, laser ablation led to 20.5 wt % Cu, 11.5 wt % Cu2 O, and 68 wt % CuO nanoparticles, according to X-ray diffraction results. In contrast to particles obtained in air-saturated water, no CuO was observed in the colloid synthesized in a Schlenk ablation chamber in completely oxygen-free water. Under these conditions, less-oxidized nanoparticles (25 wt % Cu and 75 wt % Cu2 O) were synthesized. The results show that nanoparticle oxidation during laser synthesis is mainly caused by reactive oxygen species from the decomposition of water molecules. However, the addition of molecular oxygen promotes particle oxidation. Storage of the Cu colloid in the presence of dissolved oxygen leads, due to aging, to nanostructures with a higher oxidation state than the freshly prepared colloid. The XRD pattern of the sample prepared in air-saturated acetone showed no crystalline phases, which is possibly due to small crystallites or low particle concentration. Concentration of the particles by centrifugation showed that in the large fraction (>20 nm), even less oxidized nanoparticles (46 wt % Cu and 54 wt % Cu2 O) were present, although the solubility of molecular oxygen is higher in acetone than in water. The nanoparticles in acetone were stable due to a Cu-catalyzed graphite layer formed on their surfaces. The influence of the solvent

  7. Enhancing the High Temperature Capability of Nanocrystalline Alloys: Utilizing Thermodynamic Stability Maps to Mitigate Grain Growth Through Solute Selection

    DTIC Science & Technology

    2013-12-01

    alloy contents. At higher solute concentrations x0, there is additional solute to stabilize the grain boundaries. At the higher Zr contents...element on grain boundary energy. The effect of ∆Hmix for Fe– Zr alloys is examined in figure 4 for x0 = 0.04 by systematically changing the ∆Hmix...values. For a hypothetical case of no chemical effect with ∆Hmix = 0, dm = 10 nm is predicted at the melting point of Fe. In an Fe–4% Zr alloy annealed at

  8. All-proportional solid-solution Rh-Pd-Pt alloy nanoparticles by femtosecond laser irradiation of aqueous solution with surfactant

    NASA Astrophysics Data System (ADS)

    Sarker, Md. Samiul Islam; Nakamura, Takahiro; Sato, Shunichi

    2015-06-01

    Formation of Rh-Pd-Pt solid-solution alloy nanoparticles (NPs) by femtosecond laser irradiation of aqueous solution in the presence of polyvinylpyrrolidone (PVP) or citrate as a stabilizer was studied. It was found that the addition of surfactant (PVP or citrate) significantly contributed to reduce the mean size of the particles to 3 nm for PVP and 10 nm for citrate, which was much smaller than that of the particles fabricated without any surfactants (20 nm), and improved the dispersion state as well as the colloidal stability. The solid-solution formation of the Rh-Pd-Pt alloy NPs was confirmed by the XRD results that the diffraction pattern was a single peak, which was found between the positions corresponding to each pure Rh, Pd, and Pt NPs. Moreover, all the elements were homogeneously distributed in every particle by STEM-EDS elemental mapping, strongly indicating the formation of homogeneous solid-solution alloy. Although the Rh-Pd-Pt alloy NPs fabricated with PVP was found to be Pt rich by EDS observation, the composition of NPs fabricated with citrate almost exactly preserved the feeding ratio of ions in the mixed solution. To our best knowledge, these results demonstrated for the first time, the formation of all-proportional solid-solution Rh-Pd-Pt alloy NPs with well size control.

  9. Improved accountability method for measuring enriched uranium in H-Canyon dissolver solution at the Savannah River Site

    SciTech Connect

    Maxwell, S.L. III; Satkowski, J.; Mahannah, R.N.

    1992-08-01

    At the Savannah River Site (SRS), accountability measurement of enriched uranium dissolved in H-Canyon is performed using isotope dilution mass spectrometry (IDMS). In the IDMS analytical method, a known quantity of uranium{sup 233} is added to the sample solution containing enriched uranium and fission products. The resulting uranium mixture must first be purified using a separation technique in the shielded analytical(``hot``) cells to lower radioactivity levels by removing fission products. Following this purification, the sample is analyzed by mass spectrometry to determine the total uranium content and isotopic abundance. The magnitude of the response of each uranium isotope in the sample solution and the response of the U{sup 233} spike is measured. By ratioing these responses, relative to the known quantity of the U{sup 233} spike, the uranium content can be determined. A hexane solvent extraction technique, used for years at SRS to remove fission products prior to the mass spectrometry analysis of uranium, has several problems. The hexone method is tedious, requires additional sample clean-up after the purified sample is removed from the shielded cells and requires the use of Resource Conservation and Recovery Act (RCRA)-listed hazardous materials (hexone and chromium compounds). A new high speed separation method that enables a rapid removal of fission products in a shielded cells environment has been developed by the SRS Central Laboratory to replace the hexone method. The new high speed column extraction chromatography technique employs applied vacuum and columns containing tri (2-ethyl-hexyl) phosphate (TEHP) solvent coated on a small particle inert support (SM-7 Bio Beads). The new separation is rapid, user friendly, eliminates the use of the RCA-listed hazardous chemicals and reduces the amount of solid waste generated by the separation method. 2 tabs. 4 figs.

  10. Improved accountability method for measuring enriched uranium in H-Canyon dissolver solution at the Savannah River Site

    SciTech Connect

    Maxwell, S.L. III; Satkowski, J.; Mahannah, R.N.

    1992-01-01

    At the Savannah River Site (SRS), accountability measurement of enriched uranium dissolved in H-Canyon is performed using isotope dilution mass spectrometry (IDMS). In the IDMS analytical method, a known quantity of uranium{sup 233} is added to the sample solution containing enriched uranium and fission products. The resulting uranium mixture must first be purified using a separation technique in the shielded analytical( hot'') cells to lower radioactivity levels by removing fission products. Following this purification, the sample is analyzed by mass spectrometry to determine the total uranium content and isotopic abundance. The magnitude of the response of each uranium isotope in the sample solution and the response of the U{sup 233} spike is measured. By ratioing these responses, relative to the known quantity of the U{sup 233} spike, the uranium content can be determined. A hexane solvent extraction technique, used for years at SRS to remove fission products prior to the mass spectrometry analysis of uranium, has several problems. The hexone method is tedious, requires additional sample clean-up after the purified sample is removed from the shielded cells and requires the use of Resource Conservation and Recovery Act (RCRA)-listed hazardous materials (hexone and chromium compounds). A new high speed separation method that enables a rapid removal of fission products in a shielded cells environment has been developed by the SRS Central Laboratory to replace the hexone method. The new high speed column extraction chromatography technique employs applied vacuum and columns containing tri (2-ethyl-hexyl) phosphate (TEHP) solvent coated on a small particle inert support (SM-7 Bio Beads). The new separation is rapid, user friendly, eliminates the use of the RCA-listed hazardous chemicals and reduces the amount of solid waste generated by the separation method. 2 tabs. 4 figs.

  11. Solution and diffusion of hydrogen isotopes in tungsten-rhenium alloy

    NASA Astrophysics Data System (ADS)

    Ren, Fei; Yin, Wen; Yu, Quanzhi; Jia, Xuejun; Zhao, Zongfang; Wang, Baotian

    2017-08-01

    Rhenium is one of the main transmutation elements forming in tungsten under neutron irradiation. Therefore, it is essential to understand the influence of rhenium impurity on hydrogen isotopes retention in tungsten. First-principle calculations were used to study the properties of hydrogen solution and diffusion in perfect tungsten-rhenium lattice. The interstitial hydrogen still prefers the tetrahedral site in presence of rhenium, and rhenium atom cannot act directly as a trapping site of hydrogen. The presence of rhenium in tungsten raises the solution energy and the real normal modes of vibration on the ground state and the transition state, compared to hydrogen in pure tungsten. Without zero point energy corrections, the presence of rhenium decreases slightly the migration barrier. It is found that although the solution energy would tend to increase slightly with the rising of the concentration of rhenium, but which does not influence noticeably the solution energy of hydrogen in tungsten-rhenium alloy. The solubility and diffusion coefficient of hydrogen in perfect tungsten and tungsten-rhenium alloy have been estimated, according to Sievert's law and harmonic transition state theory. The results show the solubility of hydrogen in tungsten agrees well the experimental data, and the presence of Re would decrease the solubility and increase the diffusivity for the perfect crystals.

  12. Stacking fault energies of face-centered cubic concentrated solid solution alloys

    DOE PAGES

    Zhao, Shijun; Stocks, G. Malcolm; Zhang, Yanwen

    2017-06-22

    We report the stacking fault energy (SFE) for a series of face-centered cubic (fcc) equiatomic concentrated solid solution alloys (CSAs) derived as subsystems from the NiCoFeCrMn and NiCoFeCrPd high entropy alloys based on ab initio calculations. At low temperatures, these CSAs display very low even negative SFEs, indicating that hexagonal close-pack (hcp) is more energy favorable than fcc structure. The temperature dependence of SFE for some CSAs is studied. With increasing temperature, a hcp-to-fcc transition is revealed for those CSAs with negative SFEs, which can be attributed to the role of intrinsic vibrational entropy. The analysis of the vibrational modesmore » suggests that the vibrational entropy arises from the high frequency states in the hcp structure that originate from local vibrational mode. Furthermore, our results underscore the importance of vibrational entropy in determining the temperature dependence of SFE for CSAs.« less

  13. Effects of Solution and Aging Treatments on Corrosion Resistance of As-cast 60NiTi Alloy

    NASA Astrophysics Data System (ADS)

    Qin, Qiuhui; Wen, Yuhua; Wang, Gaixia; Zhang, Lanhui

    2016-12-01

    60NiTi alloy has become a competitive candidate for bearing applications due to its shape memory effect, superelasticity, high strength, hardness, excellent abrasion resistance and corrosion resistance, etc. However, the relationship between its corrosion resistance and heat treatment is not clearly understood. Therefore, we used OM, XRD, SEM and EDS to study the evolution of microstructure in as-cast, solution-treated and aged 60NiTi alloy. Besides, the potentiodynamic polarization and salt spray test were used to compare corrosion resistance of 60NiTi alloy and 316 stainless steel and to study the effect of microstructures on corrosion resistance of 60NiTi alloy. The results show that the corrosion resistance of as-cast 60NiTi alloy is comparable to that of 316 stainless steel, but the corrosion resistance of solution-treated and aged 60NiTi alloys is much superior. The significantly reduced Ni3Ti phase after the solution and aging treatments is responsible for the remarkable improvement in the corrosion resistance of as-cast 60NiTi alloy.

  14. Study on Corrosion Performance of Cu-Te-Se Alloys in a 3.5% Sodium Chloride Solution

    NASA Astrophysics Data System (ADS)

    Jiao, Lin; Li, Meng; Zeng, Tao; Zhu, Dachuan

    2015-11-01

    Samples of Cu-Te-Se alloys, previously aged or treated as a solid solution, were immersed in 3.5% (mass fraction) sodium chloride solution to investigate their corrosion resistance at room temperature by determining their corrosive weight loss. The morphologies of the precipitated phase and surface products following immersion were observed by scanning electron microscope. In addition, energy-dispersive spectroscopic analysis was used to determine the elemental constituents of precipitated phase and corroded surface of the alloy samples. The phase composition was measured by x-ray diffraction, and the electrochemical polarization behavior of the samples was determined using an electrochemical workstation. The experimental results revealed that the alloy samples appeared to corrode uniformly, which was accompanied by a small amount of localized corrosion. There was the possibility that localized corrosion could increase following aging treatment. The addition of a small amount of tellurium and selenium to the alloy appeared to retard oxygen adsorption on the copper in the alloy, which has ameliorated the alloy corrosion due to the similar physical and chemical properties of oxygen. In comparison to the solid solution state, the corrosion resistance of the alloy appeared to decline slightly following aging treatment.

  15. [Corrosion of Ag-Pd-Cu alloys in saline solution. Amount of released elements and electrochemical corrosion].

    PubMed

    Kitaoka, M

    1989-03-01

    The effect of the Pd content on corrosion and tarnish resistance in twelve experimental alloys was investigated. The alloys were prepared with a composition of Pd content from 20.1 to 30.1 at %. The composition of the alloys Ag-20% Pd, Ag-25% Pd and Ag-30% Pd was varied by adding Cu 5 wt%, 10 wt% and 15 wt% to each of them. The corrosion resistance was estimated by the amount of the released Ag, Cu and by electrochemical corrosion behavior in 0.86% NaCl solution at 37 degrees C. The tarnish resistance was assessed using a spectrophotometer. The test solutions included 0.86% NaCl solution, 0.1% Na2S solution and a mixture of 1.0% lactic acid and 0.1% Na2S, all at 37 degrees C, in sealed containers. The results are summarized as follows. The larger the amount of Pd in Ag-Pd binary alloys and Ag-Pd-Cu ternary alloys, the more stable was the release and the release rate of Ag, Cu and corrosion resistance increased in 0.86% NaCl solution. The addition of Cu to Ag-Pd binary alloys increased the release and release rate of Ag, but there was a shift of the rest potential in the noble direction. A relationship was found between the amount of Ag and Cu released from Ag-Pd-Cu ternary alloys. In this study, an increase in corrosion resistance was observed when the content of Pd in Ag-Pd binary alloys was 25 wt%. Furthermore, it was also observed that Ag-Pd-Cu ternary alloys need an additional 30 wt% Pd for corrosion resistance. Moreover, the addition of Cu must be kept lower than 10 wt%. The tarnish resistance of the twelve experimental alloys was good in 0.86% NaCl solution but was barely improved with increased in the Pd content in sulfide solution. The correlation between electrochemical corrosion behavior and tarnish resistance was not significant, but the correlation between the amount of Ag, Cu release from Ag-Pd-Cu ternary alloys and tarnish resistance was remarkable.

  16. Microstructure, mechanical property and metal release of As-SLM CoCrW alloy under different solution treatment conditions.

    PubMed

    Lu, Yanjin; Wu, Songquan; Gan, Yiliang; Zhang, Shuyuan; Guo, Sai; Lin, Junjie; Lin, Jinxin

    2015-03-01

    In the study, the microstructure, mechanical property and metal release behavior of selective laser melted CoCrW alloys under different solution treatment conditions were systemically investigated to assess their potential use in orthopedic implants. The effects of the solution treatment on the microstructure, mechanical properties and metal release were systematically studied by OM, SEM, XRD, tensile test, and ICP-AES, respectively. The XRD indicated that during the solution treatment the alloy underwent the transformation of γ-fcc to ε-hcp phase; the ε-hcp phase nearly dominated in the alloy when treated at 1200°C following the water quenching; the results from OM, SEM showed that the microstructural change was occurred under different solution treatments; solution at 1150°C with furnace cooling contributed to the formation of larger precipitates at the grain boundary regions, while the size and number of the precipitates was decreased as heated above 1100°C with the water quenching; moreover, the diamond-like structure was invisible at higher solution temperature over 1150°C following water quenching; compared with the furnace cooling, the alloy quenched by water showed excellent mechanical properties and low amount of metal release; as the alloy heated at 1200°C, the mechanical properties of the alloy reached their optimum combination at UTS=1113.6MPa, 0.2%YS=639.5MPa, and E%=20.1%, whilst showed the lower total quantity of metal release. It is suggested that a proper solution treatment is an efficient strategy for improving the mechanical properties and corrosion resistance of As-SLM CoCrW alloy that show acceptable tensile ductility.

  17. Effect of carbon and alloying solute atoms on helium behaviors in α-Fe

    NASA Astrophysics Data System (ADS)

    Zhang, Yange; You, Yu-Wei; Xu, Yichun; Liu, C. S.; Chen, J. L.; Luo, G.-N.

    2017-02-01

    Helium bubbles could strongly degrade the mechanical properties of ferritic steels in fission and fusion systems. The formation of helium bubble is directly affected by the interactions between helium and the compositions in steels, such as solute atoms, carbon and irradiation defects. We thereby performed systematical first-principles calculations to investigate the interactions of solute-helium and carbon-solute-helium. It is found that substitutional helium is more attractive than interstitial helium to all the considered 3p, 4p, 5p and 6p solutes. The attraction between carbon and substitutional helium suggests the carbon-solute-helium complex can be formed stably. By examining the charge density difference and thermal stability, it is found that the ternary complex shows stronger attraction with He than that of solute-helium pair for some solutes (S, Se, In, Te, Pb and Bi) and the complex could existed in iron stably at 700 K. The present theoretical results may be helpful for exploring alloy additions to mitigate the formation of large helium bubbles.

  18. Magnetism and Solid Solution Effects in NiAI (40% AI) Alloys

    SciTech Connect

    Liu, Chain T; Fu, Chong Long; Chisholm, Matthew F; Thompson, James R; Krcmar, Maja; Wang, Xun-Li

    2007-01-01

    The solid solution effects of ternary additions of transition elements in intermetallic Ni-40% Al were investigated by both experimental studies and theoretical calculations. Co solute atoms when sitting at Ni sublattice sites do not affect the lattice parameter and hardening behavior of Ni-40Al. On the other hand, Fe, Mn, and Cr solutes, which are mainly on Al sublattice sites, substantially expand the lattice parameter and produce an unusual solid solution softening effect. First-principles calculations predict that these solute atoms with large unfilled d-band electrons develop large magnetic moments and effectively expand the lattice parameter when occupying Al sublattice sites. The theoretical predictions were verified by both electron loss-energy spectroscopy (EELS) analyses and magnetic susceptibility measurements. The observed softening behavior can be explained quantitatively by the replacement of Ni anti-site defects (potent hardeners) by Fe, Mn, and Cr anti-site defects with smaller atom size mismatch between solute and Al atoms. This study has led to the identification of magnetic interaction as an important physical parameter affecting the solid solution hardening in intermetallic alloys containing transition elements.

  19. Effects of Cooling Rate and Solute Content on the Grain Refinement of Mg-Gd-Y Alloys by Aluminum

    NASA Astrophysics Data System (ADS)

    Dai, Jichun; Easton, Mark A.; Zhang, Mingxing; Qiu, Dong; Xiong, Xiangyuan; Liu, Wencai; Wu, Guohua

    2014-09-01

    The effect of Al additions on grain refinement of Mg-Gd-Y alloys with different solute contents at different cooling rates has been investigated. For all alloys, significant grain refinement was due to the formation of Al2(Gd x Y1- x ) nucleant particles. The number density and size distribution of Al2(Gd x Y1- x ) were affected by both solute content and the cooling rate. Grain sizes ( d gs) of Mg-Gd-Y base alloys and of Mg-Gd-Y-Al alloys were related to solute content (defined by the growth restriction factor, Q), cooling rate (), and area number density ( ρ ns) and size ( d p) of nucleant particles that can be activated. It is found that grain sizes of Mg-Gd-Y base alloys follow the relationship , while grain sizes of Al-refined samples follow the relationship , where a, b, a', and b' were constants. In addition, the grain refinement effect of Al additions was more susceptible to solute content and the cooling rate than that of Zr which is regarded as the most efficient grain refiner for Mg alloys.

  20. Surface structure and electrochemical characteristics of Ti-V-Cr bcc-type solid solution alloys sintered with Ni

    SciTech Connect

    Tsuji, Yoichiro; Yamamoto, Osamu; Matsuda, Hiromu; Toyoguchi, Yoshinori

    2000-07-01

    Ti-V-Cr bcc-type solid solution alloys can absorb a large amount of hydrogen and be applied to active materials of the negative electrode in Ni-MH batteries. However, because of the insolubility of Ni into these alloys, the electrochemical characteristics like discharge capacity and cycle life were poor. In order to increase the discharge capacity of hydrogen absorbing alloy electrodes, Ti-V-Cr bcc-type alloy powders were sintered with Ni in order to form Ni contained surface layer on the alloy surface. As sintering temperature rose up, the surface composition changed from TiNi to Ti{sub 2}Ni. TiNi surface layer showed better electrochemical characteristics. For the Ni adding method, Ni electroless plating was preferred because of good adhesion. As a result of optimized conditions, a discharge capacity of 570 mAh/g and an improvement of cycle life were achieved.

  1. Phase-field modeling of binary alloy solidification with coupled heat and solute diffusion.

    PubMed

    Ramirez, J C; Beckermann, C; Karma, A; Diepers, H-J

    2004-05-01

    A phase-field model is developed for simulating quantitatively microstructural pattern formation in solidification of dilute binary alloys with coupled heat and solute diffusion. The model reduces to the sharp-interface equations in a computationally tractable thin-interface limit where (i). the width of the diffuse interface is about one order of magnitude smaller than the radius of curvature of the interface but much larger than the real microscopic width of a solid-liquid interface, and (ii). kinetic effects are negligible. A recently derived antitrapping current [Phys. Rev. Lett. 87, 115701 (2001)

  2. Extending cluster description to bimetallic nanowires: The ideal solid solution alloy case

    NASA Astrophysics Data System (ADS)

    Maras, E.; Braems, I.; Berthier, F.

    2011-12-01

    We present a comprehensive study of the equilibrium properties of two codeposited species for an alloy that forms an ideal solution, on a one-dimensional chain. By use of a cluster description we provide exact formulae of the coverages, the total density of clusters, the cluster size distribution, and the chemical composition of each cluster. These analytical results, that are proved to be in agreement with Monte Carlo simulations, strongly differ from the ones derived in the mean-field framework. Indeed, we show by depicting the codeposit at the macroscopic, mesoscopic, and atomic scales, that its features are to be related to the chemical heterogeneities at the edges of the clusters.

  3. Solid-solution CrCoCuFeNi high-entropy alloy thin films synthesized by sputter deposition

    DOE PAGES

    An, Zhinan; Jia, Haoling; Wu, Yueying; ...

    2015-05-04

    The concept of high configurational entropy requires that the high-entropy alloys (HEAs) yield single-phase solid solutions. However, phase separations are quite common in bulk HEAs. A five-element alloy, CrCoCuFeNi, was deposited via radio frequency magnetron sputtering and confirmed to be a single-phase solid solution through the high-energy synchrotron X-ray diffraction, energy-dispersive spectroscopy, wavelength-dispersive spectroscopy, and transmission electron microscopy. The formation of the solid-solution phase is presumed to be due to the high cooling rate of the sputter-deposition process.

  4. Corrosion behavior of titanium alloy Beta-21S coated with diamond like carbon in Hank's solution

    NASA Astrophysics Data System (ADS)

    Mohan, L.; Anandan, C.; Grips, V. K. William

    2012-06-01

    Diamond like carbon (DLC) coatings posses high hardness and low friction coefficient and also biocompatible, hence, they are of interest for enhancing the wear and corrosion resistance of bio-implant materials. Beta stabilized titanium alloys are attractive for biomedical applications because of their high specific strength and low modulus. In this work Beta-21S alloy (Ti-15Mo-3Nb-3Al-0.2Si) was implanted with carbon ions by plasma immersion ion implantation using methane and hydrogen gas mixture followed by DLC deposition by plasma enhanced chemical vapour deposition (PECVD). The implanted layers enabled deposition of adherent diamond-like carbon coatings on the titanium alloy which was otherwise not possible. The corrosion behavior of the treated and untreated samples was investigated through electrochemical impedance spectroscopy (EIS) and potentiodynamic polarization studies in simulated body fluid (Hank's solution). XPS, micro Raman and EDAX investigation of the samples showed the formation of a thin oxide layer on the treated samples after corrosion experiments. Corrosion resistance of the DLC coated sample is comparable with that of the untreated samples. Electrochemical impedance data of the substrate and implanted samples were fitted with two time constant equivalent circuits and that of DLC coated samples with two-layer model.

  5. Radiation-induced segregation on defect clusters in single-phase concentrated solid-solution alloys

    DOE PAGES

    Lu, Chenyang; Yang, Taini; Jin, Ke; ...

    2017-01-12

    A group of single-phase concentrated solid-solution alloys (SP-CSAs), including NiFe, NiCoFe, NiCoFeCr, as well as a high entropy alloy NiCoFeCrMn, was irradiated with 3 MeV Ni2+ ions at 773 K to a fluence of 5 1016 ions/cm2 for the study of radiation response with increasing compositional complexity. Advanced transmission electron microscopy (TEM) with electron energy loss spectroscopy (EELS) was used to characterize the dislocation loop distribution and radiation-induced segregation (RIS) on defect clusters in the SP-CSAs. The results show that a higher fraction of faulted loops exists in the more compositionally complex alloys, which indicate that increasing compositional complexity canmore » extend the incubation period and delay loop growth. The RIS behaviors of each element in the SP-CSAs were observed as follows: Ni and Co tend to enrich, but Cr, Fe and Mn prefer to deplete near the defect clusters. RIS level can be significantly suppressed by increasing compositional complexity due to the sluggish atom diffusion. According to molecular static (MS) simulations, disk like segregations may form near the faulted dislocation loops in the SP-CSAs. Segregated elements tend to distribute around the whole faulted loop as a disk rather than only around the edge of the loop.« less

  6. A solutal interaction mechanism for the columnar-to-equiaxed transition in alloy solidification

    NASA Astrophysics Data System (ADS)

    Martorano, M. A.; Beckermann, C.; Gandin, C.-A.

    2003-08-01

    A multiphase/multiscale model is used to predict the columnar-to-equiaxed transition (CET) during solidification of binary alloys. The model consists of averaged energy and species conservation equations, coupled with nucleation and growth laws for dendritic structures. A new mechanism for the CET is proposed based on solutal interactions between the equiaxed grains and the advancing columnar front—as opposed to the commonly used mechanical blocking criterion. The resulting differences in the CET prediction are demonstrated for cases where a steady state can be assumed, and a revised isotherm velocity (V T ) vs temperature gradient (G) map for the CET is presented. The model is validated by predicting the CET in previously performed unsteady, unidirectional solidification experiments involving Al-Si alloys of three different compositions. Good agreement is obtained between measured and predicted cooling curves. A parametric study is performed to investigate the dependence of the CET position on the nucleation undercooling and the density of nuclei in the equiaxed zone. Nucleation undercoolings are determined that provide the best agreement between measured and calculated CET positions. It is found that for all three alloy compositions, the nucleation undercoolings are very close to the maximum columnar dendrite tip undercoolings, indicating that the origin of the equiaxed grains may not be heterogeneous nucleation, but rather a breakdown or fragmentation of the columnar dendrites.

  7. Carbide Formation and Dissolution in Biomedical Co-Cr-Mo Alloys with Different Carbon Contents during Solution Treatment

    NASA Astrophysics Data System (ADS)

    Mineta, Shingo; Namba, Shigenobu; Yoneda, Takashi; Ueda, Kyosuke; Narushima, Takayuki

    2010-08-01

    The microstructures of as-cast and heat-treated biomedical Co-Cr-Mo (ASTM F75) alloys with four different carbon contents were investigated. The as-cast alloys were solution treated at 1473 to 1548 K for 0 to 43.2 ks. The precipitates in the matrix were electrolytically extracted from the as-cast and heat-treated alloys. An M23C6 type carbide and an intermetallic σ phase (Co(Cr,Mo)) were detected as precipitates in the as-cast Co-28Cr-6Mo-0.12C alloy; an M23C6 type carbide, a σ phase, an η phase (M6C-M12C type carbide), and a π phase (M2T3X type carbide with a β-manganese structure) were detected in the as-cast Co-28Cr-6Mo-0.15C alloy; and an M23C6 type carbide and an η phase were detected in the as-cast Co-28Cr-6Mo-0.25C and Co-28Cr-6Mo-0.35C alloys. After solution treatment, complete precipitate dissolution occurred in all four alloys. Under incomplete precipitate dissolution conditions, the phase and shape of precipitates depended on the heat-treatment conditions and the carbon content in the alloys. The π phase was detected in the alloys with carbon contents of 0.15, 0.25, and 0.35 mass pct after heat treatment at high temperature such as 1548 K for a short holding time of less than 1.8 ks. The presence of the π phase in the Co-Cr-Mo alloys has been revealed in this study for the first time.

  8. Removal of triazine-based pollutants from water by carbon nanotubes: Impact of dissolved organic matter (DOM) and solution chemistry.

    PubMed

    Engel, Maya; Chefetz, Benny

    2016-12-01

    Adsorption of organic pollutants by carbon nanotubes (CNTs) in the environment or removal of pollutants during water purification require deep understanding of the impacts of the presence of dissolved organic matter (DOM). DOM is an integral part of environmental systems and plays a key role affecting the behavior of organic pollutants. In this study, the effects of solution chemistry (pH and ionic strength) and the presence of DOM on the removal of atrazine and lamotrigine by single-walled CNTs (SWCNTs) was investigated. The solubility of atrazine slightly decreased (∼5%) in the presence of DOM, whereas that of lamotrigine was significantly enhanced (by up to ∼70%). Simultaneous introduction of DOM and pollutant resulted in suppression of removal of both atrazine and lamotrigine, which was attributed to DOM-pollutant competition or blockage of adsorption sites by DOM. However the decrease in removal of lamotrigine was also a result of its complexation with DOM. Pre-introduction of DOM significantly reduced pollutant adsorption by the SWCNTs, whereas introduction of DOM after the pollutant resulted in the release of adsorbed atrazine and lamotrigine from the SWCNTs. These data imply that DOM exhibits higher affinity for the adsorption sites than the triazine-based pollutants. In the absence of DOM atrazine was a more effective competitor than lamotrigine for adsorption sites in SWCNTs. However, competition between pollutants in the presence of DOM revealed lamotrigine as the better competitor. Our findings help unravel the complex DOM-organic pollutant-CNT system and will aid in CNT-implementation in water-purification technologies.

  9. Decreasing Bio-Degradation Rate of the Hydrothermal-Synthesizing Coated Mg Alloy via Pre-Solid-Solution Treatment

    PubMed Central

    Song, Dan; Li, Cheng; Zhang, Liwen; Ma, Xiaolong; Guo, Guanghui; Zhang, Fan; Jiang, Jinghua; Ma, Aibin

    2017-01-01

    In this study, we report an effective approach, pre-solid solution (SS) treatment, to reduce the in-vitro bio-degradation rate of the hydrothermal-synthesizing coated Mg–2Zn–Mn–Ca–Ce alloy in Hanks’ solution. Pre-SS treatment alters the microstructure of alloys, which benefits the corrosion resistances of the substrate itself and the formed coating as well. The micro-galvanic corrosion between the secondary phase (cathode) and the α-Mg phase (anode) is relieved due to the reduction of the secondary phase. Meanwhile, coating formed on the SS-treated alloy was compacter than that on as-cast alloy, which provides better protection against initial corrosion. PMID:28773223

  10. Effects of Oxidation Time on Micro-arc Oxidized Coatings of Magnesium Alloy AZ91D in Aluminate Solution

    NASA Astrophysics Data System (ADS)

    Mu, Weiyi; Li, Zhengxian; Du, Jihong; Luo, Ruixue; Xi, Zhengping

    Micro-arc oxidation coatings were prepared on magnesium alloy AZ91D at different oxidation times in aluminate solution. The effects of the oxidation time on the microstructure, growth rate and corrosion resistance of the coatings were investigated. The results indicate that the coatings are uniform in thickness and mainly composed of MgAl2O4 and MgO. There were many residual discharging channels on the coatings surface. The coatings improved the corrosion resistance of magnesium alloy AZ91D considerably. With increased oxidation time, the crystalline substances content and thickness of the coatings increased, while the growth rate of the coatings decreased, and the resulting coatings surface had lower porosity and larger pore sizes. In addition, the corrosion resistance of the coatings on magnesium alloy AZ91D surfaces is superior to the magnesium alloy AZ91D substrate in the NaCl solution, and the effect is more remarkable with longer oxidation times.

  11. Beyond temperature: Clumped isotope signatures in dissolved inorganic carbon species and the influence of solution chemistry on carbonate mineral composition

    USGS Publications Warehouse

    Tripati, Aradhna K.; Hill, Pamela S.; Eagle, Robert A.; Mosenfelder, Jed L.; Tang, Jianwu; Schauble, Edwin A.; Eiler, John M.; Zeebe, Richard E.; Uchikawa, Joji; Coplen, Tyler B.; Ries, Justin B.; Henry, Drew

    2015-01-01

    “Clumped-isotope” thermometry is an emerging tool to probe the temperature history of surface and subsurface environments based on measurements of the proportion of 13C and 18O isotopes bound to each other within carbonate minerals in 13C18O16O22- groups (heavy isotope “clumps”). Although most clumped isotope geothermometry implicitly presumes carbonate crystals have attained lattice equilibrium (i.e., thermodynamic equilibrium for a mineral, which is independent of solution chemistry), several factors other than temperature, including dissolved inorganic carbon (DIC) speciation may influence mineral isotopic signatures. Therefore we used a combination of approaches to understand the potential influence of different variables on the clumped isotope (and oxygen isotope) composition of minerals.We conducted witherite precipitation experiments at a single temperature and at varied pH to empirically determine 13C-18O bond ordering (Δ47) and δ18O of CO32- and HCO3- molecules at a 25 °C equilibrium. Ab initio cluster models based on density functional theory were used to predict equilibrium 13C-18O bond abundances and δ18O of different DIC species and minerals as a function of temperature. Experiments and theory indicate Δ47 and δ18O compositions of CO32- and HCO3- ions are significantly different from each other. Experiments constrain the Δ47-δ18O slope for a pH effect (0.011 ± 0.001; 12 ⩾ pH ⩾ 7). Rapidly-growing temperate corals exhibit disequilibrium mineral isotopic signatures with a Δ47-δ18O slope of 0.011 ± 0.003, consistent with a pH effect.Our theoretical calculations for carbonate minerals indicate equilibrium lattice calcite values for Δ47 and δ18O are intermediate between HCO3− and CO32−. We analyzed synthetic calcites grown at temperatures ranging from 0.5 to 50 °C with and without the enzyme carbonic anhydrase present. This enzyme catalyzes oxygen isotopic exchange between DIC species and is present in many

  12. Tree species related functional properties of dissolved and total organic matter in throughfall, stemflow and forest floor solutions

    NASA Astrophysics Data System (ADS)

    Michalzik, Beate; Bischoff, Sebastian; Schwarz, Martin; Siemens, Jan; Thieme, Lisa; Wilcke, Wolfgang

    2016-04-01

    The amount and chemical nature of water-bound organic matter is a prerequisite for advancing our understanding of the C and nutrient cycling and associated ecosystem processes. While many investigations have addressed the nature and dynamics of DOM in terrestrial ecosystems, only a few have investigated the dynamics and composition of water-bound total OM (TOM) including the particulate organic matter fraction (POM; 0.45 μm < POM < 500 μm). Since water-bound element and nutrient concentrations are conventionally measured after 0.45 μm-filtration, the exclusion of the POM fraction results in misleading inferences and budgeting gaps of nutrient and energy fluxes in terrestrial ecosystems. Furthermore, tree species differ in leaf composition (e.g. nutrient, polyphenols content) and leaf litter quality, which in turn affect a variety of ecosystem processes. Nevertheless, the composition and amount of DOM and TOM derived from living plant material via throughfall (TF), stemflow (SF) and its compositional fate traversing the forest floor (FF) are insufficiently understood. In particular we asked: How do tree species and forest types affect the amount of dissolved and particulate C and N in TF and FF solutions and thus the input into the mineral soil? Do functional properties (e.g. aromaticity) of DOM and TOM differ in TF, SF and FF solutions collected in beech and spruce stands and among different beech stands across Germany? To monitor (mineral) soil input fluxes of DOM and POM in different spruce and beech forests, we fortnightly sampled TF and FF solution over three years (2010-2012) in the "Hainich-Dün-Exploratory", Thuringia, Central Germany, which forms part of the DFG SPP 1374 "Exploratories for Large-scale and Long-term Functional Biodiversity Research". To characterize chemical properties of DOM and TOM, we applied solid-state 13C NMR spectroscopy to TF, SF and FF solutions from three European beech regions across Germany and from Norway spruce sites of the

  13. Beyond temperature: Clumped isotope signatures in dissolved inorganic carbon species and the influence of solution chemistry on carbonate mineral composition

    NASA Astrophysics Data System (ADS)

    Tripati, Aradhna K.; Hill, Pamela S.; Eagle, Robert A.; Mosenfelder, Jed L.; Tang, Jianwu; Schauble, Edwin A.; Eiler, John M.; Zeebe, Richard E.; Uchikawa, Joji; Coplen, Tyler B.; Ries, Justin B.; Henry, Drew

    2015-10-01

    "Clumped-isotope" thermometry is an emerging tool to probe the temperature history of surface and subsurface environments based on measurements of the proportion of 13C and 18O isotopes bound to each other within carbonate minerals in 13C18O16O22- groups (heavy isotope "clumps"). Although most clumped isotope geothermometry implicitly presumes carbonate crystals have attained lattice equilibrium (i.e., thermodynamic equilibrium for a mineral, which is independent of solution chemistry), several factors other than temperature, including dissolved inorganic carbon (DIC) speciation may influence mineral isotopic signatures. Therefore we used a combination of approaches to understand the potential influence of different variables on the clumped isotope (and oxygen isotope) composition of minerals. We conducted witherite precipitation experiments at a single temperature and at varied pH to empirically determine 13C-18O bond ordering (Δ47) and δ18O of CO32- and HCO3- molecules at a 25 °C equilibrium. Ab initio cluster models based on density functional theory were used to predict equilibrium 13C-18O bond abundances and δ18O of different DIC species and minerals as a function of temperature. Experiments and theory indicate Δ47 and δ18O compositions of CO32- and HCO3- ions are significantly different from each other. Experiments constrain the Δ47-δ18O slope for a pH effect (0.011 ± 0.001; 12 ⩾ pH ⩾ 7). Rapidly-growing temperate corals exhibit disequilibrium mineral isotopic signatures with a Δ47-δ18O slope of 0.011 ± 0.003, consistent with a pH effect. Our theoretical calculations for carbonate minerals indicate equilibrium lattice calcite values for Δ47 and δ18O are intermediate between HCO3- and CO32-. We analyzed synthetic calcites grown at temperatures ranging from 0.5 to 50 °C with and without the enzyme carbonic anhydrase present. This enzyme catalyzes oxygen isotopic exchange between DIC species and is present in many natural systems. The two

  14. Corrosion of uranium and its low content Zr, Nb, and Ru alloys in aqueous solutions

    SciTech Connect

    Peretrukhin, V. F.; Maslennikov, Alexander; Tsivadze, A. Y.; Delegard, Calvin H.; Yusov, A. B.; Shilov, V. P.; Bessonov, A. A.; German, Konstantin E.; Fedosseev, A. M.; Kazanskii, L. P.; Budanova, Natalya; Kareta, A. V.; Gogolev, A. V.; Gedgovd, K.; Bulatov, G. S.

    2008-06-19

    Corrosion of uranium and its alloys with low content (0.5-5.0 at %) of Zr, Nb, and Ru in water and bicarbonate aqueous solutions is studied; the effect of hydrogen peroxide, the main product of radiation processes, on the corrosion rate is elucidated. The rate of the primary corrosion process is measured by electrochemical methods in anaerobic and aerobic conditions for uranium metal and its alloys containing 0.5 to 5.0 at % of Zr, Nb, and Ru. It is shown that the corrosion rates for the alloys are lower than that of reactor-grade uranium; however, the difference is rather close to the measurement error. The corrosion mechanism is studied; U(III) is shown to be rather unstable in neutral solutions when uranium(III) hydroxide is precipitated and no significant amount of U(III) and UH3 is present among the products of the metallic uranium corrosion in water. The kinetics of the second corrosion stage U(IV) + O2 -> U(VI) is studied by spectrophotometric method. It is shown that the reaction of U(IV) oxidation by atmospheric oxygen is similar in weakly acid solutions (pH 1.5-4.0) and in bicarbonate media: in particular, it has an induction period for uranium (IV) accumulation, after which the reaction accelerates; it is formally a first-order reaction with respect to uranium. The reaction mechanisms differ in the two media: in weakly acid solutions, after the appearance of U(VI), the reproportionation reaction proceeds; thus formed U(V) interacts with O2 faster than U(IV). In the bicarbonate medium, the acceleration of the reaction is due to the formation of a [U(IV)-U(VI)] complex whose reactivity is higher than that of uranium (IV). In the absence of bicarbonate, of great importance is the formation of a copolymer of U(IV) and U(VI), which at pH≥4 prevents formation of U(V). It is shown that on the introduction of hydrogen peroxide to aqueous solutions, the metallic uranium surface becomes transpassive, which increases the rate of corrosion process by at least an

  15. Environment-assisted cracking of Fe-32% Mn-9% Al alloys in 3.5% sodium chloride solution

    SciTech Connect

    Chang, S.C.; Liu, J.Y.; Juang, H.K.

    1995-05-01

    The stress corrosion cracking (SCC) behavior of four austenitic Fe-32% Mn-9% Al alloys containing {approx} 1 wt% carbon was studied. All of the four alloys were susceptible to SCC in room temperature and 160 C NaCl solution. SCC was enhanced by applying an anodic potential. The crack path was transgranular, and cleavage-like regions were observed on the fracture surface. The corrosion-assisted microcleavage model proposed for the transgranular SCC behavior of face-centered cubic (fcc) materials very likely was the operating SCC mechanism of the austenitic Fe-Mn-Al alloys. Adding 1.23% Mo or 1.27% Si to the austenitic Fe-32% Mn-9% Al alloys did not change the SCC mechanism and crack paths. Adding 1.27% Si made the alloys more susceptible to SCC, but no such effect was observed with the addition of 1.23% Mo. All four alloys studied were susceptible to hydrogen embrittlement (HE) in 3.5% NaCl solution at large cathodic applied potentials, and the crack paths were intergranular. The addition of Mo, Cr, or Si in the alloy displaced the potential at which HE occurred to more cathodic values.

  16. The evolution of the deformation substructure in a Ni-Co-Cr equiatomic solid solution alloy

    DOE PAGES

    Miao, Jiashi; Slone, C. E.; Smith, T. M.; ...

    2017-05-15

    The equiatomic NiCoCr alloy exhibits an excellent combination of strength and ductility, even greater than the FeNiCrCoMn high entropy alloy, and also displays a simultaneous increase in strength and ductility with decreasing the testing temperature. To systemically investigate the origin of the exceptional properties of NiCoCr alloy, which are related to the evolution of the deformation substructure with strain, interrupted tensile testing was conducted on the equiatomic NiCoCr single-phase solid solution alloy at both cryogenic and room temperatures at five different plastic strain levels of 1.5%, 6.5%, 29%, 50% and 70%. The evolution of deformation substructure was examined using electronmore » backscatter diffraction (EBSD), transmission Kikuchi diffraction (TKD), conventional transmission electron microscopy (CTEM), diffraction contrast imaging using STEM (DCI-STEM) and atomic resolution scanning transmission electron microscopy. While the deformation substructure mainly consisted of planar dislocation slip and the dissociation of dislocations into stacking faults at small strain levels (≤6.5%), at larger strain levels, additional substructures including nanotwins and a new phase with hexagonal close packed (HCP) lamellae also appeared. The volume fraction of the HCP lamellae increases with increasing deformation, especially at cryogenic temperature. First principles calculations at 0 K indicate that the HCP phase is indeed energetically favorable relative to FCC for this composition. In conclusion, the effects of the nanotwin and HCP lamellar structures on hardening rate and ductility at both cryogenic and room temperature are qualitatively discussed.« less

  17. The stability of DLC film on nitrided CoCrMo alloy in phosphate buffer solution

    NASA Astrophysics Data System (ADS)

    Zhang, T. F.; Liu, B.; Wu, B. J.; Liu, J.; Sun, H.; Leng, Y. X.; Huang, N.

    2014-07-01

    CoCrMo alloy is often used as the material for metal artificial joint, but metal debris and metal ions are the main concern on tissue inflammation or tissue proliferation for metal prosthesis. In this paper, nitrogen ion implantation and diamond like carbon (DLC) film composite treatment was used to reduce the wear and ion release of biomedical CoCrMo substrate. The mechanical properties and stability of N-implanted/DLC composite layer in phosphate buffer solution (PBS) was evaluated to explore the full potential of N-implanted/DLC composite layer as an artificial joint surface modification material. The results showed that the DLC film on N implanted CoCrMo (N-implanted/DLC composite layer) had the higher surface hardness and wear resistance than the DLC film on virgin CoCrMo alloy, which was resulted from the strengthen effect of the N implanted layer on CoCrMo alloy. After 30 days immersion in PBS, the structure of DLC film on virgin CoCrMo or on N implanted CoCrMo had no visible change. But the adhesion and corrosion resistance of DLC on N implanted CoCrMo (N-implanted/DLC composite layer) was weakened due to the dissolution of the N implanted layer after 30 days immersion in PBS. The adhesion reduction of N-implanted/DLC composite layer was adverse for in vivo application in long term. So researcher should be cautious to use N implanted layer as an inter-layer for increasing CoCrMo alloy load carrying capacity in vivo environment.

  18. Electrochemical and surface analyses of nanostructured Ti-24Nb-4Zr-8Sn alloys in simulated body solution.

    PubMed

    Li, J; Li, S J; Hao, Y L; Huang, H H; Bai, Y; Hao, Y Q; Guo, Z; Xue, J Q; Yang, R

    2014-06-01

    The use of nanostructuring to improve the stability of passive thin films on biomaterials can enhance their effectiveness in corrosion resistance and reduce the release of ions. The thickness of the ultrathin films that cover Ti and Ti alloys (only several nanometers) has prevented researchers from establishing systematic methods for their characterization. This study employed a multifunctional biomedical titanium alloy Ti-24Nb-4Zr-8Sn (wt.%) as a model material. Coarse-grained (CG) and nanostructured (NS) alloys were analyzed in 0.9% NaCl solution at 37°C. To reveal the details of the passive film, a method of sample preparation producing a passive layer suitable for transmission electron microscope analysis was developed. Electrochemical corrosion behavior was evaluated by potentiodynamic polarization tests and Mott-Schottky measurements. Surface depth chemical profile and morphology evolution were performed by X-ray photoelectron spectroscopy and in situ atomic force microscopy, respectively. A mechanism was proposed on the basis of the point defect model to compare the corrosion resistance of the passive film on NS and CG alloys. Results showed that the protective amorphous film on NS alloy is thicker, denser and more homogeneous with fewer defects than that on CG alloy. The film on NS alloy contains more oxygen and corrosion-resistant elements (Ti and Nb), as well as their suboxides, compared with the film on CG alloy. These characteristics can be attributed to the rapid, uniform growth of the passive film facilitated by nanostructuring.

  19. Effect of dysprosium on the kinetics and structural transformations during the decomposition of the supersaturated solid solution in magnesium-samarium alloys

    NASA Astrophysics Data System (ADS)

    Rokhlin, L. L.; Luk'yanova, E. A.; Tabachkova, N. Yu.; Dobatkina, T. V.; Tarytina, I. E.; Korol'kova, I. G.

    2017-03-01

    The effect of dysprosium added in the amounts such that it does not form an individual phase in equilibrium with solid magnesium on the decomposition of the supersaturated magnesium solid solution in Mg-Sm alloys is studied. The presence of dysprosium in Mg-Sm alloys is found to retard the decomposition of the supersaturated magnesium solid solution and to increase the hardening effect upon aging. When these alloys are aged, dysprosium is partly retained in the magnesium solid solution and partly enters into the compositions of the phases that form during the decomposition of the solid solution and are characteristic of Mg-Sm alloys.

  20. The Influence of the Effect of Solute on the Thermodynamic Driving Force on Grain Refinement of Al Alloys

    NASA Astrophysics Data System (ADS)

    Wang, Feng; Liu, Zhi-Lin; Qiu, Dong; Taylor, John A.; Easton, Mark A.; Zhang, Ming-Xing

    2015-01-01

    Grain refinement is known to be strongly affected by the solute in cast alloys. Addition of some solute can reduce grain size considerably while others have a limited effect. This is usually attributed to the constitutional supercooling which is quantified by the growth restriction factor, Q. However, one factor that has not been considered is whether different solutes have differing effects on the thermodynamic driving force for solidification. This paper reveals that addition of solute reduces the driving force for solidification for a given undercooling, and that for a particular Q value, it is reduced more substantially when adding eutectic-forming solutes than peritectic-forming elements. Therefore, compared with the eutectic-forming solutes, addition of peritectic-forming solutes into Al alloys not only possesses a higher initial nucleation rate resulted from the larger thermodynamic driving force for solidification, but also promotes nucleation within the constitutionally supercooled zone during growth. As subsequent nucleation can occur at smaller constitutional supercoolings for peritectic-forming elements, a smaller grain size is thus produced. The very small constitutional supercooling required to trigger subsequent nucleation in alloys containing Ti is considered as a major contributor to its extraordinary grain refining efficiency in cast Al alloys even without the deliberate addition of inoculants.

  1. Adsorption of Pb and Zn from binary metal solutions and in the presence of dissolved organic carbon by DTPA-functionalised, silica-coated magnetic nanoparticles.

    PubMed

    Hughes, D L; Afsar, A; Harwood, L M; Jiang, T; Laventine, D M; Shaw, L J; Hodson, M E

    2017-09-01

    The ability of diethylenetriaminepentaacetic acid (DTPA)-functionalised, silica-coated magnetic nanoparticles to adsorb Pb and Zn from single and bi-metallic metal solutions and from solutions containing dissolved organic carbon was assessed. In all experiments 10 mL solutions containing 10 mg of nanoparticles were used. For single metal solutions (10 mg L(-1) Pb or Zn) at pH 2 to 8, extraction efficiencies were typically >70%. In bi-metallic experiments, examining the effect of a background of either Zn or Pb (0.025 mmol L(-1)) on the adsorption of variable concentrations (0-0.045 mmol L(-1)) of the other metal (Pb or Zn, respectively) adsorption was well modelled by linear isotherms (R(2) > 0.60; p ≤ 0.001) and Pb was preferentially adsorbed relative to Zn. In dissolved organic carbon experiments, the presence of fulvic acid (0, 2.1 and 21 mg DOC L(-1)) reduced Pb and Zn adsorption from 0.01, 0.1 and 1.0 mmol L(-1) solutions. However, even at 21 mg DOC L(-1) fulvic acid, extraction efficiencies from 0.01 to 0.1 mmol L(-1) solutions remained >80% (Pb) and >50% (Zn). Decreases in extraction efficiency were significant between initial metal concentrations of 0.1 and 1.0 mmol L(-1) indicating that at metal loadings between c. 100 mg kg(-1) and 300 mg kg(-1) occupancy of adsorption sites began to limit further adsorption. The nanoparticles have the potential to perform effectively as metal adsorbents in systems containing more than one metal and dissolved organic carbon at a range of pH values. Copyright © 2017. Published by Elsevier Ltd.

  2. Local structures and the dissolving behavior of aqueous ammonia and its KCl and NH4Cl solutions: A Raman spectroscopy and X-ray scattering study

    NASA Astrophysics Data System (ADS)

    Li, Shenyu; Yuan, Junsheng; Li, Fei; Liu, Ziyu

    2016-06-01

    The aqueous ammonia (5%-15%) and its KCl and NH4Cl solutions have been studied by Raman spectroscopy and X-ray scattering. The microscopic structures in these solutions were proposed. The addition of KCl reinforced the hydrogen bond between NH3 and H2O. On contrary, NH4Cl destroyed this interaction by forming hydrogen bond NH4+-NH3. This study gave an interpretation of the different dissolving behavior of KCl and NH4Cl in aqueous ammonia, which may have important implications in the separation of potassium and ammonium salt during the industrial production.

  3. Effect of gelatin additive on microstructure and composition of electrodeposited rhenium-nickel alloys in aqueous solutions

    NASA Astrophysics Data System (ADS)

    Wu, Wangping

    2016-12-01

    Re-Ni alloys with high Re content were electrodeposited galvanostatically from aqueous solutions with addition of gelatin. The influence of gelatin on the Faradaic efficiency (FE), chemical composition, morphology and crystallographic structure of the alloys was investigated. Morphology, surface roughness, chemical composition and phase identification of the alloys were characterized by an environmental scanning electron microscopy, atomic force microscopy, energy-dispersive spectroscopy and X-ray diffraction, respectively. The addition of gelatin in the plating led to the increase in Re content, and the decrease in the FE and deposition rate. In the absence and presence of gelatin, the alloys with high Re content consisted of an amorphous phase. The addition of gelatin resulted in small amount of carbon in the alloys due to the adsorption of gelatin in the alloy. The gelatin had a great influence on the morphology of the alloys, resulting in significant grain coarsening, the increase in surface roughness and the decrease in crack size. The optimum concentration of gelatin was found to be about 0.9-2.7 g L-1.

  4. Study of solid-solution hardening in binary aluminium-based alloys

    NASA Astrophysics Data System (ADS)

    Draissia, Mohamed; Debili, Mohamed-Yacine

    2005-09-01

    Solid-solution formation in binary aluminium-based alloys is due essentially to the combined effects of the size and valence of solvent and solute atoms, as expected by the four Hume-Rothery rules. The lattice parameter of aluminium in the solid solution of the sputtered Al-Fe films is [Al-a (Å)=4.052-6.6×10-3Y]. The increasing and decreasing evolution of the lattice parameter of copper [Cu-a (Å)=3.612+1.8×10-3Z] and aluminium [Al-a (Å)=4.048-1.6×10-3X] in the sputtered Al-1.8 to 92.5 at. % Cu films is a result of the difference in size between the aluminium and copper atoms. The low solubility of copper in aluminium (<1.8 at % Cu) is due to the valences of solvent and solute atoms in contrast with other sputtered films prepared under similar conditions, such as Al-Mg (20 at. % Mg), Al-Ti (27 at. % Ti), Al-Cr (5at. % Cr) and Al-Fe (5.5 at. % Fe) where the solubility is due to the difference in size.

  5. Characterization of the chemical conversion films that form on Mg-Al alloy in colloidal silica solution

    NASA Astrophysics Data System (ADS)

    Kim, Seong-Jong; Zhou, Ying; Ichino, Ryoichi; Okido, Masazumi; Tanikawa, Shoji

    2003-04-01

    Chemical conversion treatment of Mg-Al alloy (AZ91) using colloidal silica as an alternative to chromate conversion was investigated as a function of solution pH, temperature, solution conditions, and treatment time. The solution used for the colloidal silica coating consisted of colloidal silica, titanium sulfate, and cobalt ions to maintain good anti-corrosion and adhesion properties. Adding CoSO4 to the colloidal silica solution enhanced the adhesion force between the silica film and magnesium substrate. The optimum conditions for the chemical conversion treatment solution were pH 2, 90-sec treatment, and 25°C.

  6. Computer simulation of the motion of a straight dislocation line in concentrated solid solutions. II. [in fcc alloys

    NASA Technical Reports Server (NTRS)

    Kuo, C. T. K.; Arsenault, R. J.

    1977-01-01

    An investigation was undertaken to determine if the size and modulus interaction of a solute atom with a screw dislocation and the modulus interaction with an edge dislocation contributed to strengthening, in addition to the size interaction with an edge dislocation. The results indicate that the size interaction between solute atom and an edge dislocation accounts for most of the solid solution strengthening in f.c.c. alloys. The contribution to the yield stress from the modulus interaction with an edge dislocation is less than 15%. The interaction between a solute atom and a screw dislocation is much less than that between a solute atom and an edge dislocation.

  7. The complex action of major solutes on radiation induced swelling of Fe-Cr-Ni austenitic alloys

    SciTech Connect

    Garner, F.A. ); Lauritzen, T. ); Mitchell, M.A. )

    1992-06-01

    The radiation-induced swelling of simple Fe-Cr-Ni austenitic alloys is sensitive to solute additions. It is shown in this paper that three of the most common solute elements (P,Si,Mo) exert a very complex and often non-monotonic influence on swelling with increasing solute level. The complexity of this influence and its dependence on other variables appears to be the result of a closely balanced competition between two or more roles played by each solute in its interaction with both vacancies and interstitials. This competition yields a variety of different swelling behaviors in response to changes in solute or solvent composition, displacement rate, and irradiation temperature.

  8. Final Report for the Study on S-Implanted Alloy 22 in 1 M NaCl Solutions

    SciTech Connect

    Windisch, Charles F.; Baer, Donald R.; Jones, R. H.; Engelhard, Mark H.

    2005-11-01

    The objective of this study was to examine the effects of high levels of S in the near-surface region on the passivity of Alloy 22, a corrosion resistant Ni-Cr-Mo alloy, in deaerated 1 M NaCl solution. Near-surface concentrations of S up to 2 at.% were achieved in Alloy 22 test specimens by implanting them with S. The S-implanted samples were then evaluated in short-term electrochemical tests in the salt solution and subsequently analyzed with X-ray Photoelectron Spectroscopy (XPS) for film thickness and composition. Specimens tested included non-implanted and annealed Alloy 22 samples, samples implanted with S, and “blanks” implanted with Ar as an ion that would simulate the “damage” of S implantation without the chemical effect. A sample of S-implanted Alloy 22 was also exposed to solution for 29 days and analyzed for evidence of S accumulation at the surface over longer times.

  9. Enhanced electrochemical degradation of ibuprofen in aqueous solution by PtRu alloy catalyst.

    PubMed

    Chang, Chiung-Fen; Chen, Tsan-Yao; Chin, Ching-Ju Monica; Kuo, Yu-Tsun

    2017-05-01

    Electrochemical advanced oxidation processes (EAOPs) regarded as a green technology for aqueous ibuprofen treatment was investigated in this study. Multi-walled carbon nanotubes (MWCNTs), Pt nanoparticles (Pt NPs), and PtRu alloy, of which physicochemical properties were characterized by XRD and X-ray absorption spectroscopy, were used to synthesize three types of cheap and effective anodes based on commercial conductive glass. Furthermore, the operating parameters, such as the current densities, initial concentrations, and solution pH were also investigated. The intermediates determined by a UPLC-Q-TOF/MS system were used to evaluate the possible reaction pathway of ibuprofen (IBU). The results revealed that the usage of MWCNTs and PtRu alloy can effectively reduce the grain size of electrocatalysts and increase the surface activity from the XRD and XANES analysis. The results of CV analysis, degradation and mineralization efficiencies revealed that the EAOPs with PtRu-FTO anode were very effective due to advantages of the higher capacitance, CO tolerance, catalytic ability at less positive voltage and stability. The concentration trend of intermediates indicated that the potential cytotoxic to human caused by 1-(1-hydroxyenthyl)-4-isobutylbenzene was completely eliminated as the reaction time reaches 60 min. Therefore, EAOPs combined with synthesized anodes can be feasibly applied on the electrochemical degradation of ibuprofen. Copyright © 2017 Elsevier Ltd. All rights reserved.

  10. Two-dimensional solid solution alloy of Bi-Pb binary films on Rh(111)

    NASA Astrophysics Data System (ADS)

    Yuhara, J.; Yokoyama, M.; Matsui, T.

    2011-10-01

    We studied the atomic arrangements and phase diagrams of two-dimensional (2D) Bi-Pb binary films on a Rh(111) surface with low-energy electron diffraction (LEED), scanning tunneling microscopy (STM), and Auger electron spectroscopy. The 2D binary films exhibited incommensurate (4 × 4) LEED patterns with any compositional ratio of Bi:Pb. Atomically resolved STM images revealed that the binary films formed hexagonal, close-packed structures in a 2D solid solution alloy. We found that the 2D binary films followed the Hume-Rothery rule. The interatomic distance decreased linearly from 0.359 nm to 0.342 nm with increasing proportions of Pb. This indicated that the lattice constant of the 2D binary films followed Vegard's law.

  11. Corrosion Performance of Fe-Cr-Ni Alloys in Artificial Saliva and Mouthwash Solution

    PubMed Central

    Porcayo-Calderon, J.; Casales-Diaz, M.; Salinas-Bravo, V. M.; Martinez-Gomez, L.

    2015-01-01

    Several austenitic stainless steels suitable for high temperature applications because of their high corrosion resistance and excellent mechanical properties were investigated as biomaterials for dental use. The steels were evaluated by electrochemical techniques such as potentiodynamic polarization curves, cyclic polarization curves, measurements of open circuit potential, and linear polarization resistance. The performance of steels was evaluated in two types of environments: artificial saliva and mouthwash solution at 37°C for 48 hours. In order to compare the behavior of steels, titanium a material commonly used in dental applications was also tested in the same conditions. Results show that tested steels have characteristics that may make them attractive as biomaterials for dental applications. Contents of Cr, Ni, and other minor alloying elements (Mo, Ti, and Nb) determine the performance of stainless steels. In artificial saliva steels show a corrosion rate of the same order of magnitude as titanium and in mouthwash have greater corrosion resistance than titanium. PMID:26064083

  12. Effects of pH, dissolved oxygen, and ionic strength on the survival of Escherichia coli O157:H7 in organic acid solutions.

    PubMed

    Kreske, Audrey C; Bjornsdottir, Kristin; Breidt, Fred; Hassan, Hosni

    2008-12-01

    The ability of Escherichia coli O157:H7 to survive in acidified vegetable products is of concern because of previously documented outbreaks associated with fruit juices. A study was conducted to determine the survival of E. coli O157:H7 in organic acids at pH values typical of acidified vegetable products (pH 3.2 and 3.7) under different dissolved oxygen conditions (< or = 0.05 and 5 mg/liter) and a range of ionic strengths (0.086 to 1.14). All solutions contained 20 mM gluconic acid, which was used as a noninhibitory low pH buffer to compare the individual acid effect to that of pH alone on the survival of E. coli O157:H7. E. coli O157:H7 cells challenged in buffered solution with ca. 5-mg/liter dissolved oxygen (present in tap water) over a range of ionic strengths at pH 3.2 exhibited a decrease in survival over 6 h at 30 degrees C as the ionic strength was increased. Cells challenged in 40 mM protonated L-lactic and acetic acid solutions with ionic strength of 0.684 achieved a > 4.7-log CFU/ml reduction at pH 3.2. However, under oxygen-limiting conditions in an anaerobic chamber, with < or = 0.05-mg/ liter oxygen, E. coli O157:H7 cells showed < or = 1.55-log CFU/ml reduction regardless of pH, acid type, concentration, or ionic strength. Many acid and acidified foods are sold in hermetically sealed containers with oxygen-limiting conditions. Our results demonstrate that E. coli O157:H7 may survive better than previously expected from studies with acid solutions containing dissolved oxygen.

  13. The Electrochemical Behavior of Zn-Mn Alloy Coating in Carbonated Concrete Solution

    NASA Astrophysics Data System (ADS)

    Touazi, S.; Bučko, M.; Makhloufi, L.; Legat, A.; Bajat, J. B.

    2016-05-01

    In order to improve the protective performance of Zn coating on reinforcing steel in concrete, the electrochemical deposition of Zn-Mn coatings was conducted on steel surface. The morphology, chemical and phase compositions of Zn-Mn coatings obtained from sulfate-citrate bath were investigated in the first part of paper. In the second part, the obtained deposits were tested in solution simulating carbonated concrete, consisting of NaHCO3 and Na2CO3. Data obtained from Tafel analysis showed higher corrosion resistance for Zn-Mn alloy deposits obtained at -1700 and -1800mV versus SCE, when compared to pure Zn deposit. Impedance spectroscopy investigations revealed that the total impedance of Zn-Mn coatings increased steadily with time, and was significantly higher as compared to pure Zn after 24h in corrosion solution. On the contrary, for pure Zn, the impedance increased in the first 12h, and then decreased during prolonged exposure time, which can be explained by rapid growth of nonprotective white rust and the degradation of zinc coating, as was confirmed by optical microscope after 24h of immersion in carbonated concrete pore solution.

  14. A New Thermodynamic Parameter to Predict Formation of Solid Solution or Intermetallic Phases in High Entropy Alloys (Postprint)

    DTIC Science & Technology

    2015-11-02

    AFRL-RX-WP-JA-2016-0345 A NEW THERMODYNAMIC PARAMETER TO PREDICT FORMATION OF SOLID SOLUTION OR INTERMETALLIC PHASES IN HIGH ENTROPY...Interim 22 September 2014 – 21 September 2015 4. TITLE AND SUBTITLE A NEW THERMODYNAMIC PARAMETER TO PREDICT FORMATION OF SOLID SOLUTION OR...simple thermodynamic criterion is proposed to predict the presence or absence of equilibrium intermetallic phases in a high entropy alloy at a given

  15. Thermal expansion and transformation behavior of cerium and plutonium alloys: an application of the Aptekar-Ponyatovsky regular solution model.

    PubMed

    Lawson, A C; Lashley, J C

    2011-09-14

    In this paper we apply the Aptekar-Ponyatovsky (AP) regular solution thermodynamic model to the analysis of experimental data for the coefficient of thermal expansion (CTE) and determine the AP model parameters for unalloyed cerium metal, Ce-Th-La alloys, and Pu-Ga alloys. We find that the high temperature CTE of cerium metal follows the predictions of the AP model based on low temperature, high pressure data. For Ce-Th-La alloys we use the AP parameters to track the suppression of the first-order γ-α cerium transition. We show the AP model accounts for the negative CTE observed for Pu-Ga alloys and is equivalent to an earlier invar model. Finally, we apply the AP parameters obtained for Pu-Ga alloys to rationalize the observed δ-α transformation pressures of these alloys. We show that the anomalous values of the Grüneisen and Grüneisen-Anderson parameters are important features of the thermal properties of plutonium. A strong analogy between the properties of plutonium and cerium is confirmed.

  16. Thermal expansion and transformation behavior of cerium and plutonium alloys: an application of the Aptekar-Ponyatovsky regular solution model

    NASA Astrophysics Data System (ADS)

    Lawson, A. C.; Lashley, J. C.

    2011-09-01

    In this paper we apply the Aptekar-Ponyatovsky (AP) regular solution thermodynamic model to the analysis of experimental data for the coefficient of thermal expansion (CTE) and determine the AP model parameters for unalloyed cerium metal, Ce-Th-La alloys, and Pu-Ga alloys. We find that the high temperature CTE of cerium metal follows the predictions of the AP model based on low temperature, high pressure data. For Ce-Th-La alloys we use the AP parameters to track the suppression of the first-order γ-α cerium transition. We show the AP model accounts for the negative CTE observed for Pu-Ga alloys and is equivalent to an earlier invar model. Finally, we apply the AP parameters obtained for Pu-Ga alloys to rationalize the observed δ-α transformation pressures of these alloys. We show that the anomalous values of the Grüneisen and Grüneisen-Anderson parameters are important features of the thermal properties of plutonium. A strong analogy between the properties of plutonium and cerium is confirmed.

  17. Distributions of 14 elements on 60 selected absorbers from two simulant solutions (acid-dissolved sludge and alkaline supernate) for Hanford HLW Tank 102-SY

    SciTech Connect

    Marsh, S.F.; Svitra, Z.V.; Bowen, S.M.

    1993-10-01

    Sixty commercially available or experimental absorber materials were evaluated for partitioning high-level radioactive waste. These absorbers included cation and anion exchange resins, inorganic exchangers, composite absorbers, and a series of liquid extractants sorbed on porous support-beads. The distributions of 14 elements onto each absorber were measured from simulated solutions that represent acid-dissolved sludge and alkaline supernate solutions from Hanford high-level waste (HLW) Tank 102-SY. The selected elements, which represent fission products (Ce, Cs, Sr, Tc, and Y); actinides (U, Pu, and Am); and matrix elements (Cr, Co, Fe, Mn, Zn, and Zr), were traced by radionuclides and assayed by gamma spectrometry. Distribution coefficients for each of the 1680 element/absorber/solution combinations were measured for dynamic contact periods of 30 min, 2 h, and 6 h to provide sorption kinetics information for the specified elements from these complex media. More than 5000 measured distribution coefficients are tabulated.

  18. Effects of alkoxide addition on the electrochemical deposition and dissolution in triglyme-based solution dissolving magnesium bis(trifluoromethanesulfonyl)amide

    NASA Astrophysics Data System (ADS)

    Kim, In-Tae; Yamabuki, Kazuhiro; Morita, Masayuki; Tsutsumi, Hiromori; Yoshimoto, Nobuko

    2015-03-01

    Electrochemical deposition and dissolution of magnesium (Mg) has been examined in triethylene glycol dimethyl ether (triglyme, G3) dissolving magnesium bis(triflouromethanesulfonyl)amide, Mg(TFSA)2. The voltammetric current responses at platinum (Pt) electrode in the G3-based electrolytes revealed that the Mg deposition/dissolution process depends on the Mg species in the solution phase. The addition of alkoxides, Mg(OCnH2n+1)2, was effective on the reversibility of the process in Mg(TFSA)2/G3. Higher anodic current corresponding to the electrochemical dissolution was observed in the electrolyte solution containing Mg(OC2H5)2 as the additive. The morphology of the Mg deposition at the Pt substrate also depended on the additive Mg-alkoxides. The resulting Mg(TFSA)2/G3 solutions containing Mg-alkoxides were found to be a possible electrolyte system for rechargeable Mg battery operating at ambient temperature.

  19. Polarization-corrosion behavior of commercial gold- and silver-base casting alloys in Fusayama solution.

    PubMed

    Johnson, D L; Rinne, V W; Bleich, L L

    1983-12-01

    Based on polarization measurements, high Au alloys are highly corrosion-resistant and exhibit the lowest corrosion rates; intermediate Au, Ag, and Pd alloys with Cu are passive but exhibit higher corrosion rates. Twenty weight percent (w/o) In-Ag alloys exhibit active corrosion behavior at potentials only 100 mV noble to the corrosion potential.

  20. Impact of air-borne or canopy-derived dissolved organic carbon (DOC) on forest soil solution DOC in Flanders, Belgium

    NASA Astrophysics Data System (ADS)

    Verstraeten, Arne; De Vos, Bruno; Neirynck, Johan; Roskams, Peter; Hens, Maarten

    2014-02-01

    Dissolved organic carbon (DOC) in the soil solution of forests originates from a number of biologically and/or biochemically mediated processes, including litter decomposition and leaching, soil organic matter mineralization, root exudation, mucilage and microbial activity. A variable amount of DOC reaches the forest floor through deposition, but limited information is available about its impact on soil solution DOC. In this study, trends and patterns of soil solution DOC were evaluated in relation to deposition of DOC over an 11-year period (2002-2012) at five ICP Forests intensive monitoring plots in Flanders, northern Belgium. Trend analysis over this period showed an increase of soil solution DOC concentrations for all observed depth intervals. Fluxes of DOC increased in the organic layer, but were nearly stable in the mineral soil. Annual leaching losses of DOC were higher in coniferous (55-61 kg C ha-1) compared to deciduous plots (19-30 kg C ha-1) but embody less than 0.05% of total 1-m soil organic C stocks. Temporal deposition patterns could not explain the increasing trends of soil solution DOC concentrations. Deposition fluxes of DOC were strongly correlated with soil solution fluxes of DOC, but their seasonal peaks were not simultaneous, which confirmed that air-borne or canopy-derived DOC has a limited impact on soil solution DOC.

  1. Effect of volatile elements on porosity formation in solidifying alloys

    NASA Astrophysics Data System (ADS)

    Couturier, G.; Rappaz, M.

    2006-03-01

    Besides dissolved gases such as hydrogen, the partial vapour pressure of volatile solute elements, such as zinc, has been accounted for in equations governing the nucleation and growth of pores in solidifying alloys. In particular, a simple analytical solution giving the porosity fraction as a function of the fraction of solid is proposed. This solution is then used to study the influence of zinc on porosity formation in aluminium- and copper-base alloys. It is shown that the zinc vapour pressure is too low to increase the porosity of aluminium-base alloys, whereas it has a significant effect in brasses. Implementing this contribution into an existing software which calculates the pressure drop in the mushy zone and the segregation of dissolved gases, simulations have been performed in order to assess in more realistic situations the influence of volatile solute elements on porosity.

  2. Fundamental Effects of Aging on Creep Properties of Solution-Treated Low-Carbon N-155 Alloy

    NASA Technical Reports Server (NTRS)

    Frey, D N; Freeman, J W; White, A E

    1950-01-01

    A method is developed whereby the fundamental mechanisms are investigated by which processing, heat treatment, and chemical composition control the properties of alloys at high temperatures. The method used metallographic examination -- both optical and electronic --studies of x-ray diffraction-line widths, intensities, and lattice parameters, and hardness surveys to evaluate fundamental structural conditions. Mechanical properties at high temperatures are then measured and correlated with these measured structural conditions. In accordance with this method, a study was made of the fundamental mechanism by which aging controlled the short-time creep and rupture properties of solution-treated low-carbon n-155 alloy at 1200 degrees F.

  3. Hyaluronic acid stimulates the formation of calcium phosphate on CoCrMo alloy in simulated physiological solution.

    PubMed

    Milošev, Ingrid; Hmeljak, Julija; Cör, Andrej

    2013-03-01

    The behaviour of CoCrMo alloy has been studied in two simulated physiological solutions-NaCl and Hanks' solutions-each containing the sodium salt of hyaluronic acid. Hyaluronic acid is a component of synovial joint fluid, so the behaviour of orthopaedic alloys in its presence needs to be assessed. Electrochemical methods, X-ray photoelectron spectroscopy and scanning electron microscopy have been used to analyse the composition, thickness and morphology of any layers formed on the alloy. The addition of hyaluronic acid shifts the corrosion potential and increases the value of polarization resistance. The presence of hyaluronic acid in simulated Hanks' physiological solution stimulates the formation of a calcium phosphate layer, opening up the possibility for tailoring the surface properties of CoCrMo alloy. The viability of human osteoblast-like was determined using the Alamar(®) Blue Assay, while the osteogenic activity was evaluated by alkaline phosphatase activity. The presence of hyaluronic acid affects the alkaline phosphatase activity.

  4. Hydrogen absorption of titanium and nickel-titanium alloys during long-term immersion in neutral fluoride solution.

    PubMed

    Yokoyama, Ken'ichi; Ogawa, Toshio; Asaoka, Kenzo; Sakai, Jun'ichi

    2006-07-01

    Hydrogen absorption of biomedical titanium and Ni-Ti alloys in a neutral fluoride (2.0% NaF) solution for up to 10,000 h at 37 degrees C has been evaluated by means of hydrogen thermal desorption analysis. For alpha titanium (commercial pure titanium), the amount of absorbed hydrogen was, at most, 10-30 mass ppm, and the corrosion product and hydride formation were revealed on the surface of the specimen by X-ray diffraction analysis. Ni-Ti superelastic alloy absorbed approximately 150 mass ppm of hydrogen, which was probably sufficient to result in the pronounced degradation of the mechanical properties, although corrosion was hardly observed. In contrast, hydrogen absorption of alpha-beta titanium (Ti-6Al-4V) and beta titanium (Ti-11.3Mo-6.6Zr-4.3Sn) alloys was negligible, although general corrosion was observed. The results of the present study indicate that the susceptibility of titanium and Ni-Ti alloys to hydrogen absorption in the neutral fluoride solution is different from that in the acidic fluoride solution reported previously.

  5. Selective separation of copper over solder alloy from waste printed circuit boards leach solution.

    PubMed

    Kavousi, Maryam; Sattari, Anahita; Alamdari, Eskandar Keshavarz; Firozi, Sadegh

    2017-02-01

    The printed circuit boards (PCBs) from electronic waste are important resource, since the PCBs contain precious metals such as gold, copper, tin, silver, platinum and so forth. In addition to the economic point of view, the presence of lead turns this scrap into dangerous to environment. This study was conducted as part of the development of a novel process for selective recovery of copper over tin and lead from printed circuit boards by HBF4 leaching. In previous study, Copper with solder alloy was associated, simultaneously were leached in HBF4 solution using hydrogen peroxide as an oxidant at room temperature. The objective of this study is the separation of copper from tin and lead from Fluoroborate media using CP-150 as an extractant. The influence of organic solvent's concentration, pH, temperature and A/O phase ratio was investigated. The possible extraction mechanism and the composition of the extracted species have been determined. The separation factors for these metals using this agent are reported, while efficient methods for separation of Cu (II) from other metal ions are proposed. The treatment of leach liquor for solvent extraction of copper with CP-150 revealed that 20% CP-150 in kerosene, a 30min period of contact time, and a pH of 3 were sufficient for the extraction of Cu(II) and 99.99% copper was recovered from the leached solution. Copyright © 2016. Published by Elsevier Ltd.

  6. Solid solution strengthening and phase transformation in high-temperature annealed Si80Ge20 alloy

    NASA Astrophysics Data System (ADS)

    Chiang, Tun-Yuan; Wen, Hua-Chiang; Chou, Wu-Ching; Tsai, Chien-Huang

    2014-03-01

    This investigation demonstrates the temperature-dependent mechanical properties of Si80Ge20 alloy films via a nanoindenter in the indentation depth of 100 nm. The roughly equal root mean square roughness (Rrms) values and repeatable load-displacement (P-δ) curves for the samples ensure the mechanical performances mainly contributed from the influences of annealing temperatures. The hardness (H) values of samples increase with the temperatures of an initial annealing in the range from RT to 900 °C, and, conversely, decrease for annealing temperatures over 900 °C. Accordingly, both E/H and hf/hmax values, exhibiting an inverse tendency in the above temperature range, hints that the solid solution strengthening effect and the softening phenomenon occur for the initial-annealing and over-annealing stages, respectively. In addition, grazing incidence X-ray diffraction (GIXRD) analysis demonstrates the lattice expansion and the broadened peak that attribute to the solid solution strengthening of samples and the segregation of Ge, respectively. Through observing the value of the (200) lattice spacing of 5.624 Å for a 900 °C-annealed sample by transmission electron microscopy (TEM) analysis, it is verified that the segregation of Ge is responsible for the decreased hardness for the 1000 °C-annealed sample.

  7. Rapid Assessment of the Influence of Solution pH, Anion Concentration and Temperature on the Dissolution of Alloy 22

    SciTech Connect

    Gray, J J; Hayes, J R; Gdowski, G E; Viani, B E; Orme, C A

    2005-05-19

    We introduce an acid titration technique for the rapid characterization of the influence of solution pH, anion (such as chloride) concentration and temperature on the dissolution of metals. We demonstrate the technique with the characterization of the dissolution of alloy 22 (Ni-22Cr-13Mo-3W-3Fe) exposed to chloride-containing hydrochloric, sulfuric and nitric acid environments as a function of pH (from pH 5 to pH -1) and temperature (25-90 C). A combination of electrochemical techniques (electrochemical impedance spectroscopy and linear polarization resistance) and atomic force microscopy are used to characterize the influence of the various solutions on the dissolution of alloy 22. In solutions containing hydrochloric and sulfuric acids, a critical temperature exists for passive film breakdown on alloy 22 for all environments tested. Below the critical temperature, corrosion rates are less than 1 {micro}m/year. Above the critical temperature, the effect of temperature on dissolution rates is a function of both the pH and chloride content of the solution. In nitric acid containing solutions, the presence of nitrates promotes a stable passive oxide film that inhibits dissolution in all environments tested.

  8. Solid solution decomposition mechanisms in as-cast and microcrystalline Al-Sc alloys: IV. Effect of the decomposition of a solid solution on the mechanical properties of the alloys

    NASA Astrophysics Data System (ADS)

    Chuvil'deev, V. N.; Nokhrin, A. V.; Smirnova, E. S.; Kopylov, V. I.

    2013-09-01

    The effect of the decomposition of the solid solution in Al- X wt % Mg-0.22 wt % Sc-0.15 wt % Zr ( X = 0, 1.5, 4.5 wt %) alloys on their mechanical properties in the as-cast and microcrystalline (MC) states is studied. The contribution of the particles that precipitate during the decomposition to the mechanical properties of the as-cast and MC alloys is determined. For this purpose, the dependences of the volume fraction and the size of the particles precipitating during the decomposition on the annealing time and temperature and the magnesium content in the as-cast and MC alloys are calculated. An additional contribution to the hardening of the MC alloys is shown to be related to the internal stress fields created by the defects that accumulate at the disperse particles distributed in grain boundaries during grain-boundary migration. The calculated macroelasticity limits in the as-cast and MC alloys are compared with the experimental data.

  9. Application of extraction chromatography to the separation of thorium and uranium dissolved in a solution of high salt concentration.

    PubMed

    Fujiwara, Asako; Kameo, Yutaka; Hoshi, Akiko; Haraga, Tomoko; Nakashima, Mikio

    2007-01-26

    Extraction chromatography with commercially available UTEVA resin (for uranium and tetravalent actinide) was applied for the separation of Th and U from control solutions prepared from a multi-element control solution and from sample solutions of solidified simulated waste. Thorium and U in control solutions with 1-5mol/dm(3) HNO(3) were extracted with UTEVA resin and recovered with a solution containing 0.1mol/dm(3) HNO(3) and 0.05mol/dm(3) oxalic acid to be separated from the other metallic elements. Extraction behavior of U in the sample solutions was similar to that in the control solutions, but extraction of Th was dependent on the concentration of HNO(3). Thorium was extracted from 5mol/dm(3) HNO(3) sample solutions but not from 1mol/dm(3) HNO(3) sample solutions. We conjecture that thorium fluoride formation interferes with extraction of Th. Addition of Al(NO(3))(3) and Fe(NO(3))(3), which have higher stability constant with fluoride ion than Th, does improve extractability of Th from 1mol/dm(3) HNO(3) sample solution.

  10. Effect of Phosphate-Buffered Solution Corrosion on the Ratcheting Fatigue Behavior of a Duplex Mg-Li-Al Alloy

    NASA Astrophysics Data System (ADS)

    Yuan, Xin; Yu, Dunji; Gao, Li-Lan; Gao, Hong

    2016-05-01

    This work reports the uniaxial ratcheting and fatigue behavior of a duplex Mg-Li-Al alloy under the influence of phosphate-buffered solution corrosion. Microstructural observations reveal pitting and filament corrosion defects, which impair the load-bearing capacity of the alloy and cause stress concentration, thus leading to an accelerated accumulation of ratcheting strain and shortened fatigue life under the same nominal loading conditions. Comparing Smith model, Smith-Watson-Topper model, and Paul-Sivaprasad-Dhar model, a ratcheting fatigue life prediction model based on the Broberg damage rule and the Paul-Sivaprasad-Dhar model was proposed, and the model yielded a superior prediction for the studied magnesium alloy.

  11. Pressure-induced fcc to hcp phase transition in Ni-based high entropy solid solution alloys

    NASA Astrophysics Data System (ADS)

    Zhang, F. X.; Zhao, Shijun; Jin, Ke; Bei, H.; Popov, D.; Park, Changyong; Neuefeind, J. C.; Weber, W. J.; Zhang, Yanwen

    2017-01-01

    A pressure-induced phase transition from the fcc to a hexagonal close-packed (hcp) structure was found in NiCoCrFe solid solution alloy starting at 13.5 GPa. The phase transition is very sluggish and the transition did not complete at ˜40 GPa. The hcp structure is quenchable to ambient pressure. Only a very small amount (<5%) of hcp phase was found in the isostructural NiCoCr ternary alloy up to the pressure of 45 GPa and no obvious hcp phase was found in NiCoCrFePd system till to 74 GPa. Ab initio Gibbs free energy calculations indicated the energy differences between the fcc and the hcp phases for the three alloys are very small, but they are sensitive to temperature. The critical transition pressure in NiCoCrFe varies from ˜1 GPa at room temperature to ˜6 GPa at 500 K.

  12. In vitro study on the corrosion behavior of three commercial Ag-Pd-Cu-Au alloys in Ringer's and 0.1%Na2S solutions.

    PubMed

    Endo, K; Araki, Y; Kawashima, I; Yamane, Y; Ohno, H; Matsuda, K

    1989-12-01

    The corrosion resistance of three commercial Ag-Pd-Cu-Au alloys was estimated in Ringer's and 0.1% Na2S solutions by electrochemical techniques and surface analyses. In Ringer's solution, the three alloys showed high corrosion resistance and there was no significant difference in the anodic polarization characteristics of the three alloys. In the 0.1% Na2S solution, the Alloy A which had the lowest noble metal content (Au + Pd) exhibited the highest anodic reactivity with the largest amount of corrosion product on the alloy surface. It was determined that the Ag-rich phase of Ag-Pd-Cu-Au alloy was preferentially attacked to form Ag2S corrosion product. The polarization resistance data showed that the corrosion rate for Alloy A in 0.1% Na2S solution was determined to be 500 times higher than that in Ringer's solution. The corrosion rate of the alloy in the freely corroded condition can be estimated quantitatively and precisely by measuring the polarization resistance.

  13. Natural dissolved organic matter mobilizes Cd but does not affect the Cd uptake by the green algae Pseudokirchneriella subcapitata (Korschikov) in resin buffered solutions.

    PubMed

    Verheyen, Liesbeth; Versieren, Liske; Smolders, Erik

    2014-09-01

    Natural dissolved organic matter (DOM) can have contrasting effects on metal bioaccumulation in algae because of complexation reactions that reduce free metal ion concentrations and because of DOM adsorption to algal surfaces which promote metal adsorption. This study was set up to reveal the role of different natural DOM samples on cadmium (Cd) uptake by the green algae Pseudokirchneriella subcapitata (Korschikov). Six different DOM samples were collected from natural freshwater systems and isolated by reverse osmosis. In addition, one (13)C enriched DOM sample was isolated from soil to trace DOM adsorption to algae. Algae were exposed to standardized solutions with or without these DOM samples, each exposed at equal DOM concentrations and at equal non-toxic Cd(2+) activity (∼4 nM) that was buffered with a resin. The DOM increased total dissolved Cd by factors 3-16 due to complexation reactions at equal Cd(2+) activity. In contrast, the Cd uptake was unaffected by DOM or increased maximally 1.6 fold ((13)C enriched DOM). The (13)C analysis revealed that maximally 6% of algal C was derived from DOM and that this can explain the small increase in biomass Cd. It is concluded that free Cd(2+) and not DOM-complexed Cd is the main bioavailable form of Cd when solution Cd(2+) is well buffered. Copyright © 2014 Elsevier B.V. All rights reserved.

  14. Mechanisms of radiation-induced segregation in CrFeCoNi-based single-phase concentrated solid solution alloys

    SciTech Connect

    He, Mo-Rigen; Wang, Shuai; Shi, Shi; Jin, Ke; Bei, Hongbin; Yasuda, Kazuhiro; Matsumura, Syo; Higashida, Kenji; Robertson, Ian M.

    2016-12-31

    Single-phase concentrated solid solution alloys have attracted wide interest due to their superior mechanical properties and enhanced radiation tolerance, which make them promising candidates for the structural applications in next-generation nuclear reactors. However, little has been understood about the intrinsic stability of their as-synthesized, high-entropy configurations against radiation damage. In this paper, we report the element segregation in CrFeCoNi, CrFeCoNiMn, and CrFeCoNiPd equiatomic alloys when subjected to 1250 kV electron irradiations at 400 °C up to a damage level of 1 displacement per atom. Cr/Fe/Mn/Pd can deplete and Co/Ni can accumulate at radiation-induced dislocation loops, while the actively segregating elements are alloy-specific. Moreover, electron-irradiated matrix of CrFeCoNiMn and CrFeCoNiPd shows L10 (NiMn)-type ordering decomposition and <001>-oriented spinodal decomposition between Co/Ni and Pd, respectively. Finally, these findings are rationalized based on the atomic size difference and enthalpy of mixing between the alloying elements, and identify a new important requirement to the design of radiation-tolerant alloys through modification of the composition.

  15. Mechanisms of radiation-induced segregation in CrFeCoNi-based single-phase concentrated solid solution alloys

    DOE PAGES

    He, Mo-Rigen; Wang, Shuai; Shi, Shi; ...

    2016-12-31

    Single-phase concentrated solid solution alloys have attracted wide interest due to their superior mechanical properties and enhanced radiation tolerance, which make them promising candidates for the structural applications in next-generation nuclear reactors. However, little has been understood about the intrinsic stability of their as-synthesized, high-entropy configurations against radiation damage. In this paper, we report the element segregation in CrFeCoNi, CrFeCoNiMn, and CrFeCoNiPd equiatomic alloys when subjected to 1250 kV electron irradiations at 400 °C up to a damage level of 1 displacement per atom. Cr/Fe/Mn/Pd can deplete and Co/Ni can accumulate at radiation-induced dislocation loops, while the actively segregating elementsmore » are alloy-specific. Moreover, electron-irradiated matrix of CrFeCoNiMn and CrFeCoNiPd shows L10 (NiMn)-type ordering decomposition and <001>-oriented spinodal decomposition between Co/Ni and Pd, respectively. Finally, these findings are rationalized based on the atomic size difference and enthalpy of mixing between the alloying elements, and identify a new important requirement to the design of radiation-tolerant alloys through modification of the composition.« less

  16. The Microstructural Evolution of Inconel Alloy 740 During Solution Treatment, Aging, and Exposure at 760 °C

    SciTech Connect

    Cowen, Christopher J.; Danielson, Paul E.; Jablonski, Paul D.

    2010-08-10

    In this study, the microstructural evolution of Inconel alloy 740 during solution treatment and aging was characterized using optical and scanning electron microscopy. During double solution heat treatment, carbon is liberated from the dissolution of MC carbides during the first solution treatment at 1150 °C, and fine MC carbides are precipitated on gamma grain boundaries during the second solution treatment at 1120 °C. Due to the concurrent decrease in carbon solubility and the increase in the contribution of grain boundary diffusion at lower temperatures, the MC carbides on the gamma grain boundaries provide a localized carbon reservoir that aids in M23C6 carbide precipitation on gamma grain boundaries during exposure at 760 °C. The γ' phase, which is the key strengthening phase in alloy 740, is incorporated into the alloy microstructure during aging at 850 °C. Finally, the main source of microstructural instability observed during exposure at 760 °C was the coarsening of the γ' phase.

  17. Reclamation of zinc-contaminated soil using a dissolved organic carbon solution prepared using liquid fertilizer from food-waste composting.

    PubMed

    Chiang, Po-Neng; Tong, Ou-Yang; Chiou, Chyow-San; Lin, Yu-An; Wang, Ming-Kuang; Liu, Cheng-Chung

    2016-01-15

    A liquid fertilizer obtained through food-waste composting can be used for the preparation of a dissolved organic carbon (DOC) solution. In this study, we used the DOC solutions for the remediation of a Zn-contaminated soil (with Zn concentrations up to 992 and 757 mg kg(-1) in topsoil and subsoil, respectively). We then determined the factors that affect Zn removal, such as pH, initial concentration of DOC solution, and washing frequency. Measurements using a Fourier Transform infrared spectrometer (FT-IR) revealed that carboxyl and amide were the major functional groups in the DOC solution obtained from the liquid fertilizer. Two soil washes using 1,500 mg L(-1) DOC solution with a of pH 2.0 at 25°C removed about 43% and 21% of the initial Zn from the topsoil and subsoil, respectively. Following this treatment, the pH of the soil declined from 5.4 to 4.1; organic matter content slightly increased from 6.2 to 6.5%; available ammonium (NH4(+)-N) content increased to 2.4 times the original level; and in the topsoil, the available phosphorus content and the exchangeable potassium content increased by 1.65 and 2.53 times their initial levels, respectively. Copyright © 2015 Elsevier B.V. All rights reserved.

  18. Effect of solution chemistry on the extent of binding of phenanthrene by a soil humic acid: A comparison of dissolved and clay bound humic

    SciTech Connect

    Jones, K.D.; Tiller, C.L.

    1999-02-15

    The effect of pH, ionic strength, and cation in solution on the binding of phenanthrene by a soil humic acid in the aqueous phase was determined using fluorescence quenching. The phenanthrene binding coefficient with the dissolved soil humic, K{sub oc}, decreased with increasing ionic strength and solution cation valence. At low values of ionic strength, K{sub oc} values for this soil humic acid increased with increasing pH. For this humic sample, the experimental results were consistent with a conformational model of the humic substance in aqueous solution where, depending on solution conditions, some parts of the humic structure may be more open to allow increased PAH access to attachment sites. After sorption onto clays, supernatant solutions of the unadsorbed humic fraction yielded lower K{sub oc} values than the original bulk humic acid, suggesting that the humic substance was fractionating during its sorption onto the clays. Additionally, the extent of phenanthrene binding with the adsorbed humic fraction was lower than the results determined for the bulk humic acid prior to adsorption. The conformation of the humic substance when sorbed onto the inorganic surface appears to be affecting the level of phenanthrene binding by the humic acid.

  19. Solute partitioning in TiAl/Ti{sub 3}Al alloys

    SciTech Connect

    Munroe, P.R.; Baker, I.

    1999-11-19

    Over the last few years there have been intense research and development efforts on two-phase alloys based on ({gamma}) TiAl + ({alpha}{sub 2}) Ti{sub 3}Al; the goal being to develop alloys for aerospace and, possibly, automotive applications. Two-phase alloys have been studied which contain numerous elemental additions, the more common ones of which are W, Mo, Nb, Cr, W, V, Si, Mn, Ta, C and B. These have been studied both for their phase stability and to determine their monotonic and cycling loading response both at low and high temperature. Although the mechanical properties and physical behavior of these alloys have been studied in detail, there is surprisingly little published information on the distribution of these alloying additions between the two phases. Here the authors report a short study on two recently developed alloys concerning how some of these elemental additions partition between the two phases.

  20. Tribocorrosion behavior of beta titanium biomedical alloys in phosphate buffer saline solution.

    PubMed

    Pina, V Guiñón; Dalmau, A; Devesa, F; Amigó, V; Muñoz, A Igual

    2015-06-01

    The tribo-electrochemical behavior of different β titanium alloys for biomedical applications sintered by powder metallurgy has been investigated. Different mechanical, electrochemical and optical techniques were used to study the influence of the chemical composition, Sn content, and the electrochemical conditions on the tribocorrosion behavior of those alloys Ti30NbxSn alloys (where "x" is the weight percentage of Sn content, 2% and 4%). Sn content increases the active and passive dissolution rate of the titanium alloys, thus increasing the mechanically activated corrosion under tribocorrosion conditions. It also increases the mechanical wear of the alloy. Prevailing electrochemical conditions between -1 and 2V influences the wear accelerated corrosion by increasing it with the applied potential and slightly increases the mechanical wear of Ti30Nb4Sn. Wear accelerated corrosion can be predicted by existing models as a function of electrochemical and mechanical parameters of the titanium alloys.

  1. Atomic-scale dynamics of edge dislocations in Ni and concentrated solid solution NiFe alloys

    DOE PAGES

    Zhao, Shijun; Osetsky, Yuri N.; Zhang, Yanwen; ...

    2017-01-19

    Single-phase concentrated solid solution alloys (CSAs), including high entropy alloys, exhibit excellent mechanical properties compared to conventional dilute alloys. However, the origin of this observation is not clear yet because the dislocation properties in CSAs are poorly understood. In this work, the mobility of a <110>{111} edge dislocation in pure Ni and equiatomic solid solution Ni0.5Fe0.5 (NiFe) is studied using molecular dynamics simulations with different empirical potentials. The threshold stress to initiate dislocation movement in NiFe is found to be much higher compared to pure Ni. The drag coefficient of the dislocation motion calculated from the linear regime of dislocationmore » velocities versus applied stress suggests that the movement of dislocations in NiFe is strongly damped compared to that in Ni. The present results indicate that the mobility of edge dislocations in fcc CSAs are controlled by the fluctuations in local stacking fault energy caused by the local variation of alloy composition.« less

  2. Elastic stiffness constants of Al-Si and Al-Ge alloys by solid-solutioning under high pressure

    NASA Astrophysics Data System (ADS)

    Soma, Toshinobu; Takashima, Seiji; Kagaya, Hiroko-Matsuo

    1992-02-01

    The elastic stiffness constants of the Al-Si and Al-Ge alloy systems formed by solid solutioning under high pressure are studied using our previous formalism for the static crystal energy term taking account of the lattice dynamical contributions. The obtained results for the temperature-dependence of the elastic constants for pure solvent Al are consistent with the observed data. Then, the atomic fraction-dependence of the elastic constants for these alloy systems is calculated, and a decrease of the elastic stiffness constants C11, C12 and C44 with increasing concentration of Si or Ge is found for both Al-Si and Al-Ge solid solutions. Numerical results of the concentration x-derivative 1/ C ij·d C ij/d x of the elastic constants C ij for the Al 1- xSi x and Al 1- xGe x alloy system are obtained theoretically and found to be nearly constant under pressure and high temperatures. The deviation from the elastic constants of pure Al is larger for the Al-Ge alloy than for the Al-Si system.

  3. Nickel recovery from electronic waste II Electrodeposition of Ni and Ni–Fe alloys from diluted sulfate solutions

    SciTech Connect

    Robotin, B.; Ispas, A.; Coman, V.; Bund, A.; Ilea, P.

    2013-11-15

    Highlights: • Ni can be recovered from EG wastes as pure Ni or as Ni–Fe alloys. • The control of the experimental conditions gives a certain alloy composition. • Unusual deposits morphology shows different nucleation mechanisms for Ni vs Fe. • The nucleation mechanism was progressive for Ni and instantaneous for Fe and Ni–Fe. - Abstract: This study focuses on the electrodeposition of Ni and Ni–Fe alloys from synthetic solutions similar to those obtained by the dissolution of electron gun (an electrical component of cathode ray tubes) waste. The influence of various parameters (pH, electrolyte composition, Ni{sup 2+}/Fe{sup 2+} ratio, current density) on the electrodeposition process was investigated. Scanning electron microscopy (SEM) and X-ray fluorescence analysis (XRFA) were used to provide information about the obtained deposits’ thickness, morphology, and elemental composition. By controlling the experimental parameters, the composition of the Ni–Fe alloys can be tailored towards specific applications. Complementarily, the differences in the nucleation mechanisms for Ni, Fe and Ni–Fe deposition from sulfate solutions have been evaluated and discussed using cyclic voltammetry and potential step chronoamperometry. The obtained results suggest a progressive nucleation mechanism for Ni, while for Fe and Ni–Fe, the obtained data points are best fitted to an instantaneous nucleation model.

  4. Environmentally Assisted Cracking of Alloy 7050-T7451 Exposed to Aqueous Chloride Solutions

    NASA Astrophysics Data System (ADS)

    Braun, Reinhold

    2016-03-01

    The stress corrosion cracking (SCC) behavior of 7050-T7451 plate material was investigated in short-transverse direction performing constant load and constant extension rate tests. Smooth and notched tensile specimens were permanently immersed in substitute ocean water and in an aqueous solution of 0.6 M NaCl + 0.06 M (NH4)2SO4. Alloy 7050-T7451 exhibited high SCC resistance in both synthetic environments. However, conducting cyclic loading tests, environment-induced cracking was observed. Applying a sawtooth waveform, notched tensile specimens were strained under constant load amplitude conditions at constant displacement rates ranging from 2 × 10-6 to 2 × 10-4 mms-1. The stress ratio R = σ min/ σ max was 0.1 with maximum stresses of 300 and 400 MPa. When cyclically loaded in substitute ocean water, notched specimens failed predominantly by transgranular environment-induced cracking. Striations were observed on the cleavage-like facets. The number of cycles-to-failure decreased with decreasing displacement rate. A slope of 0.5 was obtained by fitting the logarithmic plot of number of cycles-to-failure vs nominal loading frequency, indicating a hydrogen embrittlement mechanism controlled by diffusion.

  5. Dispersoid reinforced alloy powder and method of making

    DOEpatents

    Anderson, Iver E.; Terpstra, Robert L.

    2010-04-20

    A method of making dispersion-strengthened alloy particles involves melting an alloy having a corrosion and/or oxidation resistance-imparting alloying element, a dispersoid-forming element, and a matrix metal wherein the dispersoid-forming element exhibits a greater tendency to react with a reactive species acquired from an atomizing gas than does the alloying element. The melted alloy is atomized with the atomizing gas including the reactive species to form atomized particles so that the reactive species is (a) dissolved in solid solution to a depth below the surface of atomized particles and/or (b) reacted with the dispersoid-forming element to form dispersoids in the atomized particles to a depth below the surface of said atomized particles. The atomized alloy particles are solidified as solidified alloy particles or as a solidified deposit of alloy particles. Bodies made from the dispersion strengthened alloy particles, deposit thereof, exhibit enhanced fatigue and creep resistance and reduced wear as well as enhanced corrosion and/or oxidation resistance at high temperatures by virtue of the presence of the corrosion and/or oxidation resistance imparting alloying element in solid solution in the particle alloy matrix.

  6. Dispersoid reinforced alloy powder and method of making

    DOEpatents

    Anderson, Iver E [Ames, IA; Terpstra, Robert L [Ames, IA

    2012-06-12

    A method of making dispersion-strengthened alloy particles involves melting an alloy having a corrosion and/or oxidation resistance-imparting alloying element, a dispersoid-forming element, and a matrix metal wherein the dispersoid-forming element exhibits a greater tendency to react with a reactive species acquired from an atomizing gas than does the alloying element. The melted alloy is atomized with the atomizing gas including the reactive species to form atomized particles so that the reactive species is (a) dissolved in solid solution to a depth below the surface of atomized particles and/or (b) reacted with the dispersoid-forming element to form dispersoids in the atomized particles to a depth below the surface of said atomized particles. The atomized alloy particles are solidified as solidified alloy particles or as a solidified deposit of alloy particles. Bodies made from the dispersion strengthened alloy particles, deposit thereof, exhibit enhanced fatigue and creep resistance and reduced wear as well as enhanced corrosion and/or oxidation resistance at high temperatures by virtue of the presence of the corrosion and/or oxidation resistance imparting alloying element in solid solution in the particle alloy matrix.

  7. Isothermal Decomposition of β-Solid Solution in Titanium Alloy Ti - 10 V - 2Fe - 3Al

    NASA Astrophysics Data System (ADS)

    Illarionov, A. G.; Trubochkin, A. V.; Shalaev, A. M.; Illarionova, S. M.; Popov, A. A.

    2017-03-01

    Regular features of variation of structure, phase composition and hardness characteristics in a β-phase-based titanium alloy Ti - 10 V - 2Fe - 3Al subjected to isothermal treatment in a melt of lead and tin for 5 sec - 32 h at 250 - 800 °C after a hold at 860 °C are considered. The types of the phases precipitated in the process of isothermal decomposition of the high-temperature β-solid solution and the dependences of the lattice constant of the β-phase and of the hardness on the temperature-and-time mode of the treatment are determined. Adiagram of isothermal decomposition of the β-solid solution in alloy Ti - 10 V - 2Fe - 3Al is plotted.

  8. Nickel recovery from electronic waste II electrodeposition of Ni and Ni-Fe alloys from diluted sulfate solutions.

    PubMed

    Robotin, B; Ispas, A; Coman, V; Bund, A; Ilea, P

    2013-11-01

    This study focuses on the electrodeposition of Ni and Ni-Fe alloys from synthetic solutions similar to those obtained by the dissolution of electron gun (an electrical component of cathode ray tubes) waste. The influence of various parameters (pH, electrolyte composition, Ni(2+)/Fe(2+) ratio, current density) on the electrodeposition process was investigated. Scanning electron microscopy (SEM) and X-ray fluorescence analysis (XRFA) were used to provide information about the obtained deposits' thickness, morphology, and elemental composition. By controlling the experimental parameters, the composition of the Ni-Fe alloys can be tailored towards specific applications. Complementarily, the differences in the nucleation mechanisms for Ni, Fe and Ni-Fe deposition from sulfate solutions have been evaluated and discussed using cyclic voltammetry and potential step chronoamperometry. The obtained results suggest a progressive nucleation mechanism for Ni, while for Fe and Ni-Fe, the obtained data points are best fitted to an instantaneous nucleation model.

  9. Fracture of Ni-Ti superelastic alloy under sustained tensile load in physiological saline solution containing hydrogen peroxide.

    PubMed

    Yokoyama, Ken'ichi; Ogawa, Toshio; Fujita, Atsushi; Asaoka, Kenzo; Sakai, Jun'ichi

    2007-09-01

    The fracture of Ni-Ti superelastic alloy has been investigated by a sustained tensile-loading test in physiological saline solution containing hydrogen peroxide (0.15M NaCl + 0.3M H(2)O(2)). The fracture always occurs when the applied stress exceeds the critical stress for martensite transformation. In contrast, under a low applied stress, the fracture does not always occur within 1000 h. The fracture is probably mainly caused by localized corrosion associated with the preferential dissolution of nickel ions. In 0.3M H(2)O(2) solution without NaCl, the fracture does not occur even under a high applied stress. The results of the present study imply that one reason for the fracture of the Ni-Ti superelastic alloy in vivo is localized corrosion due to the synergistic effects of hydrogen peroxide and sodium chloride under applied stress.

  10. Distribution characteristics of dissolved organic carbon in annular wetland soil-water solutions through soil profiles in the Sanjiang Plain, northeast China.

    PubMed

    Xi, Min; Lu, Xian-Guo; Li, Yue; Kong, Fan-Long

    2007-01-01

    Overwhelming evidence reveals that concentrations of dissolved organic carbon (DOC) have increased in streams which brings negative environmental impacts. DOC in stream flow is mainly originated from soil-water solutions of watershed. Wetlands prove to be the most sensitive areas as an important DOC reserve between terrestrial and fluvial biogeosystems. This reported study was focused on the distribution characteristics and the controlling factors of DOC in soil-water solutions of annular wetland, i.e., a dishing wetland and a forest wetland together, in the Sanjiang Plain, Northeast China. The results indicate that DOC concentrations in soil-water solutions decreased and then increased with increasing soil depth in the annular wetland. In the upper soil layers of 0-10 cm and 10-20 cm, DOC concentrations in soil-water solutions linearly increased from edge to center of the annular wetland (R2 = 0.3122 and R2 = 0.443). The distribution variations were intimately linked to DOC production and utilization and DOC transport processes in annular wetland soil-water solutions. The concentrations of total organic carbon (TOC), total carbon (TC) and Fe(II), DOC mobility and continuous vertical and lateral flow affected the distribution variations of DOC in soil-water solutions. The correlation coefficients between DOC concentrations and TOC, TC and Fe(II) were 0.974, 0.813 and 0.753 respectively. These distribution characteristics suggested a systematic response of the distribution variations of DOC in annular wetland soil-water solutions to the geometry of closed depressions on a scale of small catchments. However, the DOC in soil pore water of the annular wetland may be the potential source of DOC to stream flow on watershed scale. These observations also implied the fragmentation of wetland landscape could bring the spatial-temporal variations of DOC distribution and exports, which would bring negative environmental impacts in watersheds of the Sanjiang Plain.

  11. Effect of Organic Acid Additions on the General and Localized Corrosion Susceptibility of Alloy 22 in Chloride Solutions

    SciTech Connect

    Carranza, R M; Giordano, C M; Rodr?guez, M A; Ilevbare, G O; Rebak, R B

    2007-08-28

    Electrochemical studies such as cyclic potentiodynamic polarization (CPP) and electrochemical impedance spectroscopy (EIS) were performed to determine the corrosion behavior of Alloy 22 (N06022) in 1M NaCl solutions at various pH values from acidic to neutral at 90 C. All the tested material was wrought Mill Annealed (MA). Tests were also performed in NaCl solutions containing weak organic acids such as oxalic, acetic, citric and picric. Results show that the corrosion rate of Alloy 22 was significantly higher in solutions containing oxalic acid than in solutions of pure NaCl at the same pH. Citric and picric acids showed a slightly higher corrosion rate, and acetic acid maintained the corrosion rate of pure chloride solutions at the same pH. Organic acids revealed to be weak inhibitors for crevice corrosion. Higher concentration ratios, compared to nitrate ions, were needed to completely inhibit crevice corrosion in chloride solutions. Results are discussed considering acid dissociation constants, buffer capacity and complex formation constants of the different weak acids.

  12. Reclamation of copper-contaminated soil using EDTA or citric acid coupled with dissolved organic matter solution extracted from distillery sludge.

    PubMed

    Liu, Cheng-Chung; Lin, Ying-Chen

    2013-07-01

    Soil washing using a strong chelating agent is a common practice for restoring contaminated soils, but significant soil fertility degradation and high operation costs are the major disadvantages. Washing soil with a dissolved organic matter (DOM) solution has been identified as a method that can moderate the loss of nutrients in the soil and enhance metal removal. The DOM solutions were extracted from waste sludge obtained from a local whisky distillery. Single chelating washing and chelate-DOM washing were carried out using ethylenediaminetetraacetic acid (EDTA), citric acid, and DOM solutions to remediate highly Cu-contaminated soil. Two-phase washing using 0.34 M citric acid and then 1500 mg L(-1) DOM solution (pH 8.5) was found to be most favorable for the soil. With this treatment, 91% Cu was removed from the topsoil; the organic matter, cation exchange capacity, plant-available nitrogen, and available phosphate content increased by 28.1%, 103%, 17.7%, and 422%, respectively. Copyright © 2013 Elsevier Ltd. All rights reserved.

  13. Acid neutralizing processes in an alpine watershed front range, Colorado, U.S.A.-1: Buffering capacity of dissolved organic carbon in soil solutions

    USGS Publications Warehouse

    Iggy, Litaor M.; Thurman, E.M.

    1988-01-01

    Soil interstitial waters in the Green Lakes Valley, Front Range, Colorado were studied to evaluate the capacity of the soil system to buffer acid deposition. In order to determine the contribution of humic substances to the buffering capacity of a given soil, dissolved organic carbon (DOC) and pH of the soil solutions were measured. The concentration of the organic anion, Ai-, derived from DOC at sample pH and the concentration of organic anion, Ax- at the equivalence point were calculated using carboxyl contents from isolated and purified humic material from soil solutions. Subtracting Ax- from Ai- yields the contribution of humic substances to the buffering capacity (Aequiv.-). Using this method, one can evaluate the relative contribution of inorganic and organic constituents to the acid neutralizing capacity (ANC) of the soil solutions. The relative contribution of organic acids to the overall ANC was found to be extremely important in the alpine wetland (52%) and the forest-tundra ecotone (40%), and somewhat less important in the alpine tundra sites (20%). A failure to recognize the importance of organic acids in soil solutions to the ANC will result in erroneous estimates of the buffering capacity in the alpine environment of the Front Range, Colorado. ?? 1988.

  14. Influence of potential on the electrochemical behaviour of beta titanium alloys in Hank's solution.

    PubMed

    Karthega, M; Raman, V; Rajendran, N

    2007-11-01

    The electrochemical behaviour of beta titanium alloys, namely Ti-15Mo (TiMo) and Ti-29Nb-13Ta-4.6Zr (TNTZ), were studied under physiological conditions using open circuit potential (OCP), potentiodynamic polarization and electrochemical impedance spectroscopic (EIS) measurements. The OCP data for TNTZ alloy indicated a noble behaviour compared to TiMo alloy. The current density value for TNTZ alloy calculated from polarization measurement was found to be comparable to that of TiMo. The EIS technique was applied to study the nature of the passive film formed on binary TiMo alloy at various impressed potentials and the results were compared with that of the quaternary TNTZ alloy. The EIS spectra obtained for TiMo alloy exhibited a single time constant for all potentials, indicating a highly compact passive layer over the surface. The TNTZ alloy, however, exhibited a single time constant at lower potentials and two time constants at higher potentials, indicating a bilayer structure at higher potentials.

  15. Corrosion behaviour of polished and sandblasted titanium alloys in PBS solution.

    PubMed

    Burnat, Barbara; Walkowiak-Przybyło, Magdalena; Błaszczyk, Tadeusz; Klimek, Leszek

    2013-01-01

    In this work, we performed comparative studies of the effect of surface preparation of Ti6Al4V and Ti6Al7Nb biomedical alloys and the influence of endothelial cells on their corrosion behaviour in PBS (Phosphate Buffered Saline). Two different methods of surface modification were applied - polishing and sandblasting. The polished Ti6Al7Nb alloy was found to have the best resistance against general corrosion in PBS. It was characterized by the lowest corrosion rate, the widest passive range and the lowest reactivity. Both alloys prepared by sandblasting exhibited worse corrosion properties in comparison to the polished ones. This can be associated with a greater development of their surface and the presence of Al2O3 grains which caused an increase of corrosion potential but might also influence the weakening of the passive layer. Results of potentiodynamic anodic polarization indicated that more resistant to pitting corrosion was Ti6Al7Nb alloy regardless of the method of surface preparation. In those cases, anodic polarization caused only an increase of passive layer, while in the case of sandblasted Ti6Al4V alloy it caused a pitting corrosion. The results obtained allowed us to conclude that the niobium-titanium alloys had higher corrosion resistance than titanium alloys with vanadium. Moreover, it was stated that endothelial cells improved the corrosion resistance of all the titanium alloys examined.

  16. Localized Recrystallization in Cast Al-Si-Mg Alloy during Solution Heat Treatment: Dilatometric and Calorimetric Studies

    NASA Astrophysics Data System (ADS)

    Chaudhury, S. K.; Warke, V.; Shankar, S.; Apelian, D.

    2011-10-01

    During heat treatment, the work piece experiences a range of heating rates depending upon the sizes and types of furnace. When the Al-Si-Mg cast alloy is heated to the solutionizing temperature, recrystallization takes place during the ramp-up stage. The effect of heating rate on recrystallization in the A356 (Al-Si-Mg) alloy was studied using dilatometric and calorimetric methods. Recrystallization in as-cast Al-Si alloys is a localized event and is confined to the elasto-plastic zone surrounding the eutectic Si phase; there is no evidence of recrystallization in the center of the primary Al dendritic region. The size of the elasto-plastic zone is of the same order of magnitude as the Si particles, and recrystallized grains are observed in the elasto-plastic region near the Si particles. The coefficient of thermal expansion of Al is an order of magnitude greater than Si, and thermal stresses are generated due to the thermal mismatch between the Al phase and Si particles providing the driving force for recrystallization. In contrast, recrystallization in Al wrought alloy (7075) occurs uniformly throughout the matrix, stored energy due to cold work being the driving force for recrystallization in wrought alloys. The activation energy for recrystallization in as-cast A356 alloy is 127 KJ/mole. At a slow heating rate of 4.3 K/min, creep occurs during the heating stage of solution heat treatment. However, creep does not occur in samples heated at higher heating rates, namely, 520, 130, and 17.3 K/min.

  17. Environmentally assisted cracking of two-phase Fe-Mn-Al alloys in NaCl solution

    NASA Astrophysics Data System (ADS)

    Shih, S.-T.; Tsu, I.-F.; Perng, T.-P.

    1993-02-01

    Three two-phase Fe-Mn-Al alloys with nominal compositions, Fe-24Mn-9Al, Fe-27Mn-9Al-3Cr,. and Fe-27Mn-9Al-6Cr, were prepared in the solution-treated and cold-rolled conditions. The fractions of ferrite in the solution-treated condition were controlled at 46 to 60 pct, mainly by adjusting the carbon content and the relative amounts of Mn and Al. The ferrite fractions were reduced to 30 to 37 pct after 75 pct deformation by cold-rolling. Specimens were tensile tested at open circuit in aerated 3.5 pct NaCl solution at slow strain rates ranging from 4 × 10-7 to 4 × 10-5 s-1 at room temperature. All of the alloys were quite susceptible to environmentally assisted cracking (EAC). The deformed specimens showed less susceptibility, presumably because the plasticity was already too limited. The EAC appeared to occur at or after the onset of plastic deformation. In this alloy system, the ferritic phase was less resistant to EAC than the austenitic phase, in contrast to the Fe-Cr-Ni stainless steels. The crack propagated preferentially through the ferrite grains or along the ferrite/austenite grain boundaries. The addition of up to 6 pct Cr did not improve the EAC resistance.

  18. Inhibition of hydrogen embrittlement of Ni-Ti superelastic alloy in acid fluoride solution by hydrogen peroxide addition.

    PubMed

    Yokoyama, Ken'ichi; Yazaki, Yushin; Sakai, Jun'ichi

    2011-09-01

    Inhibition of the hydrogen embrittlement of Ni-Ti superelastic alloy in an acidulated phosphate fluoride (APF) solution has been attempted by adding various amounts of H(2)O(2). In a 0.2% APF solution, hydrogen absorption is markedly inhibited by adding H(2)O(2), although corrosion is slightly enhanced by increasing the amount of added H(2)O(2). By adding a small amount of H(2)O(2) (0.001 M), in the early stage of immersion, hydrogen embrittlement is inhibited and corrosion is only slightly enhanced. Upon adding H(2)O(2), it appears that the dominant cathodic reactions change from hydrogen evolution to H(2)O(2) reduction reactions, or the surface conditions of the alloy are changed by H(2)O(2) with a high oxidation capability, thereby inhibiting hydrogen absorption. The present study clearly indicates that infinitesimal addition of H(2)O(2) into acid fluoride solutions is effective for the inhibition of the hydrogen embrittlement of the alloy.

  19. Corrosion and corrosion inhibition of Al and some alloys in sulphate solutions containing halide ions investigated by an impedance technique

    NASA Astrophysics Data System (ADS)

    Rehim, Sayed S. Abdel; Hassan, Hamdi H.; Amin, Mohammed A.

    2002-02-01

    This paper reports the results of impedance measurements on the corrosion behaviour of pure Al, (Al+6%Cu) and (Al+6%Si) alloys in Na 2SO 4 solutions in the absence and presence of NaCl, NaBr and NaI under the influence of various experimental variables at the open circuit potential (OCP). We find that in the absence of halide ions the rates of corrosion of the three Al samples are enhanced with increasing concentration, acidity, and alkalinity of the Na 2SO 4 solution and in the presence of halide ions. The corrosion resistance increases in the order Al<(Al+6%Cu)<(Al+6%Si). The aggressiveness of the halide ions towards the corrosion of Al and its two alloys increases in the order: I -
    alloys in (0.5 M Na 2SO 4+0.2 M NaCl) solution (except NO 3-) are to inhibit the corrosion of the three samples to an extent depending on the nature of the inhibitor.

  20. Surface micro-dissolve method of imparting self-cleaning property to cotton fabrics in NaOH/urea aqueous solution

    NASA Astrophysics Data System (ADS)

    Fan, Tao; Hu, Ruimin; Zhao, Zhenyun; Liu, Yiping; Lu, Ming

    2017-04-01

    A simple and economical micro-dissolved process of embedding titanium dioxide (TiO2) nanoparticles into surface zone of cotton fabrics was developed. TiO2 was coated on cotton fabrics in 7% wt NaOH/12% wt urea aqueous solution at low temperature. Photocatalytic efficiency of cotton fabrics treated with TiO2 nanoparticles was studied upon measuring the photocatalytic decoloration of Rhodamine B (RhB) under ultraviolet irradiation. Self-cleaning property of cotton fabric coated with TiO2 was evaluated with color depth of samples (K/S value). The treated fabrics were characterized using scanning electron microscopy (SEM), energy dispersive spectrometer (EDS), Fourier transform infrared spectroscopy (FITR), tensile strength, stiffness and whiteness. The results indicated, TiO2 nanoparticles could be embedded on the surface layer of cotton fabrics throuth surface micro-dissolve method. Treated cotton fabrics possessed distinct photocatalytic efficiency and self-cleaning properties. Tensile strength and whiteness of modified cotton fabrics appeared moderately increasement.

  1. Quantification of the dissolved inorganic carbon species and of the pH of alkaline solutions exposed to CO2 under pressure: a novel approach by Raman scattering.

    PubMed

    Beuvier, Thomas; Calvignac, Brice; Bardeau, Jean-François; Bulou, Alain; Boury, Frank; Gibaud, Alain

    2014-10-07

    Dissolved inorganic carbon (DIC) content of aqueous systems is a key function of the pH, of the total alkanility (TA), and of the partial pressure of CO2. However, common analytical techniques used to determine the DIC content in water are unable to operate under high CO2 pressure. Here, we propose to use Raman spectroscopy as a novel alternative to discriminate and quantitatively monitor the three dissolved inorganic carbon species CO2(aq), HCO3(-), and CO3(2-) of alkaline solutions under high CO2 pressure (from P = 0 to 250 bar at T = 40 °C). In addition, we demonstrate that the pH values can be extracted from the molalities of CO2(aq) and HCO3(-). The results are in very good agreement with those obtained from direct spectrophotometric measurements using colored indicators. This novel method presents the great advantage over high pressure conventional techniques of not using breakable electrodes or reference additives and appears of great interest especially in marine biogeochemistry, in carbon capture and storage and in material engineering under high CO2 pressure.

  2. Attractive forces between hydrophobic solid surfaces measured by AFM on the first approach in salt solutions and in the presence of dissolved gases.

    PubMed

    Azadi, Mehdi; Nguyen, Anh V; Yakubov, Gleb E

    2015-02-17

    Interfacial gas enrichment of dissolved gases (IGE) has been shown to cover hydrophobic solid surfaces in water. The atomic force microscopy (AFM) data has recently been supported by molecular dynamics simulation. It was demonstrated that IGE is responsible for the unexpected stability and large contact angle of gaseous nanobubbles at the hydrophobic solid-water interface. Here we provide further evidence of the significant effect of IGE on an attractive force between hydrophobic solid surfaces in water. The force in the presence of dissolved gas, i.e., in aerated and nonaerated NaCl solutions (up to 4 M), was measured by the AFM colloidal probe technique. The effect of nanobubble bridging on the attractive force was minimized or eliminated by measuring forces on the first approach of the AFM probe toward the flat hydrophobic surface and by using high salt concentrations to reduce gas solubility. Our results confirm the presence of three types of forces, two of which are long-range attractive forces of capillary bridging origin as caused by either surface nanobubbles or gap-induced cavitation. The third type is a short-range attractive force observed in the absence of interfacial nanobubbles that is attributed to the IGE in the form of a dense gas layer (DGL) at hydrophobic surfaces. Such a force was found to increase with increasing gas saturation and to decrease with decreasing gas solubility.

  3. Microstructure and corrosion behavior of die-cast AM60B magnesium alloys in a complex salt solution. A slow positron beam study

    SciTech Connect

    Liu, Y. F.; Yang, W.; Qin, Q. L.; Wen, W.; Zhai, T.; Yu, B.; Liu, D. Y.; Luo, A.; Song, GuangLing

    2013-12-15

    The microstructure and corrosion behavior of high pressure die-cast (HPDC) and super vacuum die-cast (SVDC) AM60B magnesium alloys were investigated in a complex salt solution using slow positron beam technique and potentiodynamic polarization tests. The experiments revealed that a CaCO3 film was formed on the surface of the alloys and that the rate of CaCO3 formation for the SVDC alloy with immersion time was slower than that of the HPDC alloy. The larger volume fraction of b-phase in the skin layer of the SVDC alloy than that of the HPDC alloy was responsible for the better corrosion resistance.

  4. Electrophoretic painting on AZ31 Mg alloy pretreated in cerium conversion coating solutions prepared in ethanol-water mixtures

    NASA Astrophysics Data System (ADS)

    Van Phuong, Nguyen; Fazal, Basit Raza; Moon, Sungmo

    2017-01-01

    Electrophoretic painting (E-paint) was prepared on AZ31 Mg alloy samples pretreated in cerium conversion coating (CeCC) solutions with various ratios of ethanol and water mixture and its characteristics, adhesion and corrosion resistance were investigated. It was found that CeCC formed on AZ31 Mg alloy in a CeCC solution without ethanol was partly cracked structure and mainly consisted of Mg(OH)2/MgO, which exhibited weak adhesion with E-painting layer after water immersion test, and low corrosion resistance, as indicated by rapid formation of blisters and paint delamination during salt spray test. The addition of ethanol promoted the growth of a fine nano-crystalline CeO2 layer over the entire substrate surface. The E-paint on AZ31 pretreated in the CeCC solutions with addition of ethanol showed also improved corrosion resistance, as represented by the delayed time for paint delamination and blister formation. The E-paint layers on the CeCC layers formed in solutions containing 50-80 vol% ethanol showed stronger adhesion and better corrosion resistance than those formed on the samples treated in a non-ethanol containing CeCC solution.

  5. Nanosize-induced drastic drop in equilibrium hydrogen pressure for hydride formation and structural stabilization in Pd-Rh solid-solution alloys.

    PubMed

    Kobayashi, Hirokazu; Morita, Hitoshi; Yamauchi, Miho; Ikeda, Ryuichi; Kitagawa, Hiroshi; Kubota, Yoshiki; Kato, Kenichi; Takata, Masaki; Toh, Shoichi; Matsumura, Syo

    2012-08-01

    We have synthesized and characterized homogeneous solid-solution alloy nanoparticles of Pd and Rh, which are immiscible with each other in the equilibrium bulk state at around room temperature. The Pd-Rh alloy nanoparticles can absorb hydrogen at ambient pressure and the hydrogen pressure of Pd-Rh alloys for hydrogen storage is dramatically decreased by more than 4 orders of magnitude from the corresponding pressure in the metastable bulk state. The solid-solution state is still maintained in the nanoparticles even after hydrogen absorption/desorption, in contrast to the metastable bulks which are separated into Pd and Rh during the process.

  6. Adsorbed poly(aspartate) coating limits the adverse effects of dissolved groundwater solutes on Fe(0) nanoparticle reactivity with trichloroethylene.

    PubMed

    Phenrat, Tanapon; Schoenfelder, Daniel; Kirschling, Teresa L; Tilton, Robert D; Lowry, Gregory V

    2015-08-02

    For in situ groundwater remediation, polyelectrolyte-modified nanoscale zerovalent iron particles (NZVIs) have to be delivered into the subsurface, where they degrade pollutants such as trichloroethylene (TCE). The effect of groundwater organic and ionic solutes on TCE dechlorination using polyelectrolyte-modified NZVIs is unexplored, but is required for an effective remediation design. This study evaluates the TCE dechlorination rate and reaction by-products using poly(aspartate) (PAP)-modified and bare NZVIs in groundwater samples from actual TCE-contaminated sites in Florida, South Carolina, and Michigan. The effects of groundwater solutes on short- and intermediate-term dechlorination rates were evaluated. An adsorbed PAP layer on the NZVIs appeared to limit the adverse effect of groundwater solutes on the TCE dechlorination rate in the first TCE dechlorination cycle (short-term effect). Presumably, the pre-adsorption of PAP "trains" and the Donnan potential in the adsorbed PAP layer prevented groundwater solutes from further blocking NZVI reactive sites, which appeared to substantially decrease the TCE dechlorination rate of bare NZVIs. In the second and third TCE dechlorination cycles (intermediate-term effect), TCE dechlorination rates using PAP-modified NZVIs increased substantially (~100 and 200%, respectively, from the rate of the first spike). The desorption of PAP from the surface of NZVIs over time due to salt-induced desorption is hypothesized to restore NZVI reactivity with TCE. This study suggests that NZVI surface modification with small, charged macromolecules, such as PAP, helps to restore NZVI reactivity due to gradual PAP desorption in groundwater.

  7. Persistence of two neonicotinoid insecticides in wastewater, and in aqueous solutions of surfactants and dissolved organic matter.

    PubMed

    Peña, A; Rodríguez-Liébana, J A; Mingorance, M D

    2011-07-01

    Wastewater treatment plants receive organic contaminants, such as pesticides, which reach the sewage system from domestic, industrial or agricultural activities. In wastewater, which is a complex mixture of organic and inorganic compounds, biotic or abiotic degradation of contaminants can be affected by the presence of co-solutes. The photodecomposition in natural sunlight of two neonicotinoid insecticides, thiamethoxam and thiacloprid, was investigated in wastewater, aqueous extracts of sewage sludge and in aqueous surfactant solutions, which are abundant in wastewater. Dissipation in the dark was also studied in wastewater, due to reduction of transmitted sunlight in wastewater ponds. With regard to photolysis, thiamethoxam degraded rapidly in all the aqueous solutions. Among them sewage sludge extracts slightly modified (average half-life 17.6h), wastewater increased (13.7h) and non-ionic surfactants led, as a family, to the highest dissipation rates (average 6.2h), with respect to control water (18.7h). Additionally this pesticide also underwent a slower biodegradation process in wastewater in the dark under anaerobic conditions (around 25d). A metabolite of thiamethoxam from the biological decomposition in wastewater was identified by HPLC/MS. On the other hand thiacloprid was found to be resistant to photo- and biodecomposition and remained almost unchanged during the experimental periods in all the tested media.

  8. Probing liquation cracking and solidification through modeling of momentum, heat, and solute transport during welding of aluminum alloys

    NASA Astrophysics Data System (ADS)

    Mishra, S.; Chakraborty, S.; DebRoy, T.

    2005-05-01

    A transport phenomena-based mathematical model is developed to understand liquation cracking in weldments during fusion welding. Equations of conservation of mass, momentum, heat, and solute transport are numerically solved considering nonequilibrium solidification and filler metal addition to determine the solid and liquid phase fractions in the solidifying region and the solute distribution in the weld pool. An effective partition coefficient that considers the local interface velocity and the undercooling is used to simulate solidification during welding. The calculations show that convection plays a dominant role in the solute transport inside the weld pool. The predicted weld-metal solute content agreed well with the independent experimental observations. The liquation cracking susceptibility in Al-Cu alloy weldments could be reliably predicted by the model based on the computed solidifying weld-metal composition and solid fraction considering nonequilibrium solidification.

  9. Evaluation of Solid-Solution Hardening in Several Binary Alloy Systems Using Diffusion Couples Combined with Nanoindentation

    NASA Astrophysics Data System (ADS)

    Kadambi, Sourabh B.; Divya, V. D.; Ramamurty, U.

    2017-10-01

    Analysis of solid-solution hardening (SSH) in alloys requires the synthesis of large composition libraries and the measurement of strength or hardness from these compositions. Conventional methods of synthesis and testing, however, are not efficient and high-throughput approaches have been developed in the past. In the present study, we use a high-throughput combinatorial approach to examine SSH at large concentrations in binary alloys of Fe-Ni, Fe-Co, Pt-Ni, Pt-Co, Ni-Co, Ni-Mo, and Co-Mo. The diffusion couple (DC) method is used to generate concentration ( c) gradients and the nanoindentation (NI) technique to measure the hardness ( H) along these gradients. The obtained H -c profiles are analyzed within the framework of the Labusch model of SSH, and the c^{2/3} dependence of H predicted by the model is found to be generally applicable. The SSH behavior obtained using the combinatorial method is found to be largely consistent with that observed in the literature using conventional and DC-NI methods. This study evaluates SSH in Fe-, Ni-, Co-, and Pt-based binary alloys and confirms the applicability of the DC-NI approach for rapidly screening various solute elements for their SSH ability.

  10. Metal release and speciation of released chromium from a biomedical CoCrMo alloy into simulated physiologically relevant solutions.

    PubMed

    Hedberg, Yolanda; Odnevall Wallinder, Inger

    2014-05-01

    The objective of this study was to investigate the extent of released Co, Cr(III), Cr(VI), and Mo from a biomedical high-carbon CoCrMo alloy exposed in phosphate-buffered saline (PBS), without and with the addition of 10 µM H2 O2 (PBS + H2 O2 ), and 10 g L(-1) bovine serum albumin (PBS + BSA) for time periods up to 28 days. Comparative studies were made on AISI 316L for the longest time period. No Cr(VI) release was observed for any of the alloys in either PBS or PBS + H2 O2 at open-circuit potential (no applied potential). However, at applied potentials (0.7 V vs. Ag/AgCl), Cr was primarily released as Cr(VI). Co was preferentially released from the CoCrMo alloy at no applied potential. As a consequence, Cr was enriched in the utmost surface oxide reducing the extent of metal release over time. This passivation effect was accelerated in PBS + H2 O2 . As previously reported for 316L, BSA may also enhance metal release from CoCrMo. However, this was not possible to verify due to the precipitation of metal-protein complexes with reduced metal concentrations in solution as a consequence. This was particularly important for Co-BSA complexes after sufficient time and resulted in an underestimation of metals in solution. Copyright © 2013 Wiley Periodicals, Inc.

  11. Effects of Solute Redistribution on the Structure and Properties of Cast Alloys

    DTIC Science & Technology

    1976-08-01

    energy on microstructure (if any) is being measured. The metallographic investigation of samples after creep testing is underway. The first work on...sections of this report deal with the analysis method of the continuous casting simulaton. The remaining alloy work deals with titanium and NITINOL . The...titanium work will evaluate the tendency of these alloys to exhibit macrosegregation as a result of the bulk movement of enriched liquid. The NITINOL

  12. Whole body postmortem angiography with a high viscosity contrast agent solution using poly ethylene glycol as contrast agent dissolver.

    PubMed

    Jackowski, Christian; Persson, Anders; Thali, Michael J

    2008-03-01

    Postmortem minimal invasive angiography has already been implemented to support virtual autopsy examinations. An experimental approach in a porcine model to overcome an initially described artificial tissue edema artifact by using a poly ethylene glycol (PEG) containing contrast agent solution showed promising results. The present publication describes the first application of PEG in a whole corpse angiographic CT examination. A minimal invasive postmortem CT angiography was performed in a human corpse utilizing the high viscosity contrast agent solution containing 65% of PEG. Injection was carried out via the femoral artery into the aortic root in simulated cardiac output conditions. Subsequent CT scanning delivered the 3D volume data of the whole corpse. Visualization of the human arterial anatomy was excellent and the contrast agent distribution was generally limited to the arterial system as intended. As exceptions an enhancement of the brain, the left ventricular myocardium and the renal cortex became obvious. This most likely represented the stage of centralization of the blood circulation at the time of death with dilatation of the precapillary arterioles within these tissues. Especially for the brain this resulted in a distinctively improved visualization of the intracerebral structures by CT. However, the general tissue edema artifact of postmortem minimal invasive angiography examinations could be distinctively reduced.

  13. A relationship to estimate the excess entropy of mixing: Application in silicate solid solutions and binary alloys

    PubMed Central

    Benisek, Artur; Dachs, Edgar

    2012-01-01

    The paper presents new calorimetric data on the excess heat capacity and vibrational entropy of mixing of Pt–Rh and Ag–Pd alloys. The results of the latter alloy are compared to those obtained by calculations using the density functional theory. The extent of the excess vibrational entropy of mixing of these binaries and of some already investigated binary mixtures is related to the differences of the end-member volumes and the end-member bulk moduli. These quantities are used to roughly represent the changes of the bond length and stiffness in the substituted and substituent polyhedra due to compositional changes, which are assumed to be the important factors for the non-ideal vibrational behaviour in solid solutions. PMID:23471516

  14. Effects of cupric ions on the corrosion behavior of aluminum alloy 5A02 in ethylene glycol-water solution

    NASA Astrophysics Data System (ADS)

    Gao, Shu-lun; Yu, Mei; Liu, Jian-hua; Xue, Bing; Li, Song-mei

    2017-04-01

    The effects of cupric ions on the corrosion behavior of aluminum alloy 5A02 in ethylene glycol-water solutions were studied by potentiodynamic polarization, electrochemical noise (EN), and complementary techniques including scanning electron microscopy (SEM), atomic force microscopy (AFM), and X-ray photoelectron spectroscopy (XPS). A positive corrosion potential and increased corrosion current were observed due to the deposition of copper. The results demonstrate that the main corrosion type was pitting and the increasing cupric ion concentration augmented the pitting density. The pits became larger and deeper as a result of the embedment of copper into the surface of the alloy. Cupric ions were preferentially deposited at the defects around the secondary phase, leading to the formation of Al-Cu microgalvanic couples, which increased the corrosion rate. The corrosion rate gradually reached a stable value as the concentration of cupric ions was increased beyond 10 mmol/L.

  15. Corrosion Inhibition Performance of Triazole Derivatives on Copper-Nickel Alloy in 3.5 wt.% NaCl Solution

    NASA Astrophysics Data System (ADS)

    Jiang, B.; Jiang, S. L.; Liu, X.; Ma, A. L.; Zheng, Y. G.

    2015-12-01

    This study investigates the performance of three triazole derivatives with different molecular structures as corrosion inhibitors for the copper-nickel alloy CuNi 90/10 in 3.5 wt.% NaCl solution. Inhibition behavior was systematically determined through electrochemical measurements, scanning electron microscopy, energy-dispersive spectroscopy, and Fourier transform infrared spectroscopy. In addition, adsorption behavior and the inhibition mechanism were investigated via quantum chemical calculation and molecular dynamic simulation. Experimental results indicate that the three inhibitors with triazole rings and heteroatoms exhibited excellent corrosion inhibition capabilities on the copper-nickel alloy surface through physisorption and chemisorption. In particular, 3-amino-5-mercapto-1,2,4-triazole showed the best inhibition capability according to the concentration ranges considered in the experiments. The results of quantum chemical calculation agreed with the experimental findings.

  16. A relationship to estimate the excess entropy of mixing: Application in silicate solid solutions and binary alloys.

    PubMed

    Benisek, Artur; Dachs, Edgar

    2012-06-25

    The paper presents new calorimetric data on the excess heat capacity and vibrational entropy of mixing of Pt-Rh and Ag-Pd alloys. The results of the latter alloy are compared to those obtained by calculations using the density functional theory. The extent of the excess vibrational entropy of mixing of these binaries and of some already investigated binary mixtures is related to the differences of the end-member volumes and the end-member bulk moduli. These quantities are used to roughly represent the changes of the bond length and stiffness in the substituted and substituent polyhedra due to compositional changes, which are assumed to be the important factors for the non-ideal vibrational behaviour in solid solutions.

  17. Development and Characterization of Improved NiTiPd High-Temperature Shape-Memory Alloys by Solid-Solution Strengthening and Thermomechanical Processing

    NASA Technical Reports Server (NTRS)

    Bigelow, Glen; Noebe, Ronald; Padula, Santo, II; Garg, Anita; Olson, David

    2006-01-01

    The need for compact, solid-state actuation systems for use in the aerospace, automotive, and other transportation industries is currently motivating research in high-temperature shape-memory alloys (HTSMA) with transformation temperatures greater than 100 C. One of the basic high-temperature alloys investigated to fill this need is Ni(19.5)Ti(50.5)Pd30. Initial testing has indicated that this alloy, while having acceptable work characteristics, suffers from significant permanent deformation (or ratcheting) during thermal cycling under load. In an effort to overcome this deficiency, various solid-solution alloying and thermomechanical processing schemes were investigated. Solid-solution strengthening was achieved by substituting 5at% gold or platinum for palladium in Ni(19.5)Ti(50.5)Pd30, the so-called baseline alloy, to strengthen the martensite and austenite phases against slip processes and improve thermomechanical behavior. Tensile properties, work behavior, and dimensional stability during repeated thermal cycling under load for the ternary and quaternary alloys were compared. The relative difference in yield strength between the martensite and austenite phases and the dimensional stability of the alloy were improved by the quaternary additions, while work output was only minimally impacted. The three alloys were also thermomechanically processed by cycling repeatedly through the transformation range under a constant stress. This so-called training process dramatically improved the dimensional stability in these samples and also recovered the slight decrease in work output caused by quaternary alloying. An added benefit of the solid-solution strengthening was maintenance of enhanced dimensional stability of the trained material to higher temperatures compared to the baseline alloy, providing a greater measure of over-temperature capability.

  18. Cloud water composition during HCCT-2010: Scavenging efficiencies, solute concentrations, and droplet size dependence of inorganic ions and dissolved organic carbon

    NASA Astrophysics Data System (ADS)

    van Pinxteren, D.; Fomba, K. W.; Mertes, S.; Müller, K.; Spindler, G.; Schneider, J.; Lee, T.; Collett, J.; Herrmann, H.

    2015-09-01

    Cloud water samples were taken in September/October 2010 at Mt. Schmücke in a rural, forested area in Germany during the Lagrange-type Hill Cap Cloud Thuringia 2010 (HCCT-2010) cloud experiment. Besides bulk collectors, a 3-stage and a 5-stage collector were applied and samples were analysed for inorganic ions (SO42-, NO3-, NH4+, Cl-, Na+, Mg2+, Ca2+, K+), H2O2 (aq), S(IV), and dissolved organic carbon (DOC). Campaign volume-weighted mean concentrations were 191, 142, and 39 μmol L-1 for ammonium, nitrate, and sulfate, respectively, between 4 and 27 μmol L-1 for minor ions, 5.4 μmol L-1 for H2O2 (aq), 1.9 μmol L-1 for S(IV), and 3.9 mgC L-1 for DOC. The concentrations compare well to more recent European cloud water data from similar sites. On a mass basis, organic material (as DOC · 1.8) contributed 20-40 % (event means) to total solute concentrations and was found to have non-negligible impact on cloud water acidity. Relative standard deviations of major ions were 60-66 % for solute concentrations and 52-80 % for cloud water loadings (CWLs). Contrary to some earlier suggestions, the similar variability of solute concentrations and CWLs together with the results of back trajectory analysis and principal component analysis, suggests that concentrations in incoming air masses (i.e. air mass history), rather than cloud liquid water content (LWC) was the main factor controlling bulk solute concentrations at Mt. Schmücke. Droplet effective radius was found to be a somewhat better predictor for cloud water total ionic content (TIC) than LWC, even though no single explanatory variable can fully describe TIC (or solute concentration) variations in a simple functional relation due to the complex processes involved. Bulk concentrations typically agreed within a factor of 2 with co-located measurements of residual particle concentrations sampled by a counterflow virtual impactor (CV) and analysed by an aerosol mass spectrometer (AMS), with the deviations being mainly

  19. Cloud water composition during HCCT-2010: Scavenging efficiencies, solute concentrations, and droplet size dependence of inorganic ions and dissolved organic carbon

    NASA Astrophysics Data System (ADS)

    van Pinxteren, Dominik; Wadinga Fomba, Khanneh; Mertes, Stephan; Müller, Konrad; Spindler, Gerald; Schneider, Johannes; Lee, Taehyoung; Collett, Jeffrey L.; Herrmann, Hartmut

    2016-03-01

    Cloud water samples were taken in September/October 2010 at Mt. Schmücke in a rural, forested area in Germany during the Lagrange-type Hill Cap Cloud Thuringia 2010 (HCCT-2010) cloud experiment. Besides bulk collectors, a three-stage and a five-stage collector were applied and samples were analysed for inorganic ions (SO42-,NO3-, NH4+, Cl-, Na+, Mg2+, Ca2+, K+), H2O2 (aq), S(IV), and dissolved organic carbon (DOC). Campaign volume-weighted mean concentrations were 191, 142, and 39 µmol L-1 for ammonium, nitrate, and sulfate respectively, between 4 and 27 µmol L-1 for minor ions, 5.4 µmol L-1 for H2O2 (aq), 1.9 µmol L-1 for S(IV), and 3.9 mgC L-1 for DOC. The concentrations compare well to more recent European cloud water data from similar sites. On a mass basis, organic material (as DOC × 1.8) contributed 20-40 % (event means) to total solute concentrations and was found to have non-negligible impact on cloud water acidity. Relative standard deviations of major ions were 60-66 % for solute concentrations and 52-80 % for cloud water loadings (CWLs). The similar variability of solute concentrations and CWLs together with the results of back-trajectory analysis and principal component analysis, suggests that concentrations in incoming air masses (i.e. air mass history), rather than cloud liquid water content (LWC), were the main factor controlling bulk solute concentrations for the cloud studied. Droplet effective radius was found to be a somewhat better predictor for cloud water total ionic content (TIC) than LWC, even though no single explanatory variable can fully describe TIC (or solute concentration) variations in a simple functional relation due to the complex processes involved. Bulk concentrations typically agreed within a factor of 2 with co-located measurements of residual particle concentrations sampled by a counterflow virtual impactor (CVI) and analysed by an aerosol mass spectrometer (AMS), with the deviations being mainly caused by systematic

  20. Thermal activation mechanisms and Labusch-type strengthening analysis for a family of high-entropy and equiatomic solid-solution alloys

    DOE PAGES

    Wu, Zhenggang; Gao, Yanfei; Bei, Hongbin

    2016-11-01

    To understand the underlying strengthening mechanisms, thermal activation processes are investigated from stress-strain measurements with varying temperatures and strain rates for a family of equiatomic quinary, quaternary, ternary, and binary, face-center-cubic-structured, single phase solid-solution alloys, which are all subsystems of the FeNiCoCrMn high-entropy alloy. Our analysis suggests that the Labusch-type solution strengthening mechanism, rather than the lattice friction (or lattice resistance), governs the deformation behavior in equiatomic alloys. First, upon excluding the Hall-Petch effects, the activation volumes for these alloys are found to range from 10 to 1000 times the cubic power of Burgers vector, which are much larger thanmore » that required for kink pairs (i.e., the thermal activation process for the lattice resistance mechanism in body-center-cubic-structured metals). Second, the Labusch-type analysis for an N-element alloy is conducted by treating M-elements (M < N) as an effective medium and summing the strengthening contributions from the rest of N-M elements as individual solute species. For all equiatomic alloys investigated, a qualitative agreement exists between the measured strengthening effect and the Labusch strengthening factor from arbitrary M to N elements based on the lattice and modulus mismatches. Furthermore, the Labusch strengthening factor provides a practical critique to understand and design such compositionally complex but structurally simple alloys.« less

  1. Thermal activation mechanisms and Labusch-type strengthening analysis for a family of high-entropy and equiatomic solid-solution alloys

    SciTech Connect

    Wu, Zhenggang; Gao, Yanfei; Bei, Hongbin

    2016-11-01

    To understand the underlying strengthening mechanisms, thermal activation processes are investigated from stress-strain measurements with varying temperatures and strain rates for a family of equiatomic quinary, quaternary, ternary, and binary, face-center-cubic-structured, single phase solid-solution alloys, which are all subsystems of the FeNiCoCrMn high-entropy alloy. Our analysis suggests that the Labusch-type solution strengthening mechanism, rather than the lattice friction (or lattice resistance), governs the deformation behavior in equiatomic alloys. First, upon excluding the Hall-Petch effects, the activation volumes for these alloys are found to range from 10 to 1000 times the cubic power of Burgers vector, which are much larger than that required for kink pairs (i.e., the thermal activation process for the lattice resistance mechanism in body-center-cubic-structured metals). Second, the Labusch-type analysis for an N-element alloy is conducted by treating M-elements (M < N) as an effective medium and summing the strengthening contributions from the rest of N-M elements as individual solute species. For all equiatomic alloys investigated, a qualitative agreement exists between the measured strengthening effect and the Labusch strengthening factor from arbitrary M to N elements based on the lattice and modulus mismatches. Furthermore, the Labusch strengthening factor provides a practical critique to understand and design such compositionally complex but structurally simple alloys.

  2. Thermal activation mechanisms and Labusch-type strengthening analysis for a family of high-entropy and equiatomic solid-solution alloys

    DOE PAGES

    Wu, Zhenggang; Gao, Yanfei; Bei, Hongbin

    2016-11-01

    To understand the underlying strengthening mechanisms, thermal activation processes are investigated from stress-strain measurements with varying temperatures and strain rates for a family of equiatomic quinary, quaternary, ternary, and binary, face-center-cubic-structured, single phase solid-solution alloys, which are all subsystems of the FeNiCoCrMn high-entropy alloy. Our analysis suggests that the Labusch-type solution strengthening mechanism, rather than the lattice friction (or lattice resistance), governs the deformation behavior in equiatomic alloys. First, upon excluding the Hall-Petch effects, the activation volumes for these alloys are found to range from 10 to 1000 times the cubic power of Burgers vector, which are much larger thanmore » that required for kink pairs (i.e., the thermal activation process for the lattice resistance mechanism in body-center-cubic-structured metals). Second, the Labusch-type analysis for an N-element alloy is conducted by treating M-elements (M < N) as an effective medium and summing the strengthening contributions from the rest of N-M elements as individual solute species. For all equiatomic alloys investigated, a qualitative agreement exists between the measured strengthening effect and the Labusch strengthening factor from arbitrary M to N elements based on the lattice and modulus mismatches. Furthermore, the Labusch strengthening factor provides a practical critique to understand and design such compositionally complex but structurally simple alloys.« less

  3. Thermal activation mechanisms and Labusch-type strengthening analysis for a family of high-entropy and equiatomic solid-solution alloys

    SciTech Connect

    Wu, Zhenggang; Gao, Yanfei; Bei, Hongbin

    2016-11-01

    To understand the underlying strengthening mechanisms, thermal activation processes are investigated from stress-strain measurements with varying temperatures and strain rates for a family of equiatomic quinary, quaternary, ternary, and binary, face-center-cubic-structured, single phase solid-solution alloys, which are all subsystems of the FeNiCoCrMn high-entropy alloy. Our analysis suggests that the Labusch-type solution strengthening mechanism, rather than the lattice friction (or lattice resistance), governs the deformation behavior in equiatomic alloys. First, upon excluding the Hall-Petch effects, the activation volumes for these alloys are found to range from 10 to 1000 times the cubic power of Burgers vector, which are much larger than that required for kink pairs (i.e., the thermal activation process for the lattice resistance mechanism in body-center-cubic-structured metals). Second, the Labusch-type analysis for an N-element alloy is conducted by treating M-elements (M < N) as an effective medium and summing the strengthening contributions from the rest of N-M elements as individual solute species. For all equiatomic alloys investigated, a qualitative agreement exists between the measured strengthening effect and the Labusch strengthening factor from arbitrary M to N elements based on the lattice and modulus mismatches. Furthermore, the Labusch strengthening factor provides a practical critique to understand and design such compositionally complex but structurally simple alloys.

  4. Investigating the Temporal Effects of Metal-Based Coagulants to Remove Mercury from Solution in the Presence of Dissolved Organic Matter

    NASA Astrophysics Data System (ADS)

    Henneberry, Yumiko; Kraus, Tamara E. C.; Krabbenhoft, David P.; Horwath, William R.

    2016-01-01

    The presence of mercury (Hg), particularly methylmercury (MeHg), is a concern for both human and ecological health as MeHg is a neurotoxin and can bioaccumulate to lethal levels in upper trophic level organisms. Recent research has demonstrated that coagulation with metal-based salts can effectively remove both inorganic mercury (IHg) and MeHg from solution through association with dissolved organic matter (DOM) and subsequent flocculation and precipitation. In this study, we sought to further examine interactions between Hg and DOM and the resulting organo-metallic precipitate (floc) to assess if (1) newly added IHg could be removed to the same extent as ambient IHg or whether the association between IHg and DOM requires time, and (2) once formed, if the floc has the capacity to remove additional Hg from solution. Agricultural drainage water samples containing ambient concentrations of both DOM and IHg were spiked with a traceable amount of isotopically enriched IHg and dosed with ferric sulfate after 0, 1, 5, and 30 days. Both ambient and newly added IHg were removed within hours, with 69-79 % removed. To a separate sample set, isotopically enriched IHg was added to solution after floc had formed. Under those conditions, 81-95 % of newly added Hg was removed even at Hg concentrations 1000-fold higher than ambient levels. Results of this study indicate coagulation with ferric sulfate effectively removes both ambient and newly added IHg entering a system and suggests rapid association between IHg and DOM. This work also provides new information regarding the ability of floc to remove additional Hg from solution even after it has formed.

  5. Investigating the temporal effects of metal-based coagulants to remove mercury from solution in the presence of dissolved organic matter

    USGS Publications Warehouse

    Henneberry, Yumiko K.; Kraus, Tamara; Krabbenhoft, David P.; Horwath, William R.

    2015-01-01

    The presence of mercury (Hg), particularly methylmercury (MeHg), is a concern for both human and ecological health as MeHg is a neurotoxin and can bioaccumulate to lethal levels in upper trophic level organisms. Recent research has demonstrated that coagulation with metal-based salts can effectively remove both inorganic mercury (IHg) and MeHg from solution through association with dissolved organic matter (DOM) and subsequent flocculation and precipitation. In this study, we sought to further examine interactions between Hg and DOM and the resulting organo-metallic precipitate (floc) to assess if (1) newly added IHg could be removed to the same extent as ambient IHg or whether the association between IHg and DOM requires time, and (2) once formed, if the floc has the capacity to remove additional Hg from solution. Agricultural drainage water samples containing ambient concentrations of both DOM and IHg were spiked with a traceable amount of isotopically enriched IHg and dosed with ferric sulfate after 0, 1, 5, and 30 days. Both ambient and newly added IHg were removed within hours, with 69–79 % removed. To a separate sample set, isotopically enriched IHg was added to solution after floc had formed. Under those conditions, 81–95 % of newly added Hg was removed even at Hg concentrations 1000-fold higher than ambient levels. Results of this study indicate coagulation with ferric sulfate effectively removes both ambient and newly added IHg entering a system and suggests rapid association between IHg and DOM. This work also provides new information regarding the ability of floc to remove additional Hg from solution even after it has formed.

  6. Creation of Novel Solid-Solution Alloy Nanoparticles on the Basis of Density-of-States Engineering by Interelement Fusion.

    PubMed

    Kobayashi, Hirokazu; Kusada, Kohei; Kitagawa, Hiroshi

    2015-06-16

    Currently 118 known elements are represented in the periodic table. Of these 118 elements, only about 80 elements are stable, nonradioactive, and widely available for our society. From the viewpoint of the "elements strategy", we need to make full use of the 80 elements to bring out their latent ability and create innovative materials. Furthermore, there is a strong demand that the use of rare or toxic elements be reduced or replaced while their important properties are retained. Advanced science and technology could create higher-performance materials even while replacing or reducing minor or harmful elements through the combination of more abundant elements. The properties of elements are correlated directly with their electronic states. In a solid, the magnitude of the density of states (DOS) at the Fermi level affects the physical and chemical properties. In the present age, more attention has been paid to improving the properties of materials by means of alloying elements. In particular, the solid-solution-type alloy is advantageous because the properties can be continuously controlled by tuning the compositions and/or combinations of the constituent elements. However, the majority of bulk alloys are of the phase-separated type under ambient conditions, where constituent elements are immiscible with each other. To overcome the challenge of the bulk-phase metallurgical aspects, we have focused on the nanosize effect and developed methods involving "nonequilibrium synthesis" or "a process of hydrogen absorption/desorption". We propose a new concept of "density-of-states engineering" for the design of materials having the most desirable and suitable properties by means of "interelement fusion". In this Account, we describe novel solid-solution alloys of Pd-Pt, Ag-Rh, and Pd-Ru systems in which the constituent elements are immiscible in the bulk state. The homogeneous solid-solution alloys of Pd and Pt were created from Pd core/Pt shell nanoparticles using a

  7. Influence of dissolved organic matter and oil on the biosorption of BTEX by macroalgae in single and multi-solute systems.

    PubMed

    Rodriguez-Hernandez, Mayra Cecilia; Flores-Chaparro, Carlos E; Rangel-Mendez, Jose Rene

    2017-07-18

    The effect of dissolved organic matter (DOM) and oil on the removal of the water-soluble compounds benzene, toluene, ethylbenzene, and xylene isomers (BTEX) by two low-cost biosorbents Macrocystis pyrifera and Ulva expansa) was evaluated. DOM decreased the adsorption capacity of toluene, ethylbenzene, and xylenes of the two biosorbents. In contrast, the removal of benzene increased under the same conditions in single and multi-solute systems: this effect was dominant in U. expansa biomass treatments. In the presence of DOM and oil in solutions, the removal of BTEX notoriously increased, being oil that contributed the most. Solubility and hydrophobicity of pollutants played a key role in the adsorption process. The attractions between BTEX molecules and biosorbents were governed by π-π and hydrophobic interactions. Affinities of biosorbents for BTEX were mainly in the order of X > E > T > B. The Langmuir and Sips equations adjusted the adsorption isotherms for BTEX biosorption in deionized and natural water samples, but in the case of oily systems, the Freundlich equation seemed to have a better fit. The biosorption processes followed a pseudo-second-order rate in all the cases.

  8. Extremely high-rate, uniform dissolution of alloy C-22 in anhydrous organic solutions at room temperature

    SciTech Connect

    Schindelholz, Eric J.; Christie, Michael A.; Allwein, Shawn P.; Kelly, Robert G.

    2016-06-21

    During routine pharmaceutical development and scale-up work, severe corrosion of a Hastelloy Alloy C-22 filter dryer was observed after single, short (several hours) contact with the product slurry at room temperature. Initial investigations showed that the presence of both 2,3-dichloro-5,6-dicyano-1,4-benzoquinone (DDQ) and HCl was sufficient in an acetonitrile solution to cause rapid corrosion of C-22. More detailed mass loss studies showed initial corrosion rates exceeding25 mm/year that then decreased over several hours to steady state rates of 3-5 mm/year. The corrosion was highly uniform. Electrochemical measurements demonstrated that although C-22 is spontaneously passive in acetonitrile solution, the presence of HCl leads to the development of a transpassive region. Furthermore, DDQ is a sufficiently strong oxidizer, particularly in acidic solutions, to polarize the C-22 well into the transpassive region, leading to the observed high corrosion rates.

  9. Extremely high-rate, uniform dissolution of alloy C-22 in anhydrous organic solutions at room temperature

    SciTech Connect

    Schindelholz, Eric J.; Christie, Michael A.; Allwein, Shawn P.; Kelly, Robert G.

    2016-06-21

    During routine pharmaceutical development and scale-up work, severe corrosion of a Hastelloy Alloy C-22 filter dryer was observed after single, short (several hours) contact with the product slurry at room temperature. Initial investigations showed that the presence of both 2,3-dichloro-5,6-dicyano-1,4-benzoquinone (DDQ) and HCl was sufficient in an acetonitrile solution to cause rapid corrosion of C-22. More detailed mass loss studies showed initial corrosion rates exceeding25 mm/year that then decreased over several hours to steady state rates of 3-5 mm/year. The corrosion was highly uniform. Electrochemical measurements demonstrated that although C-22 is spontaneously passive in acetonitrile solution, the presence of HCl leads to the development of a transpassive region. Furthermore, DDQ is a sufficiently strong oxidizer, particularly in acidic solutions, to polarize the C-22 well into the transpassive region, leading to the observed high corrosion rates.

  10. Mechanisms controlling the production and transport of methane, carbon dioxide, and dissolved solutes within a boreal peatland. Progress report, January 15, 1991--July 14, 1992

    SciTech Connect

    Siegel, D.I.

    1992-04-09

    Peatlands are one of the most important terrestrial reservoirs in the global cycle for carbon, and are a major source for atmospheric methane. However, little is known about the dynamics of these carbon reservoirs or their feedback mechanisms with the pool of atmospheric CO{sub 2} during the Holocene. Specifically, it is unknown whether large peat basins are sources, sinks, or steady-state reservoirs for the global carbon cycle. In particular, the production and transport of methane, carbon dioxide, and dissolved organic carbon form the deeper portions of these peatlands is unknown. Our DOE research program is to conduct an integrated ecologic and hydrogeochemical study of the Glacial Lake Agassiz peatlands (northern Minnesota) to better understand the carbon dynamics in globally significant peat basins. Specifically, our study will provide local and regional data on (1), rates of carbon accumulation and loss and fluxes of methane in the peat profiles; (2) the physical and botanical factors controlling the production of methane and carbon dioxide in the wetland; and (3) the role of hydrogeologic processes in controlling the fluxes of gases and solutes through the peat. We intend to use computer simulation models, calibrated to field data, to scale-up from local to regional estimates of methane and carbon dioxide within the basin. How gases and dissolved organic carbon escapes form peatlands in unknown. It has been suggested that the concentrations of methane produced in the upper peat are sufficient to produce diffusion gradients towards the surface. Alternatively, gas may move through the peat profile by groundwater advection.

  11. Process for alloying uranium and niobium

    DOEpatents

    Holcombe, Cressie E.; Northcutt, Jr., Walter G.; Masters, David R.; Chapman, Lloyd R.

    1991-01-01

    Alloys such as U-6Nb are prepared by forming a stacked sandwich array of uraniun sheets and niobium powder disposed in layers between the sheets, heating the array in a vacuum induction melting furnace to a temperature such as to melt the uranium, holding the resulting mixture at a temperature above the melting point of uranium until the niobium dissolves in the uranium, and casting the uranium-niobium solution. Compositional uniformity in the alloy product is enabled by use of the sandwich structure of uranium sheets and niobium powder.

  12. Development of a novel high-entropy alloy with eminent efficiency of degrading azo dye solutions

    PubMed Central

    Lv, Z. Y.; Liu, X. J.; Jia, B.; Wang, H.; Wu, Y.; Lu, Z. P.

    2016-01-01

    In addition to its scientific importance, the degradation of azo dyes is of practical significance from the perspective of environmental protection. Although encouraging progress has been made on developing degradation approaches and materials, it is still challenging to fully resolve this long-standing problem. Herein, we report that high entropy alloys, which have been emerging as a new class of metallic materials in the last decade, have excellent performance in degradation of azo dyes. In particular, the newly developed AlCoCrTiZn high-entropy alloy synthesized by mechanical alloying exhibits a prominent efficiency in degradation of the azo dye (Direct Blue 6: DB6), as high as that of the best metallic glass reported so far. The newly developed AlCoCrTiZn HEA powder has low activation energy barrier, i.e., 30 kJ/mol, for the degrading reaction and thus make the occurrence of reaction easier as compared with other materials such as the glassy Fe-based powders. The excellent capability of our high-entropy alloys in degrading azo dye is attributed to their unique atomic structure with severe lattice distortion, chemical composition effect, residual stress and high specific surface area. Our findings have important implications in developing novel high-entropy alloys for functional applications as catalyst materials. PMID:27677462

  13. Development of a novel high-entropy alloy with eminent efficiency of degrading azo dye solutions.

    PubMed

    Lv, Z Y; Liu, X J; Jia, B; Wang, H; Wu, Y; Lu, Z P

    2016-09-28

    In addition to its scientific importance, the degradation of azo dyes is of practical significance from the perspective of environmental protection. Although encouraging progress has been made on developing degradation approaches and materials, it is still challenging to fully resolve this long-standing problem. Herein, we report that high entropy alloys, which have been emerging as a new class of metallic materials in the last decade, have excellent performance in degradation of azo dyes. In particular, the newly developed AlCoCrTiZn high-entropy alloy synthesized by mechanical alloying exhibits a prominent efficiency in degradation of the azo dye (Direct Blue 6: DB6), as high as that of the best metallic glass reported so far. The newly developed AlCoCrTiZn HEA powder has low activation energy barrier, i.e., 30 kJ/mol, for the degrading reaction and thus make the occurrence of reaction easier as compared with other materials such as the glassy Fe-based powders. The excellent capability of our high-entropy alloys in degrading azo dye is attributed to their unique atomic structure with severe lattice distortion, chemical composition effect, residual stress and high specific surface area. Our findings have important implications in developing novel high-entropy alloys for functional applications as catalyst materials.

  14. Development of a novel high-entropy alloy with eminent efficiency of degrading azo dye solutions

    NASA Astrophysics Data System (ADS)

    Lv, Z. Y.; Liu, X. J.; Jia, B.; Wang, H.; Wu, Y.; Lu, Z. P.

    2016-09-01

    In addition to its scientific importance, the degradation of azo dyes is of practical significance from the perspective of environmental protection. Although encouraging progress has been made on developing degradation approaches and materials, it is still challenging to fully resolve this long-standing problem. Herein, we report that high entropy alloys, which have been emerging as a new class of metallic materials in the last decade, have excellent performance in degradation of azo dyes. In particular, the newly developed AlCoCrTiZn high-entropy alloy synthesized by mechanical alloying exhibits a prominent efficiency in degradation of the azo dye (Direct Blue 6: DB6), as high as that of the best metallic glass reported so far. The newly developed AlCoCrTiZn HEA powder has low activation energy barrier, i.e., 30 kJ/mol, for the degrading reaction and thus make the occurrence of reaction easier as compared with other materials such as the glassy Fe-based powders. The excellent capability of our high-entropy alloys in degrading azo dye is attributed to their unique atomic structure with severe lattice distortion, chemical composition effect, residual stress and high specific surface area. Our findings have important implications in developing novel high-entropy alloys for functional applications as catalyst materials.

  15. Method for low temperature preparation of a noble metal alloy

    DOEpatents

    Even, Jr., William R.

    2002-01-01

    A method for producing fine, essentially contamination free, noble metal alloys is disclosed. The alloys comprise particles in a size range of 5 to 500 nm. The method comprises 1. A method for preparing a noble metal alloy at low temperature, the method comprising the steps of forming solution of organometallic compounds by dissolving the compounds into a quantity of a compatible solvent medium capable of solvating the organometallic, mixing a portion of each solution to provide a desired molarity ratio of ions in the mixed solution, adding a support material, rapidly quenching droplets of the mixed solution to initiate a solute-solvent phase separation as the solvent freezes, removing said liquid cryogen, collecting and freezing drying the frozen droplets to produce a dry powder, and finally reducing the powder to a metal by flowing dry hydrogen over the powder while warming the powder to a temperature of about 150.degree. C.

  16. Extreme Chemical Disorder and the Electrical Transport Properties of Concentrated Solid Solution Alloys: From Binaries to High Entropy Alloys Replace this text with your abstract title

    NASA Astrophysics Data System (ADS)

    Stocks, G. Malcolm; Samolyuk, German; Khan, Suffian; Daene, Markus; Wimmer, Sebastian; Sales, Brian; Bei, Hongbin; Jin, Ke

    We present the results of experimental and theoretical studies of electrical transport properties of a family of 2, 3, 4 and 5-component concentrated solid solution alloys (CSA) comprising subsets of the 3d- and 4d-transition metal elements Cr, Mn, Fe, Co, Ni and Pd. Many of this family of CSA show unusual mechanical, magnetic and transport properties as well as indications of increased radiation resistance that are clearly related to the underlying chemical disorder. Here we show the results of calculations of the electrical transport properties that are based on the ab initio Korringa-Kohn-Rostoker coherent-potential-approximation (KKR-CPA) method for treating the effect of substitutional disorder, and necessary configurational averaging, on the underlying electronic structure. We compare calculated residual (T =0K) resistivities to corresponding experimental measurements and relate the variations in residual resistivity, which span almost two orders of magnitude, to the underlying electron structure.

  17. Preparation of conversion coating on Ti-6Al-4V alloy in mixed solution of phytic acid and ammonium fluoride through chemical modification

    NASA Astrophysics Data System (ADS)

    Li, Lanlan; He, Jian; Yang, Xu

    2016-05-01

    Conversion coatings on Ti-6Al-4V alloy was prepared through chemical modification in phytic acid and ammonium fluoride mixed solution. The influences of pH, time and the composition of solution on the microstructure of alloy surface were investigated. Scanning electron microscopy was used to observe the microstructure. The chemical composition of alloy surface before and after modification was investigated by energy dispersive X-ray spectroscopy. The results indicated that a conversion coating could be formed on the Ti-6Al-4V alloy in a mixed solution of phytic acid and ammonium fluoride, the growth and microstructure of the conversion coatings were critically dependent on the pH, time and concentration of phytic acid and ammonium fluoride. In 100 mg/ml phytic acid containing 125 mg/ml ammonium fluoride solution with a pH of 6, a compact conversion coating with the thickness of about 4.7 μm formed after 30 min immersion on Ti-6Al-4V alloy surface. The preliminary evaluation of bioactivity of conversion coating was performed by in vitro cell experiments. The results showed that this chemical modification method is a promising surface modification technique for Ti-6Al-4V alloy inplants.

  18. Preparation and characterization of Y-Fe alloy nanowires by template-assisted electrodeposition from aqueous solution

    NASA Astrophysics Data System (ADS)

    Wang, XiaoChao; Han, Li; Zhang, YuanYuan; Xue, ShouHong

    2016-03-01

    In this study, a method was proposed for the preparation of Y-Fe alloy nanowires by PC membrane template-assisted electrodeposition from aqueous solution. Citric acid acted as complexing agent was used into the solution to fabricate Y-Fe alloy nanowires. The electrolyte solution consisted of 5 g L-1 YCl3, 12.5 g L-1 FeSO·6H2O, different concentrations of citric acid , 25 g L-1 boric acid in deionized water. The energy dispersive spectroscopy (EDS) found that the content of Y in the nanowires can be controlled by citric acid concentration and the current intensity, and the content of Y could reach up to 33.16 wt%. Scanning electron microscopy (SEM), BET specific surface area (BET), and X-ray diffraction (XRD) showed that there was a shift in the structure of nanowires from semicrystalline to amorphous due to the change of Y content, and their shapes were approximately 100 nm in diameter and 6 μm in length; the surface areas of nanowires were about 3.97 m2/g. Fourier transform infrared (FTIR) spectroscopy, UV-Vis diffuse reflectance spectroscopy, and X-ray photoelectron spectroscopy (XPS) indicated the formation of Y-Fe alloy, Y2O3 and Fe2O3 existed in the outer layer of nanowires. The magnetic field applied both parallel and perpendicular to the nanowires by alternating gradient magnetometer (AGM) showed small magnetic anisotropy and low coercivity with easy axis of magnetization perpendicular to the nanowires. In addition, the magneto-optic Kerr effect (MOKE) was investigated, and a Kerr rotation angle of 29 mdeg was obtained.

  19. Solid solution strengthened duct and cladding alloy D9-B1

    DOEpatents

    Korenko, Michael K.

    1983-01-01

    A modified AISI type 316 stainless steel is described for use in an atmosphere where the alloy will be subject to neutron irradiation. The alloy is characterized by its phase stability in both the annealed as well as cold work condition and above all by its superior resistance to radiation induced swelling. Graphical data is included to demonstrate the superior swelling resistance of the alloy which contains from about 0.5% to 2.2% manganese, from about 0.7% to about 1.1% silicon, from about 12.5% to 14% chromium, from about 14.5% to about 16.5% nickel, from about 1.2% to about 1.6% molybdenum, from 0.15% to 0.30% titanium, from 0.02% to 0.08% zirconium, and the balance iron with incidental impurities.

  20. Electrochemical behavior of near-beta titanium biomedical alloys in phosphate buffer saline solution.

    PubMed

    Dalmau, A; Guiñón Pina, V; Devesa, F; Amigó, V; Igual Muñoz, A

    2015-03-01

    The electrochemical behavior of three different near-β titanium alloys (composed by Ti, Nb and Sn) obtained by powder metallurgy for biomedical applications has been investigated. Different electrochemical and microscopy techniques were used to study the influence of the chemical composition (Sn content) and the applied potential on the microstructure and the corrosion mechanisms of those titanium alloys. The addition of Sn below 4wt.% to the titanium powder improves the microstructural homogeneity and generates an alloy with high corrosion resistance with low elastic modulus, being more suitable as a biomaterial. When the Sn content is above 4%, the corrosion resistance considerably decreases by increasing the passive dissolution rate; this effect is enhanced with the applied potential. Copyright © 2014 Elsevier B.V. All rights reserved.

  1. Laboratory persistence in soil of thiacloprid, pendimethalin and fenarimol incubated with treated wastewater and dissolved organic matter solutions. Contribution of soil biota.

    PubMed

    Rodríguez-Liébana, José Antonio; ElGouzi, Siham; Peña, Aránzazu

    2017-08-01

    Reutilization of treated wastewater (TWW) in agriculture has continued to grow, especially in areas prone to frequent drought periods. One of the major aspects derived from this practice is the addition of important amounts of organic carbon (OC) that could interfere with the fate of organic contaminants in soils. This study has evaluated the impact of irrigation with a secondary TWW and dissolved OC (DOC) solutions from sewage sludge in the dissipation of thiacloprid (THC), pendimethalin (PDM) and fenarimol (FEN) in an OC-poor agricultural soil under laboratory conditions. The effect on soil microbial activity was also assessed through the measurement of dehydrogenase activity. Biotic processes were the main responsible for the degradation of the three compounds. Results showed that while THC was rapidly degraded (DT50 ≤ 5.5 d), PDM and FEN were moderately persistent in soil (DT50 ≥ 93 d). Incubation with TWW did not modify the decay rate of the three pesticides, but initially inhibited soil biota. Solutions of DOC did not alter the dissipation of FEN, but contrasting effects were observed for THC and PDM. Low DOC concentrations (30 mg L(-1)) accelerated THC disappearance, a fact explained by stimulation of endogenous biota rather than by the presence of exogenous microorganisms from the solution. On the other hand, high DOC concentrations (300 mg L(-1)) had more influence on the activity of microorganisms at longer times, and showed a trend to enhance the disappearance of the moderately persistent PDM. Copyright © 2017 Elsevier Ltd. All rights reserved.

  2. Structural evolution of aqueous NaCl solutions dissolved in supercritical carbon dioxide under isobaric heating by mid and near infrared spectroscopy.

    PubMed

    Oparin, R; Tassaing, T; Danten, Y; Besnard, M

    2005-03-01

    The local order in aqueous NaCl solutions diluted in supercritical carbon dioxide at constant pressure as a function of NaCl concentration and temperature has been investigated using near and mid infrared absorption spectroscopy. The near IR results have allowed us to estimate the water concentration in CO(2) rich phase, whereas the state of water aggregation in CO(2) phase was investigated using mid IR spectroscopy. The analysis of the band shape variations of the OD stretching mode of HOD led us to conclude that below 100 degrees C, water molecules dissolved in CO(2) exist only under their monomeric form, whatever the salt concentration is, whereas hydrogen-bonded species, namely, dimers start to appear at higher temperatures. Larger aggregates have a negligible concentration in the range of temperature-pressure investigated. Using near and mid infrared data, we have calculated the concentrations of water species in the CO(2) phase. Upon heating, it was found that the concentration of dimers considerably increases at the expense of the monomers and only dimers are detected in carbon dioxide at highest temperatures. Changing the salt concentration affects significantly the concentration of monomers and decreases strongly the dimers population as the solution becomes progressively saturated in salt. In the saturated solution, at 340 degrees C, the dimer concentration is at least two times smaller than in the binary water-CO(2) mixture. These findings are in qualitative agreement with existing thermodynamics data showing that addition of NaCl to the binary H(2)O-CO(2) system shifts the range of partial miscibility of water and CO(2) towards higher pressure and temperature.

  3. The Solidification Velocity of Undercooled Nickel and Titanium Alloys with Dilute Solute

    NASA Technical Reports Server (NTRS)

    Algoso, Paul R.; Altgilbers, A. S.; Hofmeister, William H.; Bayuzick, Robert J.

    2003-01-01

    The study of solidification velocity is important for two reasons. First, understanding the manner in which the degree of undercooling of the liquid and solidification velocity affect the microstructure of the solid is fundamental. Second, there is disagreement between theoretical predictions of the relationship between undercooling and solidification velocity and experimental results. Thus, the objective of this research is to accurately and systematically quantify the solidification velocity as a function of undercooling for dilute nickel-and titanium-based alloys. The alloys chosen for study cover a wide range of equilibrium partition coefficients, and the results are compared to current theory.

  4. Pressure-induced fcc to hcp phase transition in Ni-based high entropy solid solution alloys

    DOE PAGES

    Zhang, Fuxiang; Zhao, Shijun; Jin, Ke; ...

    2017-01-04

    In this research, pressure-induced phase transition from the fcc to a hexagonal close-packed (hcp) structure wasfound in NiCoCrFe solid solution alloy starting at 13.5 GPa. The phase transition is very sluggish and the transition did not complete at ~ 40 GPa. The hcp structure is quenchable to ambient pressure. Only a very small amount (<5%) of hcp phase was found in the isostructural NiCoCr ternary alloy up to the pressure of 45 GPa and no obvious hcp phase was found in NiCoCrFePd system till to 74 GPa. Ab initio Gibbs free energy calculations indicated the energy differences between the fccmore » and the hcp phases for the three alloys are very small, but they are sensitive to temperature. Finally, the critical transition pressure in NiCoCrFe varies from 1 GPa at room temperature to 6 GPa at 500 K.« less

  5. Preferential diffusion in concentrated solid solution alloys: NiFe, NiCo and NiCoCr

    DOE PAGES

    Zhao, Shijun; Osetsky, Yuri; Zhang, Yanwen

    2017-02-13

    In single-phase concentrated solid-solution alloys (CSAs), including high entropy alloys (HEAs), remarkable mechanical properties are exhibited, as well as extraordinary corrosion and radiation resistance compared to pure metals and dilute alloys. But, the mechanisms responsible for these properties are unknown in many cases. In this work, we employ ab initio molecular dynamics based on density functional theory to study the diffusion of interstitial atoms in Ni and Ni-based face-centered cubic CSAs including NiFe, NiCo and NiCoCr. We model the defect trajectories over >100 ps and estimate tracer diffusion coefficients, correlation factors and activation energies. Furthermore, we found that the diffusionmore » mass transport in CSAs is not only slower than that in pure components, i.e. sluggish diffusion, but also chemically non-homogeneous. The results obtained here can be used in understanding and predicting the atomic segregation and phase separation in CSAs under irradiation conditions.« less

  6. High-throughput combinatorial study of the effect of M site alloying on the solid solution behavior of M2AlC MAX phases

    NASA Astrophysics Data System (ADS)

    Talapatra, Anjana; Duong, T.; Son, W.; Gao, H.; Radovic, M.; Arróyave, R.

    2016-09-01

    In this work, a systematic investigation of the alloying behavior on the M sublattice of M2AlC , where M is Ti, V, Zr, and Hf with elements in the first transition metal row as well as Ca and Sc is carried out via a combination of alloy theoretic approaches and density functional theory for 41 alloy systems. The cluster expansion formalism is used to explore the configurational space in ternary MAX phases. On the basis of their solid-solution behavior, the alloys are classified into three regimes: phase separation, weak ordering, and strong ordering. Observed trends are investigated in terms of indicators at the electronic and structural levels. For the systems showing ordering, the ordered structures are identified and their structural and electronic properties are investigated. The likelihood of some of the systems to exist as solid solutions at finite temperature is discussed.

  7. Interaction between solute atoms and radiation defects in Fe-Ni-Si and Fe-Mn-Si alloys under irradiation with proton ions at low-temperature

    NASA Astrophysics Data System (ADS)

    Murakami, Kenta; Iwai, Takeo; Abe, Hiroaki; Sekimura, Naoto

    2016-12-01

    Isochronal annealing followed by residual resistivity measurements at 12 K was performed in Fe-0.6Ni-0.6Si and Fe-1.5Mn-0.6Si alloys irradiated with 1 MeV proton ions below 70 K, and recovery stages were compared with those of Fe-0.6Ni and Fe-1.5Mn. The effects of silicon addition in the Fe-Ni alloy was observed as the appearance of a new recovery stage at 282-372 K, presumably corresponding to clustering of solute atoms in matrix, and as a change in mixed dumbbell migration at 122-142 K. Silicon addition mitigated the manganese effect in Fe-Mn alloy that is obstructing the recovery of radiation defects. Reduction of resistivity in Fe-Mn-Si alloy also suggested formation of small solute atom clusters.

  8. Enhanced selectivity for the electrochemical reduction of CO2 to alcohols in aqueous solution with nanostructured Cu-Au alloy as catalyst

    NASA Astrophysics Data System (ADS)

    Jia, Falong; Yu, Xinxing; Zhang, Lizhi

    2014-04-01

    Electrochemical reduction of CO2 in an aqueous 0.5 M KHCO3 solution is studied by use of novel nanostructured Cu-Au alloys, which are prepared through electrochemical deposition with a nanoporous Cu film (NCF) as template. Linear voltammetry results show that the as-synthesized Cu-Au alloys exhibit obvious catalysis towards electrochemical reduction of CO2. Further analysis of products reveals that faradic efficiencies of alcohols (methanol and ethanol) are greatly dependent on the nanostructures and compositions of Cu-Au alloys. It is expected that this work could provide new insight into the development of powerful electrocatalysts for reduction of CO2 to alcohols.

  9. Comparative analysis of the reactivity of nickel and a Ni-Re (10 wt %) alloy during direct current polarization in sulfuric acid solutions

    NASA Astrophysics Data System (ADS)

    Bryukvin, V. A.; Skryleva, E. A.; Levchuk, O. M.; Tsybin, O. I.; Bol'shikh, A. O.; Kuznetsova, O. G.

    2016-11-01

    A comparative analysis of the reactivity of nickel and its alloy with rhenium during their direct current polarization in sulfuric acid solutions (50-150 g/L, 25-60°C) is carried out. The regions of anodic potentials of their active dissolution and passivation are determined on the basis of the analysis results. The chemical compositions of the passivation films of electrode polarization are determined by X-ray photoelectron spectroscopy. The mechanism of film formation is established. The influence of the depolarizing ability of rhenium in the alloy composition on the depassivation of the alloy is revealed and evaluated.

  10. Experimental Determination of CO_2 Diffusion Coefficient in Aqueous Solutions Under Pressure via Raman Spectroscopy at Room Temparature: Impact of Salinity (NaCl) on Dissolved CO_2 Diffusivity

    NASA Astrophysics Data System (ADS)

    Belgodere, C.; Dubessy, J.; Sterpenich, J.; Pironon, J.; Vautrin, D.; Caumon, M. C.; Robert, P.; Randi, A.; Birat, J. P.

    2014-06-01

    Diffusion coefficient of dissolved CO_ at 40 bar pressure and 21 ± 1°C was calculated using Raman spectroscopy of aqueous solutions, from 0 to 6 molNaCl . Kg^-1 H_2O, loaded in a High-Pressure Optical Cell.

  11. Solute transport during the cyclic oxidation of Ni-Cr-Al alloys. M.S. Thesis

    NASA Technical Reports Server (NTRS)

    Nesbitt, J. A.

    1982-01-01

    Important requirements for protective coatings of Ni-Cr-Al alloys for gas turbine superalloys are resistance to oxidation accompanied by thermal cycling, resistance to thermal fatigue cracking. The resistance to oxidation accompanied by thermal cycling is discussed. The resistance to thermal fatigue cracking is also considered.

  12. Purification of uranium alloys by differential solubility of oxides and production of purified fuel precursors

    DOEpatents

    McLean, II, William; Miller, Philip E.

    1997-01-01

    A method for purifying metallic alloys of uranium for use as nuclear reactor fuels in which the metal alloy is first converted to an oxide and then dissolved in nitric acid. Initial removal of metal oxide impurities not soluble in nitric acid is accomplished by filtration or other physical means. Further purification can be accomplished by carbonate leaching of uranyl ions from the partially purified solution or using traditional methods such as solvent extraction.

  13. Purification of uranium alloys by differential solubility of oxides and production of purified fuel precursors

    DOEpatents

    McLean, W. II; Miller, P.E.

    1997-12-16

    A method is described for purifying metallic alloys of uranium for use as nuclear reactor fuels in which the metal alloy is first converted to an oxide and then dissolved in nitric acid. Initial removal of metal oxide impurities not soluble in nitric acid is accomplished by filtration or other physical means. Further purification can be accomplished by carbonate leaching of uranyl ions from the partially purified solution or using traditional methods such as solvent extraction. 3 figs.

  14. REMOVAL OF CHLORIDE FROM AQUEOUS SOLUTIONS

    DOEpatents

    Hyman, M.L.; Savolainen, J.E.

    1960-01-01

    A method is given for dissolving reactor fuel elements in which the uranium is associated with a relatively inert chromium-containing alloy such as stainless steel. An aqueous mixture of acids comprising 2 to 2.5 molar hydrochloric acid and 4 to 8 molar nitric acid is employed in dissolving the fuel element. In order io reduce corrosion in subsequent processing of the resulting solution, chloride values are removed from the solution by contacting it with concentrated nitric acid at an elevated temperature.

  15. Effect of Pre-strain on the Solute Clustering, Mechanical Properties, and Work-Hardening of a Naturally Aged Al-Cu-Mg Alloy

    NASA Astrophysics Data System (ADS)

    Shao, D.; Zhang, P.; Zhang, J. Y.; Liu, G.; Wang, R. H.; Liu, W. Q.; Sha, G.; Sun, J.

    2017-09-01

    The effect of pre-strain on the solute clustering, mechanical properties, and work-hardening of a naturally aged Al-Cu-Mg alloy was comprehensively investigated using a three-dimensional atom probe, electrical resistivity, and hardness measurements. The pre-strain promoted the rapid formation of solute clusters but suppressed the growth of solute clusters during prolonged aging. An increase in pre-strain caused a decrease in the saturated number density of solute clusters, leading to a reduction in cluster strengthening. By taking into account the coupling effect of solute clusters and pre-existing dislocations, models were proposed to address the yield strength and work-hardening behaviors of the Al-Cu-Mg alloy, respectively. It reveals that the solute-cluster strengthening is comparable to dislocation strengthening in the naturally aged alloy. However, the work hardening is not significantly affected by the presence of the solute clusters. The findings reported in this paper will be helpful for the development of a naturally aged Al-Cu-Mg alloy with improved performance by controlling the pre-strain.

  16. Effect of Pre-strain on the Solute Clustering, Mechanical Properties, and Work-Hardening of a Naturally Aged Al-Cu-Mg Alloy

    NASA Astrophysics Data System (ADS)

    Shao, D.; Zhang, P.; Zhang, J. Y.; Liu, G.; Wang, R. H.; Liu, W. Q.; Sha, G.; Sun, J.

    2017-07-01

    The effect of pre-strain on the solute clustering, mechanical properties, and work-hardening of a naturally aged Al-Cu-Mg alloy was comprehensively investigated using a three-dimensional atom probe, electrical resistivity, and hardness measurements. The pre-strain promoted the rapid formation of solute clusters but suppressed the growth of solute clusters during prolonged aging. An increase in pre-strain caused a decrease in the saturated number density of solute clusters, leading to a reduction in cluster strengthening. By taking into account the coupling effect of solute clusters and pre-existing dislocations, models were proposed to address the yield strength and work-hardening behaviors of the Al-Cu-Mg alloy, respectively. It reveals that the solute-cluster strengthening is comparable to dislocation strengthening in the naturally aged alloy. However, the work hardening is not significantly affected by the presence of the solute clusters. The findings reported in this paper will be helpful for the development of a naturally aged Al-Cu-Mg alloy with improved performance by controlling the pre-strain.

  17. Dispersoid reinforced alloy powder and method of making

    DOEpatents

    Anderson, Iver E; Terpstra, Robert L

    2014-10-21

    A method of making dispersion-strengthened alloy particles involves melting an alloy having a corrosion and/or oxidation resistance-imparting alloying element, a dispersoid-forming element, and a matrix metal wherein the dispersoid-forming element exhibits a greater tendency to react with a reactive species acquired from an atomizing gas than does the alloying element. The melted alloy is atomized with the atomizing gas including the reactive species to form atomized particles so that the reactive species is (a) dissolved in solid solution to a depth below the surface of atomized particles and/or (b) reacted with the dispersoid-forming element to form dispersoids in the atomized particles to a depth below the surface of said atomized particles. Bodies made from the dispersion strengthened solidified particles exhibit enhanced fatigue and creep resistance and reduced wear as well as enhanced corrosion and/or oxidation resistance at high temperatures.

  18. Time series models for prediction the total and dissolved heavy metals concentration in road runoff and soil solution of roadside embankments

    NASA Astrophysics Data System (ADS)

    Aljoumani, Basem; Kluge, Björn; sanchez, Josep; Wessolek, Gerd

    2017-04-01

    Highways and main roads are potential sources of contamination for the surrounding environment. High traffic rates result in elevated heavy metal concentrations in road runoff, soil and water seepage, which has attracted much attention in the recent past. Prediction of heavy metals transfer near the roadside into deeper soil layers are very important to prevent the groundwater pollution. This study was carried out on data of a number of lysimeters which were installed along the A115 highway (Germany) with a mean daily traffic of 90.000 vehicles per day. Three polyethylene (PE) lysimeters were installed at the A115 highway. They have the following dimensions: length 150 cm, width 100 cm, height 60 cm. The lysimeters were filled with different soil materials, which were recently used for embankment construction in Germany. With the obtained data, we will develop a time series analysis model to predict total and dissolved metal concentration in road runoff and in soil solution of the roadside embankments. The time series consisted of monthly measurements of heavy metals and was transformed to a stationary situation. Subsequently, the transformed data will be used to conduct analyses in the time domain in order to obtain the parameters of a seasonal autoregressive integrated moving average (ARIMA) model. Four phase approaches for identifying and fitting ARIMA models will be used: identification, parameter estimation, diagnostic checking, and forecasting. An automatic selection criterion, such as the Akaike information criterion, will use to enhance this flexible approach to model building

  19. Electrodeposition of magnesium and magnesium/aluminum alloys

    DOEpatents

    Mayer, A.

    1988-01-21

    Electrolytes and plating solutions for use in processes for electroplating and electroforming pure magnesium and alloys of aluminum and magnesium and also electrodeposition processes. An electrolyte of this invention is comprised of an alkali metal fluoride or a quaternary ammonium halide, dimethyl magnesium and/or diethyl magnesium, and triethyl aluminum and/or triisobutyl aluminum. An electrolyte may be dissolved in an aromatic hydrocarbon solvent to form a plating solution. The proportions of the component compounds in the electrolyte are varied to produce essentially pure magnesium or magnesium/aluminum alloys having varying selected compositions.

  20. Electrodeposition of magnesium and magnesium/aluminum alloys

    DOEpatents

    Mayer, Anton

    1988-01-01

    Electrolytes and plating solutions for use in processes for electroplating and electroforming pure magnesium and alloys of aluminum and magnesium and also electrodeposition processes. An electrolyte of this invention is comprised of an alkali metal fluoride or a quaternary ammonium halide, dimethyl magnesium and/or diethyl magnesium, and triethyl aluminum and/or triisobutyl aluminum. An electrolyte may be dissolved in an aromatic hydrocarbon solvent to form a plating solution. The proportions of the component compounds in the electrolyte are varied to produce essentially pure magnesium or magnesium/aluminum alloys having varying selected compositions.

  1. Mechanical alloying synthesis of K{sub 2}Bi{sub 8}Se{sub 13}-type solid solutions.

    SciTech Connect

    Toumpas, N.; Kyratsi, T.; Hatzikraniotis, E.; Tsiappos, A.; Pavlidou, E.; Paraskevopoulos, K. M.; Chung, D. Y.; Kanatzidis, M. G.; Materials Science Division; Univ. of Cyprus; Aristotle Univ. Thessaloniki; Northwestern Univ.

    2008-01-01

    Solid solutions of K{sub 2}Bi{sub 8-x}Sb{sub x}Se{sub 13} are an interesting series of materials for thermoelectric investigations due to their very low thermal conductivity and highly anisotropic electrical properties. In this work, we aimed to synthesize solid solutions of O-K{sub 2}Bi{sub 8-x}Sb{sub x}Se{sub 13} type materials using powder techniques. The synthesis was based on mechanical alloying as well as sintering procedures. The products were studied in terms of structural features, composition and purity with powder x-ray diffraction, scanning electron microscopy and energy dispersive spectroscopy. Preliminary results on thermoelectric properties as well as IR reflectivity measurements are presented.

  2. Study on Variants of Solution Treatment and Aging Cycle of Titanium Alloy Ti6Al4V

    NASA Astrophysics Data System (ADS)

    Gupta, R. K.; Kumar, V. Anil; Chhangani, Sumit

    2016-04-01

    Ti6Al4V with two different chemical compositions, one rich and the other lean in α-stabilizer oxygen were selected to study the effect of quench severity during solution treatment and their aging response. These two coupons were taken from two differently processed wrought products viz. rolled ring and closed die forging. The coupons were then subjected to solution treatment followed by employing different cooling rates to vary the quench severity and different aging treatments by changing the aging temperature and time. The microstructure and mechanical properties thus obtained are correlated with respect to the heat treatment conditions. It is noted that there is a significant increase in strength of the alloy retaining the ductility when it is aged in the aging temperature regime of 550-650 °C and time of 8 h. Role of higher oxygen content is noted, which is more pronounced with higher severity of quench (by water quenching). Specimens representative of different heat treatment conditions were characterized using optical microscope, electron back-scattered diffraction, and electron microscope. The presence of martensitic (α') structure along with uniform distribution of fine primary α, secondary α precipitates and refined β-grains, twins in the microstructure helps in improving the strength of the material. Also, during high temperature aging of 700 °C, which incidentally falls in the range of annealing temperature of the alloy, overaging occurs which is similar to effect of annealing and hence retains the ductility as well.

  3. Reducing emissions from uranium dissolving

    SciTech Connect

    Griffith, W.L.; Compere, A.L.; Huxtable, W.P.; Googin, J.M.

    1992-10-01

    This study was designed to assess the feasibility of decreasing NO[sub x] emissions from the current uranium alloy scrap tray dissolving facility. In the current process, uranium scrap is dissolved in boiling nitric acid in shallow stainless-steel trays. As scrap dissolves, more metal and more nitric acid are added to the tray by operating personnel. Safe geometry is assured by keeping liquid level at or below 5 cm, the depth of a safe infinite slab. The accountability batch control system provides additional protection against criticality. Both uranium and uranium alloys are dissolved. Nitric acid is recovered from the vapors for reuse. Metal nitrates are sent to uranium recovery. Brown NO[sub x] fumes evolved during dissolving have occasionally resulted in a visible plume from the trays. The fuming is most noticeable during startup and after addition of fresh acid to a tray. Present environmental regulations are expected to require control of brown NO[sub x] emissions. A detailed review of the literature, indicated the feasibility of slightly altering process chemistry to favor the production of NO[sub 2] which can be scrubbed and recycled as nitric acid. Methods for controlling the process to manage offgas product distribution and to minimize chemical reaction hazards were also considered.

  4. Reducing emissions from uranium dissolving

    SciTech Connect

    Griffith, W.L.; Compere, A.L.; Huxtable, W.P.; Googin, J.M.

    1992-10-01

    This study was designed to assess the feasibility of decreasing NO{sub x} emissions from the current uranium alloy scrap tray dissolving facility. In the current process, uranium scrap is dissolved in boiling nitric acid in shallow stainless-steel trays. As scrap dissolves, more metal and more nitric acid are added to the tray by operating personnel. Safe geometry is assured by keeping liquid level at or below 5 cm, the depth of a safe infinite slab. The accountability batch control system provides additional protection against criticality. Both uranium and uranium alloys are dissolved. Nitric acid is recovered from the vapors for reuse. Metal nitrates are sent to uranium recovery. Brown NO{sub x} fumes evolved during dissolving have occasionally resulted in a visible plume from the trays. The fuming is most noticeable during startup and after addition of fresh acid to a tray. Present environmental regulations are expected to require control of brown NO{sub x} emissions. A detailed review of the literature, indicated the feasibility of slightly altering process chemistry to favor the production of NO{sub 2} which can be scrubbed and recycled as nitric acid. Methods for controlling the process to manage offgas product distribution and to minimize chemical reaction hazards were also considered.

  5. Parameterizing the binding properties of dissolved organic matter with default values skews the prediction of copper solution speciation and ecotoxicity in soil.

    PubMed

    Djae, Tanalou; Bravin, Matthieu N; Garnier, Cédric; Doelsch, Emmanuel

    2017-04-01

    Parameterizing speciation models by setting the percentage of dissolved organic matter (DOM) that is reactive (% r-DOM) toward metal cations at a single 65% default value is very common in predictive ecotoxicology. The authors tested this practice by comparing the free copper activity (pCu(2+)  = -log10 [Cu(2+) ]) measured in 55 soil sample solutions with pCu(2+) predicted with the Windermere humic aqueous model (WHAM) parameterized by default. Predictions of Cu toxicity to soil organisms based on measured or predicted pCu(2+) were also compared. Default WHAM parameterization substantially skewed the prediction of measured pCu(2+) by up to 2.7 pCu(2+) units (root mean square residual = 0.75-1.3) and subsequently the prediction of Cu toxicity for microbial functions, invertebrates, and plants by up to 36%, 45%, and 59% (root mean square residuals ≤9 %, 11%, and 17%), respectively. Reparametrizing WHAM by optimizing the 2 DOM binding properties (i.e., % r-DOM and the Cu complexation constant) within a physically realistic value range much improved the prediction of measured pCu(2+) (root mean square residual = 0.14-0.25). Accordingly, this WHAM parameterization successfully predicted Cu toxicity for microbial functions, invertebrates, and plants (root mean square residual ≤3.4%, 4.4%, and 5.8%, respectively). Thus, it is essential to account for the real heterogeneity in DOM binding properties for relatively accurate prediction of Cu speciation in soil solution and Cu toxic effects on soil organisms. Environ Toxicol Chem 2017;36:898-905. © 2016 SETAC. © 2016 SETAC.

  6. Corrosion kinetics and topography analysis of Ti-6Al-4V alloy subjected to different mouthwash solutions.

    PubMed

    Faverani, Leonardo Perez; Barao, Valentim Adelino Ricardo; Pires, Maria Flávia Araújo; Yuan, Judy Chia-Chun; Sukotjo, Cortino; Mathew, Mathew T; Assunção, Wirley Gonçalves

    2014-10-01

    This study evaluated the corrosion kinetics and surface topography of Ti-6Al-4V alloy exposed to mouthwash solutions (0.12% chlorhexidine digluconate, 0.053% cetylpyridinium chloride and 3% hydrogen peroxide) compared to artificial saliva (pH6.5) (control). Twenty Ti-6Al-4V alloy disks were used and divided into 4 groups (n=5). For the electrochemical assay, standard tests as open circuit potential and electrochemical impedance spectroscopy (EIS) were applied at baseline, 7 and 14days after immersion in the solutions. Scanning electron microscopy, atomic force microscopy and profilometry (average roughness - Ra) were used for surface characterization. Total weight loss of disks was calculated. Data were analyzed by ANOVA and Bonferroni's test (α=0.05). Hydrogen peroxide generated the lowest polarization resistance (Rp) values for all periods (P<0.05). For the capacitance (Cdl), similar results were observed among groups at baseline (P=0.098). For the 7 and 14-day periods, hydrogen peroxide promoted the highest Cdl values (P<0.0001). Hydrogen peroxide promoted expressive superficial changes and greater Ra values than the others (P<0.0001). It could be concluded that solutions containing cetylpyridinium chloride and chlorhexidine digluconate might be the mouthwashes of choice during the post-operatory period of dental implants. However, hydrogen peroxide is counter-indicated in these situations. Further studies evaluating the dynamics of these solutions (tribocorrosion) and immersing the disks in daily cycles (two or three times a day) to mimic a clinical situation closest to the application of mouthwashes in the oral cavity are warranted to prove our results. Copyright © 2014 Elsevier B.V. All rights reserved.

  7. Structure and Phase Composition of Ni-Al-Cr Alloy Alloyed by Rhenium and Lanthanum

    NASA Astrophysics Data System (ADS)

    Nikonenko, E. L.; Popova, N. A.; Dement, T. V.; Koneva, N. A.

    2017-06-01

    The paper presents the transmission and the scanning electron microscope investigations of the phase composition and fine structure of Ni-Al-Cr-based alloy alloyed by rhenium and lanthanum. The alloy is prepared by the directional crystallization technique and then subjected to 1150°C annealing during 1 hour. It is shown that γ- and γ'-phases are major and have a face-centered cubic crystal system. Solid solutions of γ- and γ'-phase have a disordered and an ordered atom arrangement, respectively. The latter has L12 superstructure. It is found that rhenium and lanthanum alloying leads to the structural modification of γ'-phase quasi-cuboids. Not dissolving in major phases, rhenium and lanthanum are phase-formation elements and form σ-phase. The phase composition and morphology of these phases are studied and described.

  8. Dependence of Microstructure on Solution and Aging Treatment for Near-β Forged TA15 Ti-Alloy

    NASA Astrophysics Data System (ADS)

    Sun, Zhichao; Wu, Huili; Ma, Xiaoyong; Mao, Xiaojun; Yang, He

    2016-10-01

    For TA15 Ti-alloy, a tri-modal microstructure was obtained via near-β forging combined with solution and aging treatment (SAT) with a short time of air cooling (AC) during forgings transferring before water quenching (WQ). The influence of SAT conditions on final microstructures via 970 °C/0.1 s-1/60%/(AC + WQ) and SAT was investigated. Solution temperature determined the proportion of α and β phases and mainly affected the volume fraction of secondary lamellar α. Solution time mainly influenced the morphology of secondary lamellar α. Solution cooling method was the main factor affecting the thickness of lamellar α. Lower cooling rate resulted in more and thicker lamellar α. Aging treatment had little influence on the volume fraction, size, and morphology of each phase in the microstructure. The main function of aging treatment was to homogenize and stabilize the microstructure. The volume fraction and thickness of lamellar α were increased, and the distribution homogeneity became better during aging. Under the given forging condition, the reasonable solution and aging conditions to obtain tri-modal microstructure were determined as 930 °C/1~2 h/AC + 550~600 °C/5 h/AC.

  9. Effect of Heat Treatment on Electrochemical Properties of Mg-9 wt.%Al-2.5 wt.%Pb Alloy in Sodium Chloride Solution

    NASA Astrophysics Data System (ADS)

    Wang, Linqian; Wang, Richu; Feng, Yan; Deng, Min; Wang, Naiguang

    2017-02-01

    Mg-Al-Pb alloy can serve as a good candidate for the anode material in seawater-activated batteries. The effect of solution and aging treatment on electrochemical properties of Mg-9 wt.%Al-2.5 wt.%Pb alloy in 3.5 wt.% NaCl solution was investigated through scanning electron microscopy and electrochemical tests. The results indicate that the discharge activity of Mg-9 wt.%Al-2.5 wt.%Pb alloy decreases after solution treatment, although its anodic efficiency increases slightly. In contrast, its discharge performance and anodic efficiency, which are crucial for the application of batteries, are both enhanced after aging at 200°C for 12 h.

  10. Effect of Minor Zn Additions on the Mechanical and Corrosion Properties of Solution-Treated AM60-2%RE Magnesium Alloy

    NASA Astrophysics Data System (ADS)

    Liu, Z. L.; Liu, Y.; Liu, X. Q.; Wang, M. M.

    2016-07-01

    The microstructure, mechanical properties, and corrosion behaviors of solution-treated AM60-2%RE magnesium alloy containing 0.2-0.8% wt.% Zn were investigated. With the increase of Zn, the volume fraction of dispersed rod-like Al4RE and granular-like Al11RE3 phases of solution-treated AM60-2%RE + x%Zn increased, which improved the mechanical properties by dispersion strengthening. With increasing Zn content, the corrosion current density decreased, and the corrosion potential and electrochemical impedance of the alloys increased, and the corrosion resistance of solution-treated AM60-2%RE + x%Zn was improved. With the increase of Zn content, the leaf-like corrosion products of the alloy became smaller and more compact, and the content of Zn, Al, Ce, and La in corrosion products increased, which was beneficial to inhibit the corrosion progress.

  11. Characterization of the corrosion resistance of several alloys to dilute biologically active solutions

    NASA Technical Reports Server (NTRS)

    Walsh, Daniel W.

    1990-01-01

    Sulfate reducing bacteria and acid producing bacteria/fungi detected in hygiene waters increased the corrosion rate in aluminum alloy. Biologically active media enhanced the formation of pits on metal coupons. Direct observation of gas evolved at the corrosion sample, coupled with scanning electron microscopy (SEM) and energy dispersive x-ray analysis of the corrosion products indicates that the corrosion rate is increased because the presence of bacteria favor the reduction of hydrogen as the cathodic reaction through the reaction of oxygen and water. SEM verifies the presence of microbes in a biofilm on the surface of corroding samples. The bacterial consortia are associated with anodic sites on the metal surface, aggressive pitting occurs adjacent to biofilms. Many pits are associated with triple points and inclusions in the aluminum alloy microstructure. Similar bacterial colonization was found on the stainless steel samples. Fourier transform Infrared Spectroscopy confirmed the presence of carbonyl groups in pitted areas of samples exposed to biologically active waters.

  12. Microstructure evolution in solution treated Ti15Mo alloy processed by high pressure torsion

    SciTech Connect

    Janeček, Miloš; Čížek, Jakub; Stráský, Josef; Václavová, Kristína; Hruška, Petr; Polyakova, Veronika; Gatina, Svetlana; Semenova, Irina

    2014-12-15

    Microstructure evolution and mechanical properties of ultra-fine grained Ti15Mo alloy processed by high pressure torsion were investigated. High pressure torsion straining resulted in strong grain refinement as-observed by transmission electron microscopy. Microhardness and light microscopy showed two distinct regions — (i) a central region with radial material flow and low microhardness (340 HV) and (ii) a peripheral region with rotational material flow and high microhardness (430 HV). Positron annihilation spectroscopy showed that the only detectable defects in the material are dislocations, whose density increases with the radial distance and the number of high pressure torsion revolutions. The local chemical environment around defects does not differ significantly from the average composition. - Highlights: • Beta-Ti alloy Ti15Mo was processed by high pressure torsion (HPT). • Lateral inhomogeneity of the microstructure and microhardness was found. • Dislocations are the only lattice defects detectable by positron annihilation. • Molybdenum is not preferentially segregated along dislocation cores.

  13. Atomistic Simulations of Dislocations in a Model BCC Multicomponent Concentrated Solid Solution Alloy (Postprint)

    DTIC Science & Technology

    2016-12-19

    COPY) AIR FORCE RESEARCH LABORATORY MATERIALS AND MANUFACTURING DIRECTORATE WRIGHT-PATTERSON AIR FORCE BASE, OH 45433-7750 AIR FORCE MATERIEL...SPONSORING/MONITORING AGENCY ACRONYM(S) Air Force Research Laboratory Materials and Manufacturing Directorate Wright-Patterson Air Force Base, OH...shallower temperature dependence of the strengthening, as compared to pure BCC Fe as well as a reference mean-field BCC alloy material of the same

  14. Transformation of Metastable β-Solid Solution in Alloy VTI-4

    NASA Astrophysics Data System (ADS)

    Demakov, S. L.; Karabanalov, M. S.; Oleneva, O. A.

    2015-01-01

    Phase transformations in aging of alloy VTI-4 quenched from the β-domain are studied in the temperature range of 550 - 750°C. Two morphological types of precipitates of an orthorhombic O-phase are detected. A scheme of evolution of the transformations is suggested. Variation of the lattice constants of the β- and O-phases and of the hardness in the aging process is plotted.

  15. Three dimensional thermal-solute phase field simulation of binary alloy solidification

    NASA Astrophysics Data System (ADS)

    Bollada, P. C.; Goodyer, C. E.; Jimack, P. K.; Mullis, A. M.; Yang, F. W.

    2015-04-01

    We employ adaptive mesh refinement, implicit time stepping, a nonlinear multigrid solver and parallel computation to solve a multi-scale, time dependent, three dimensional, nonlinear set of coupled partial differential equations for three scalar field variables. The mathematical model represents the non-isothermal solidification of a metal alloy into a melt substantially cooled below its freezing point at the microscale. Underlying physical molecular forces are captured at this scale by a specification of the energy field. The time rate of change of the temperature, alloy concentration and an order parameter to govern the state of the material (liquid or solid) are controlled by the diffusion parameters and variational derivatives of the energy functional. The physical problem is important to material scientists for the development of solid metal alloys and, hitherto, this fully coupled thermal problem has not been simulated in three dimensions, due to its computationally demanding nature. By bringing together state of the art numerical techniques this problem is now shown here to be tractable at appropriate resolution with relatively moderate computational resources.

  16. The source of dissolved silicon in soil surface solutions of a temperate forest ecosystem: Ge/Si and Si isotope ratios as biogeochemical tracers

    NASA Astrophysics Data System (ADS)

    Cornelis, J.; Delvaux, B.; Cardinal, D.; André, L.; Ranger, J.; Opfergelt, S.

    2010-12-01

    Understand the biogeochemical cycle of silicon (Si) in the Earth’s critical zone and the dissolved Si transfer from the litho-pedosphere into the hydrosphere is of great interest for the global balance of biogeochemical processes, including the global C cycle. Indeed, the interaction between Si and C cycles regulates the atmospheric CO2 through the chemical weathering of silicate minerals, the C sequestration in stable organo-mineral compounds and the Si nutrition of phytoplankton CO2-consumers in oceans. H4SiO4 released by mineral dissolution contributes to the critical zone evolution through neoformation of secondary minerals, adsorption onto hydroxyl-bearing phases and recycling by vegetation and return of phytoliths on topsoil. The neoformation of secondary precipitates (clay minerals and phytoliths polymerized in plants) and adsorption of Si onto Fe and Al (hydr)oxides are processes favoring the light Si isotope incorporation, generating rivers enriched in heavy Si isotopes. On the other hand, clay minerals and phytoliths display contrasting Ge/Si ratios since clay-sized weathering products are enriched in Ge and phytoliths are depleted in Ge. Thus stable Si isotope and Ge/Si ratios constitute very interesting proxies to trace transfer of Si in the critical zone. Here we report Si isotopic and Ge/Si ratios of the different Si pools in a temperate soil-tree system (Breuil experimental forest, France) involving various tree species grown on Alumnic Cambisol derived from granitic bedrock. Relative to granitic bedrock (δ30Si = -0.07 ‰; Ge/Si = 2.5 µmol/mol), clay-sized minerals are enriched in 28Si (-1.07 ‰) and Ge (6.2 µmol/mol) while phytoliths are enriched in 28Si (-0.28 to -0.64 ‰) and depleted in Ge (0.1 to 0.3 µmol/mol). This contrast allows us to infer the relative contribution of litho/pedogenic and biogenic mineral dissolution on the release of H4SiO4 in soil surface solutions. The Si-isotope signatures and Ge/Si ratios of forest floor

  17. Effect of dissolved oxygen on the photodecomposition of monochloramine and dichloramine in aqueous solution by UV irradiation at 253.7 nm.

    PubMed

    De Laat, Joseph; Boudiaf, Nicolas; Dossier-Berne, Florence

    2010-05-01

    The effect of dissolved oxygen on the photodecomposition of monochloramine (7.5 < pH < 10) and dichloramine (pH = 3.7 +/- 0.2) at 253.7 nm has been investigated. The kinetic study shows that the rate of photodecomposition of monochloramine is about two times faster in the absence of oxygen than in the presence of oxygen, is not significantly affected by pH and by the presence of hydroxyl radical scavengers (hydrogenocarbonate ion and tert-butanol). The apparent quantum yields of photodecomposition of monochloramine at 253.7 nm ([NH(2)Cl](0) approximately 1.5-2 mM, epsilon(253.7 nm) = 371 M(-1) cm(-1)) were equal to 0.28 +/- 0.03 and 0.54 +/- 0.03 mol E(-1) in oxygenated-saturated and in oxygen-free solutions, respectively. The photodecomposition rates or the apparent quantum yields of photodecomposition of dichloramine ([NHCl(2)](0) approximately 1.5-2 mM, pH = 3.7 +/- 0.2) in oxygen-free and in oxygen-saturated solutions were quite identical (Phi = 0.82 +/- 0.08 mol E(-1); epsilon(253.7 nm) = 126 M(-1) cm(-1)). Under O(2) saturation, UV irradiation of NH(2)Cl leads to the formation of nitrite ( approximately 0.37 mol/mol of NH(2)Cl decomposed), nitrate ( approximately 0.073 mol/mol) and does not form ammonia (<0.01 mol/mol). In oxygen-free solutions, monochloramine decomposes to form ammonia ( approximately 0.37 mol/mol). Photodecomposition of dichloramine did not lead to significant amounts of nitrite and nitrate in the presence and in the absence of oxygen. The nitrogen mass balances also indicate the formation of other nitrogen species (probably N(2) and/or N(2)O) during the photodecomposition of monochloramine and dichloramine by UV irradiation at 253.7 nm.

  18. Effect of cleanser solutions on the color of acrylic resins associated with titanium and nickel-chromium alloys.

    PubMed

    Freitas Oliveira Paranhos, Helena de; Bezzon, Osvaldo Luiz; Davi, Letícia Resende; Felipucci, Daniela Nair Borges; Silva, Cláudia Helena Lovato da; Pagnano, Valéria Oliveira

    2014-01-01

    This study evaluated the effect of cleanser solutions on the color of heat-polymerized acrylic resin (HPAR) and on the brightness of dental alloys with 180 immersion trials. Disk-shaped specimens were made with I) commercially pure titanium, II) nickel-chromium-molybdenum-titanium, III) nickel-chromium molybdenum, and IV) nickel-chromium-molybdenum beryllium. Each cast disk was invested in the flasks, incorporating the metal disk into the HPAR. The specimens (n=5) were then immersed in solutions containing: 0.05% sodium hypochlorite, 0.12% chlorhexidine digluconate, 0.500 mg cetylpyridinium chloride, a citric acid tablet, one of two different sodium perborate/enzyme tablets, and water. The color measurements (∆E) of the HPAR were determined by a colorimeter in accordance with the National Bureau of Standards. The surface brightness of the metal was visually examined for the presence of tarnish. The results (ANOVA; Tukey test-α=0.05) show that there was a significant difference between the groups (p<0.001) but not among the solutions (p=0.273). The highest mean was obtained for group III (5.06), followed by group II (2.14). The lowest averages were obtained for groups I (1.33) and IV (1.35). The color changes in groups I, II and IV were slight but noticeable, and the color change was considerable for group III. The visual analysis showed that 0.05% sodium hypochlorite caused metallic brightness changes in groups II and IV. It can be concluded that the agents had the same effect on the color of the resin and that the metallic alloys are not resistant to the action of 0.05% sodium hypochlorite.

  19. Effects of applied potential on the stress corrosion cracking behavior of 7003 aluminum alloy in acid and alkaline chloride solutions

    NASA Astrophysics Data System (ADS)

    Zhang, Xiao-yan; Song, Ren-guo; Sun, Bin; Lu, Hai; Wang, Chao

    2016-07-01

    Potentiodynamic polarization tests and slow strain rate test (SSRT) in combination with fracture morphology observations were conducted to investigate the stress corrosion cracking (SCC) behavior of 7003 aluminum alloy (AA7003) in acid and alkaline chloride solutions under various applied potentials ( E a). The results show that AA7003 is to a certain extent susceptible to SCC via anodic dissolution (AD) at open-circuit potential (OCP) and is highly susceptible to hydrogen embrittlement (HE) at high negative E a in the solutions with pH levels of 4 and 11. The susceptibility increases with negative shift in the potential when E a is less than -1000 mV vs. SCE. However, the susceptibility distinctly decreases because of the inhibition of AD when E a is equal to -1000 mV vs. SCE. In addition, the SCC susceptibility of AA7003 in the acid chloride solution is higher than that in the alkaline solution at each potential. Moreover, the effect of hydrogen on SCC increases with increasing hydrogen ion concentration.

  20. Synergism between cerium nitrate and sodium dodecylbenzenesulfonate on corrosion of AA5052 aluminium alloy in 3 wt.% NaCl solution

    NASA Astrophysics Data System (ADS)

    Liu, Jie; Wang, Dapeng; Gao, Lixin; Zhang, Daquan

    2016-12-01

    The synergistic inhibition effect of rare earth cerium nitrate and sodium dodecylbenzenesulfonate (DBS) on corrosion of AA5052 aluminium alloy in 3 wt.% NaCl solution was investigated by electrochemical impedance spectroscopy (EIS), potentiodynamic polarization curve, scanning electron microscope (SEM) and Fourier transform infrared spectroscopy (FT-IR). The results show that the single cerium nitrate or DBS has a limited inhibition effect against corrosion of AA5052 alloy. The combination cerium ions with DBS produced strong synergistic effect on corrosion inhibition for AA5052 alloy and rendered a negaitve shift of the corrosion potential. The formation of the complex of Al(DBS)3 and Ce(DBS)3 stabilized the passive film of Al2O3 and CeO2, retarding both the cathodic and anodic processes of AA5052 alloy corrosion reaction significantly.

  1. Corrosion Behaviour of Nitrogen-Implantation Ti-Ta-Nb Alloy in Physiological Solutions Simulating Real Conditions from Human Body

    NASA Astrophysics Data System (ADS)

    Drob, Silviu Iulian; Vasilescu, Cora; Drob, Paula; Vasilescu, Ecaterina; Gordin, Doina Margareta; Gloriant, Thierry

    2015-04-01

    We applied a new nitrogen-implantation technique (trademark Hardion+) using a source of nitrogen ions, electron cyclotron resonance that assures higher energy and deeper implantation than the conventional techniques. The N-implantation surface of the new Ti-25Ta-25Nb alloy was analyzed as follows: for the phase identification by x-ray diffraction (XRD) in a glancing geometry (1°); for the hardness by the nano-indentation method; for the corrosion behaviour in Ringer solutions of different pH values (simulating the real conditions from the human body) by cyclic and linear polarization, electrochemical impedance spectroscopy and the monitoring of the open circuit potentials and corresponding potential gradients. XRD pattern was indexed with face-centred cubic TiN compound partially substituted with TaN and NbN. The hardness increased about 2 times for the N-implantation alloy. The implantation layer had a protection effect, increasing the corrosion and passivation potentials and decreasing the tendency to passivation and passive current density, due to its compactness, reinforcement action. The corrosion current density and rate decreased by about 10 times and the polarization resistance increased by about 2 times, indicative of a more resistant nitride layer. The porosity was much reduced and the protection efficiency had values closed to 90%, namely the implantation treatment led to the formation of a dense, resistant layer. Impedance spectra showed that the capacitive behaviour of the N-implantation alloy was more insulating and protective. An electric equivalent circuit with two times constants was modelled.

  2. Electrochemical performances of Al-0.5Mg-0.1Sn-0.02In alloy in different solutions for Al-air battery

    NASA Astrophysics Data System (ADS)

    Jingling, Ma; Jiuba, Wen; Hongxi, Zhu; Quanan, Li

    2015-10-01

    In this research, the corrosion behavior and the electrochemical performances of Al-0.5Mg-0.1Sn-0.02In (wt.%) alloy have been investigated in 2 M NaCl, 4 M NaOH ethanol-10% water, 4 M NaOH solutions. The results show that the optimal electrochemical properties are obtained in 4 M NaOH ethanol-water solutions, and the alloy has higher anodic utilization and lower self-corrosion rate in the solutions compared to 2 M NaCl or 4 M aqueous NaOH. SEM and EIS results of the alloy are in good agreement with corrosion characteristics. By comparison with the electrochemical performance of Zn in 4 M NaOH solutions, the feasibility of using Al-0.5Mg-0.1Sn-0.02In alloy as anode material for a high power density Al-air battery in 4 M NaOH ethanol-water solutions is demonstrated.

  3. Composition design for Laves phase-related body-centered cubic-V solid solution alloys with large hydrogen storage capacities.

    PubMed

    Wang, H B; Wang, Q; Dong, C; Yuan, L; Xu, F; Sun, L X

    2008-03-19

    This paper analyzes the characteristics of alloy compositions with large hydrogen storage capacities in Laves phase-related body-centered cubic (bcc) solid solution alloy systems using the cluster line approach. Since a dense-packed icosahedral cluster A(6)B(7) characterizes the local structure of AB(2) Laves phases, in an A-B-C ternary system, such as Ti-Cr (Mn, Fe)-V, where A-B forms AB(2) Laves phases while A-C and B-C tend to form solid solutions, a cluster line A(6)B(7)-C is constructed by linking A(6)B(7) to C. The alloy compositions with large hydrogen storage capacities are generally located near this line and are approximately expressed with the cluster-plus-glue-atom model. The cluster line alloys (Ti(6)Cr(7))(100-x)V(x) (x = 2.5-70 at.%) exhibit different structures and hence different hydrogen storage capacities with increasing V content. The alloys (Ti(6)Cr(7))(95)V(5) and Ti(30)Cr(40)V(30) with bcc solid solution structure satisfy the cluster-plus-glue-atom model.

  4. Hardening behavior after high-temperature solution treatment of Ag-20Pd-12Au-xCu alloys with different Cu contents for dental prosthetic restorations.

    PubMed

    Kim, Yonghwan; Niinomi, Mitsuo; Hieda, Junko; Nakai, Masaaki; Cho, Ken; Fukui, Hisao

    2014-07-01

    Ag-Pd-Au-Cu alloys have been used widely for dental prosthetic applications. Significant enhancement of the mechanical properties of the Ag-20Pd-12Au-14.5Cu alloy as a result of the precipitation of the β' phase through high-temperature solution treatment (ST), which is different from conventional aging treatment in these alloys, has been reported. The relationship between the unique hardening behavior and precipitation of the β' phase in Ag-20Pd-12Au-xCu alloys (x=6.5, 13, 14.5, 17, and 20mass%) subjected to the high-temperature ST at 1123K for 3.6ks was investigated in this study. Unique hardening behavior after the high-temperature ST also occurs in Ag-20Pd-12Au-xCu alloys (x=13, 17, and 20) with precipitation of the β' phase. However, hardening is not observed and the β' phase does not precipitate in the Ag-20Pd-12Au-6.5Cu alloy after the same ST. The tensile strength and 0.2% proof stress also increase in Ag-20Pd-12Au-xCu alloys (x=13, 14.5, 17, and 20) after the high-temperature ST. In addition, these values after the high-temperature ST increase with increasing Cu content in Ag-20Pd-12Au-xCu alloys (x=14.5, 17, and 20). The formation process of the β' phase can be explained in terms of diffusion of Ag and Cu atoms and precipitation of the β' phase. Clarification of the relationship between hardening and precipitation of the β' phase via high-temperature ST is expected to help the development of more effective heat treatments for hardening in Ag-20Pd-12Au-xCu alloys. Copyright © 2014 Elsevier Ltd. All rights reserved.

  5. Electrochemical Investigations of Polycaprolactone-Coated AZ31 Mg Alloy in Earle's Balance Salt Solution and Conventional Simulated Body Fluid

    NASA Astrophysics Data System (ADS)

    Wilke, Benjamin M.; Zhang, Lei

    2016-06-01

    Polycaprolactone (PCL) coating has been shown to increase the corrosion resistance of magnesium alloys when exposed to a simulated body fluid. A PCL dip coating was applied to AZ31 Mg alloy. Samples were immersed in both Earle's Balance Salt Solution (EBSS) and conventional simulated body fluids (c-SBF) up to 14 days. Microscopic morphology, electrochemical impedance spectroscopy, and potentiodynamic polarization tests were performed to evaluate the corrosion behavior changes of PCL coatings against immersion times in EBSS and c-SBF as compared to the uncoated AZ31 substrate. PCL-coated samples demonstrated improved corrosion resistance compared to bare AZ31 in both EBSS and c-SBF, indicating that the PCL coating exhibited good corrosion protection of AZ31 in simulated body fluid. Samples immersed in EBSS showed significantly higher electrochemical impedance values and slower corrosion progression as compared to the samples in c-SBF, because of the decreased chloride content and CO2 buffering mechanism of the EBSS.

  6. Electrochemical corrosion and modeling studies of types 7075 and 2219 aluminum alloys in a nitric acid + ferric sulfate deoxidizer solution

    NASA Astrophysics Data System (ADS)

    Savas, Terence P.

    The corrosion behavior of types 7075-T73 and 2219-T852 high strength aluminum alloys have been investigated in a HNO3 + Fe2(SO 4)3 solution. The materials are characterized in the time domain using the electrochemical noise resistance parameter (Rn) and in the frequency-domain using the spectral noise impedance parameter ( Rsn). The Rsn parameter is derived from an equivalent electrical circuit model that represents the corrosion test cell schematic used in the present study. These calculated parameters are correlated to each other, and to corresponding scanning electron microscopy (SEM) examinations of the corroded surfaces. In addition, energy dispersive spectroscopy (EDS) spectra are used in conjunction with SEM exams for particle mapping and identification. These constituent particles are characterized with respect to their size and composition and their effect on the localized corrosion mechanisms taking place. Pitting mechanisms are identified as 'circumferential' where the particles appeared noble with respect to the aluminum matrix and by 'selective dissolution' where they are anodic to the aluminum matrix. The electrochemical data are found to be in good agreement with the surface examinations. Specifically, the electrochemical parameters Rn and Rsn were consistent in predicting the corrosion resistance of 7075-T73 to be lower than for the 2219-T852 alloy. Other characteristic features used in understanding the corrosion mechanisms include the open circuit potential (OCP) and coupling-current time records.

  7. Effect of micro-particles on cavitation erosion of Ti6Al4V alloy in sulfuric acid solution.

    PubMed

    Li, D G; Long, Y; Liang, P; Chen, D R

    2017-05-01

    The influences of micro-particles on ultrasonic cavitation erosion of Ti6Al4V alloy in 0.1M H2SO4 solution were investigated using mass loss weight, scanning electron microscopy (SEM) and white light interferometer. Mass loss results revealed that the cavitation erosion damage obviously decreased with increasing particle size and mass concentration. Open circuit potential recorded during cavitation erosion shifted to positive direction with the decreased mass loss. Meanwhile, the mass loss sharply decreased with applying a positive potential during the entire ultrasonic cavitation erosion, and the relationship between the open circuit potential and the cavitation erosion resistance was discussed. Copyright © 2016 Elsevier B.V. All rights reserved.

  8. Bioactive surface modification of Ti-29Nb-13Ta-4.6Zr alloy through alkali solution treatments.

    PubMed

    Takematsu, E; Katsumata, K; Okada, K; Niinomi, M; Matsushita, N

    2016-05-01

    Bioactive surface modification of Ti-29Nb-13Ta-4.6Zr alloy (TNTZ) was performed through three different alkali solution treatments, including the electrochemical (E), hydrothermal (H), and hydrothermal-electrochemical (HE) processes; all of the processes lead to the formation of sodium-contained amorphous titanium oxide layers on TNTZ samples. The TNTZ samples subjected to the E, H, and HE processes exhibit a flat surface, smooth and fine mesh-like structure surface, and rough mesh-like structure surface, respectively. In the bioactive test, namely, simulated body fluid test, apatite inductivity increases as the surface morphology becomes rough. The order of inductivity for the three processes was HE>H>E. The surface chemical composition also affects the apatite induction ability. The surface with fewer niobium species exhibits better apatite inductivity. Copyright © 2016 Elsevier B.V. All rights reserved.

  9. The effect of injected interstitials on void formation in self-ion irradiated nickel containing concentrated solid solution alloys

    NASA Astrophysics Data System (ADS)

    Yang, Tai-ni; Lu, Chenyang; Jin, Ke; Crespillo, Miguel L.; Zhang, Yanwen; Bei, Hongbin; Wang, Lumin

    2017-05-01

    Pure nickel and three nickel containing single-phase concentrated solid solution alloys (SP-CSAs) have been irradiated using 3 MeV Ni2+ ions at 500 °C to fluences of 1.5 ×1016 and 5.0 ×1016 cm-2 . The radiation-induced voids were characterized using cross sectional transmission electron microscopy that distributions of voids and dislocation loops were presented as a function of depth. A various degree of void suppression was observed on the tested samples and a defect clusters migration mechanism was proposed for NiCo. In order to sufficiently understand the defect dynamics in these SP-CSAs, the injected interstitial effect has been taken into account along with the 1-dimentional (1-D) and 3-dimentional (3-D) interstitial movement mechanisms.

  10. The effect of injected interstitials on void formation in self-ion irradiated nickel containing concentrated solid solution alloys

    DOE PAGES

    Yang, Tai-ni; Lu, Chenyang; Jin, Ke; ...

    2017-02-21

    Pure nickel and three nickel containing single-phase concentrated solid solution alloys (SP-CSAs) have been irradiated using 3 MeV Ni2+ ions at 500 C to fluences of 1.5 x 1016 and 5.0 x 1016 cm2. We characterized the radiation-induced voids using cross sectional transmission electron microscopy that distributions of voids and dislocation loops were presented as a function of depth. We also observed a various degree of void suppression on the tested samples and a defect clusters migration mechanism was proposed for NiCo. Furthermore, in order to sufficiently understand the defect dynamics in these SP-CSAs, the injected interstitial effect has beenmore » taken into account along with the 1-dimentional (1-D) and 3-dimentional (3-D) interstitial movement mechanisms.« less

  11. Structure and Mechanical Properties of Magnesium-Titanium Solid Solution Thin Film Alloys Prepared by Magnetron-sputter Deposition

    NASA Astrophysics Data System (ADS)

    Haddad, Daad; Song, GuangLing; Cheng, Yang Tse

    Mg alloys are being considered for wider application in automotive industry. Designing new alloys with improved mechanical properties is important to the development of new Mg alloy parts. Mg-Ti is an interesting alloying system that may have good corrosion resistance due to high passivity of Ti. However it is difficult to form through a conventional metallurgical method due to the mutual insolubility of Mg and Ti and the big difference in their melting point. Nevertheless, if the alloy can be formed, it may have other unexpected physical and chemical performance. Therefore, it is of significance to understand the properties of Mg-Ti alloy produced by non-conventional approach.

  12. Structural analysis and magnetic properties of solid solutions of Co-Cr system obtained by mechanical alloying

    NASA Astrophysics Data System (ADS)

    Betancourt-Cantera, J. A.; Sánchez-De Jesús, F.; Bolarín-Miró, A. M.; Betancourt, I.; Torres-Villaseñor, G.

    2014-03-01

    In this paper, a systematic study on the structural and magnetic properties of Co100-xCrx alloys (0alloying is presented. Co and Cr elemental powders were used as precursors, and mixed in an adequate weight ratio to obtain Co1-xCrx (0solutions based on Co-hcp, Co-fcc and Cr-bcc structures were obtained. The saturation polarization indicated a maximum value of 1.17 T (144 Am2/kg) for the Co90Cr10, which decreases with the increasing of the Cr content up to x=80, as a consequence of the dilution effect of the magnetic moment which is caused by the Cr content and by the competition between ferromagnetic and antiferromagnetic exchange interactions. The coercivity increases up to 34 kA/m (435 Oe) for Co40Cr60. For Cr rich compositions, it is observed an important decrease reaching 21 kA/m (272 Oe) for Co10Cr90, it is related to the grain size and the structural change. Besides, the magnetic anisotropy constant was determined for each composition. Magnetic thermogravimetric analysis allowed to obtain Curie temperatures corresponding to the formation of hcp-Co(Cr) and fcc-Co(Cr) solid solutions.

  13. Extremely high-rate, uniform dissolution of alloy C-22 in anhydrous organic solutions at room temperature

    DOE PAGES

    Schindelholz, Eric J.; Christie, Michael A.; Allwein, Shawn P.; ...

    2016-06-21

    During routine pharmaceutical development and scale-up work, severe corrosion of a Hastelloy Alloy C-22 filter dryer was observed after single, short (several hours) contact with the product slurry at room temperature. Initial investigations showed that the presence of both 2,3-dichloro-5,6-dicyano-1,4-benzoquinone (DDQ) and HCl was sufficient in an acetonitrile solution to cause rapid corrosion of C-22. More detailed mass loss studies showed initial corrosion rates exceeding25 mm/year that then decreased over several hours to steady state rates of 3-5 mm/year. The corrosion was highly uniform. Electrochemical measurements demonstrated that although C-22 is spontaneously passive in acetonitrile solution, the presence of HClmore » leads to the development of a transpassive region. Furthermore, DDQ is a sufficiently strong oxidizer, particularly in acidic solutions, to polarize the C-22 well into the transpassive region, leading to the observed high corrosion rates.« less

  14. In vitro degradation behavior of Fe-20 Mn-1.2C alloy in three different pseudo-physiological solutions.

    PubMed

    Mouzou, Essowè; Paternoster, Carlo; Tolouei, Ranna; Purnama, Agung; Chevallier, Pascale; Dubé, Dominique; Prima, Frédéric; Mantovani, Diego

    2016-04-01

    High manganese austenitic steels such as Fe-20Mn-1.2C alloys are among the most promising candidates for biodegradable stents applications due to their high strength, high ductility and their chemical composition. In the current work, 14 day static in-vitro tests were performed in controlled atmosphere to assess the degradation behavior in three common pseudo-physiological solutions, i.e. commercial Hanks' (CH), modified Hanks' (MH) and albumin-enriched Dulbecco's modified phosphate buffered saline (DPBS) solutions. The degraded samples surfaces as well as the degradation products were characterized by X-ray diffraction (XRD), scanning electron microscopy (SEM) and Fourier transform infrared spectroscopy (FTIR). Degradation of material and degradation products are shown to be strongly dependent on the test medium due to the presence of different ionic species such as HCO3(-), CO3(2-), Cl(-), Ca(2+) or phosphate groups. In both MH and CH solutions, the increased content of HCO3(-) ions seems to promote MnCO3 crystal growth on sample surfaces whereas the presence of albumin and high content of phosphate ions promotes the formation of an amorphous layer rich in phosphates, iron and manganese.

  15. Reducing Emissions from Uranium Dissolving

    SciTech Connect

    Griffith, W.L.

    1992-01-01

    This study was designed to assess the feasibility of decreasing NO{sub x} emissions from the current uranium alloy scrap tray dissolving facility. In the current process, uranium scrap is dissolved in boiling nitric acid in shallow stainless-steel trays. As scrap dissolves, more metal and more nitric acid are added to the tray by operating personnel. Safe geometry is assured by keeping liquid level at or below 5 cm, the depth of a safe infinite slab. The accountability batch control system provides additional protection against criticality. The trays are steam coil heated. The process has operated satisfactorily, with few difficulties, for decades. Both uranium and uranium alloys are dissolved. Nitric acid is recovered from the vapors for reuse. Metal nitrates are sent to uranium recovery. Brown NO{sub x} fumes evolved during dissolving have occasionally resulted in a visible plume from the trays. The fuming is most noticeable during startup and after addition of fresh acid to a tray. Present environmental regulations are expected to require control of brown NO{sub x} emissions. Because NO{sub x} is hazardous, fumes should be suppressed whenever the electric blower system is inoperable. Because the tray dissolving process has worked well for decades, as much of the current capital equipment and operating procedures as possible were preserved. A detailed review of the literature, indicated the feasibility of slightly altering process chemistry to favor the production of NO{sub 2}, which can be scrubbed and recycled as nitric acid. Methods for controlling the process to manage offgas product distribution and to minimize chemical reaction hazards were also considered.

  16. FABRICATION AND PLASTIC BEHAVIOR OF SINGLE CRYSTAL MgO-NiO AND MgO-MnO SOLID SOLUTION ALLOYS,

    DTIC Science & Technology

    A method of producing solid solution MgO-NiO and MgO-MnO single-crystals is presented. The com presive yield strength of MgO is shown to in crease...nearly four-fold when small amounts of either NiO or MnO is in solid solution in MgO. The cleavage and slip behavior of these alloy crystals are found to be identical to that of MgO. (Author)

  17. Corrosion behaviour of magnesium alloys coated with TiN by cathodic arc deposition in NaCl and Na{sub 2}SO{sub 4} solutions

    SciTech Connect

    Altun, Hikmet Sinici, Hakan

    2008-03-15

    Magnesium-based light-metal alloys belong to a class of structural materials with increasing industrial attention. Magnesium alloys show the lowest density among the engineering metallic materials, low cost and large availability. However, the limitations according to mechanical strength and the low corrosion resistance restrict their practical application. In this study, TiN was coated on magnesium-based AZ91 magnesium-aluminium-zinc alloy using cathodic arc PVD process. The corrosion behaviours of uncoated and coated magnesium alloys in 1% NaCl, 3% NaCl and 3% Na{sub 2}SO{sub 4} solutions and the influence of the coatings on the corrosion behaviour of the substrate were investigated utilizing potentiodynamic polarization tests. A potentiostat for electrochemical corrosion tests, a cathodic arc physical vapour deposition coating system for coating processes, a scanning electron microscopy for surface examination and elemental analysis of the coatings were used in this study. It was determined that corrosion resistance of magnesium alloys can be increased with TiN coating on the alloys using cathodic arc PVD process.

  18. Corrosion behavior of as-cast Mg-8Li-3Al+ xCe alloy in 3.5wt% NaCl solution

    NASA Astrophysics Data System (ADS)

    Manivannan, S.; Dinesh, P.; Mahemaa, R.; MariyaPillai, Nandhakumaran; Kumaresh Babu, S. P.; Sundarrajan, Srinivasan

    2016-10-01

    Mg-8Li-3Al+ xCe alloys ( x = 0.5wt%, 1.0wt%, and 1.5wt%) were prepared through a casting route in an electric resistance furnace under a controlled atmosphere. The cast alloys were characterized by X-ray diffraction, optical microscopy, scanning electron microscopy, and energy-dispersive X-ray spectroscopy. The corrosion behavior of the as-cast Mg-8Li-3Al+ xCe alloys were studied under salt spray tests in 3.5wt% NaCl solution at 35°C, in accordance with standard ASTM B-117, in conjunction with potentiodynamic polarization (PDP) tests. The results show that the addition of Ce to Mg-8Li-3Al (LA83) alloy results in the formation of Al2Ce intermetallic phase, refines both the α-Mg phase and the Mg17Al12 intermetallic phase, and then increases the microhardness of the alloys. The results of PDP and salt spray tests reveal that an increase in Ce content to 1.5wt% decreases the corrosion rate. The best corrosion resistance is observed for the LA83 alloy sample with 1.0wt% Ce.

  19. Corrosion Behavior of Additive Manufactured Ti-6Al-4V Alloy in NaCl Solution

    NASA Astrophysics Data System (ADS)

    Yang, Jingjing; Yang, Huihui; Yu, Hanchen; Wang, Zemin; Zeng, Xiaoyan

    2017-07-01

    The microstructures, potentiodynamic curves, and electrochemical impedance spectroscopy are characterized for Ti-6Al-4V samples produced by selective laser melting (SLM), SLM followed by heat treatment (HT), wire and arc additive manufacturing (WAAM), and traditional rolling to investigate their corrosion behaviors. Results show that the processing technology acts a significant role in controlling the microstructures, which in turn directly determine their corrosion resistance. The order of corrosion resistance of these samples is SLM < WAAM < rolling < SLM+HT. Among these microstructural factors for influencing corrosion resistance, type of constituent phase is the main one, followed by grain size, and the last is morphology. Finally, the application potentials of additive manufactured Ti-6Al-4V alloy are verified in the aspect of corrosion resistance.

  20. Evolution of ion emission yield of alloys with the nature of the solute. 2: Interpretation

    NASA Technical Reports Server (NTRS)

    Blaise, G.; Slodzian, G.

    1977-01-01

    Solid solutions of transition elements in copper, nickel, cobalt, iron, and aluminum matrices were analyzed by observing secondary ion emissions under bombardment with 6.2-keV argon ions. Enchancement of the production of solute-element ions was observed. An ion emission model is proposed according to which the ion yield is governed by the probability of an atom leaving the metal in a preionized state. The energy distribution of the valence electrons of the solute atoms is the bases of the probability calculation.

  1. Influence of fine-grain and solid-solution strengthening on mechanical properties and in vitro degradation of WE43 alloy.

    PubMed

    Liu, Dexue; Ding, Yutian; Guo, Tingbiao; Qin, Xiaoqiong; Guo, Chenggong; Yu, Shankun; Lin, Shengling

    2014-02-01

    As one of the most important potential candidate alloys for vascular stent application, Mg-Y-Zr based Mg-4.2wt%Y-2.4wt%Nd-0.6wt%Ce(La)-0.5wt%Zr (WE43) alloys were investigated in combination with the forming processes of micro-tubes with 2.0 mm diameter and 0.1 mm wall thickness. Orthogonal experimental design for alloy composition, vacuum melting ingot, heat treatment, integrated plastic deformation and micro-tube forward extrusion are included in the processing procedures. Significant improvements in both the mechanical properties and corrosion resistance in phosphate buffered saline solution for WE43 alloys were achieved through this processing sequence. The influence of the heat treatment and hot extrusion on in vitro degradation and plasticity was found to be associated with grain size reduction and the redistribution of intermetallic particles within the microstructure. As a result, the mechanical properties and the corrosion resistance of Mg alloys can be improved through fine-grain strengthening and solid-solution strengthening to some extent.

  2. Influences of temperature, H2SO4 concentration and Sn content on corrosion behaviors of PbSn alloy in sulfuric acid solution

    NASA Astrophysics Data System (ADS)

    Li, D. G.; Chen, D. R.; Wang, J. D.; Chen, H. S.

    2011-10-01

    The influences of temperature, H2SO4 concentration and Sn content on corrosion behaviors of PbSn alloys in sulfuric acid solution were investigated by potentiodynamic curve, cyclic voltammetry (CV), linear sweeping voltage (LSV), electrochemical impedance spectra (EIS), a.c. voltammetry (ACV) and Mott-Schottky analysis. The microstructure of the corrosion layer on PbSn alloy was analyzed by scanning electron microscopy (SEM). The results showed that the corrosion resistance of PbSn alloy increased with ascending Sn content and H2SO4 concentration, the increment of temperature can decrease the corrosion resistance of PbSn alloy in H2SO4 solution. The conductivity of the anodic film on PbSn alloy was enhanced with increasing temperature, ascending Sn content and descending H2SO4 concentration. SEM result revealed that the corrosion film after cyclic voltammetry was consisted of tetragonal crystal, the porosity enlarged with decreasing temperature, Sn content and H2SO4 concentration.

  3. The Influences of Climate, Landcover, and In-lake Processes on Nitrogen Solutes and Dissolved Organic Carbon in Small Lake-Watersheds on the Southwestern Adirondack Region of New York

    NASA Astrophysics Data System (ADS)

    Ito, M.; Mitchell, M. J.; Driscoll, C. T.; Kretser, W.; Roy, K. M.

    2001-05-01

    In the Adirondack region of New York where soils and surface waters have been found to be highly sensitive to acidic deposition, precipitation concentrations of nitrate have not declined. In order to understand the responses of lake-watersheds to nitrogen deposition in the Adirondack region and to identify effective approaches to deal with potential problems associated with high N deposition, the factors regulating nitrogen solutes in discharge from lake-watersheds are being evaluated. In the present analysis, nitrogen solutes and dissolved organic carbon in two small lake-watersheds were examined from 1999 to 2000 to assess the influences of climate, land cover, and in-lake processes on these solutes in the southwestern part of the Adirondack region where wet deposition of nitrate and nitrate concentrations in surface waters were higher than in other parts of the Adirondacks. The interrelationships among nitrate, ammonium, dissolved organic nitrogen, and dissolved organic carbon were evaluated to assist in characterizing the influences of the above factors.

  4. Corrosion Behavior of HVOF-Sprayed Fe-Based Alloy Coating in Various Solutions

    NASA Astrophysics Data System (ADS)

    Qiao, Lei; Wu, Yuping; Hong, Sheng; Qin, Yujiao; Shi, Wei; Li, Gaiye

    2017-08-01

    A Fe-based amorphous/nanocrystalline coating was prepared by the high-velocity oxygen fuel (HVOF) spraying process. The coating was characterized by x-ray diffraction, scanning electron microscopy and transmission electron microscopy. The corrosion resistances of the Fe-based coating and a reference electroplated hard chromium (EHC) coating were evaluated in a 3.5% NaCl solution, a 1 mol/L HCl solution and a 1 mol/L NaOH solution using potentiodynamic polarization and electrochemical impedance spectroscopy (EIS). All of the results indicated that the corrosion resistance of the Fe-based coating was superior to the resistance of the EHC coating in both the 3.5% NaCl solution and the 1 mol/L HCl solution due to the dense structure and fewer defects of the Fe-based coating. However, the corrosion resistance of the Fe-based coating was inferior to corrosion resistance of the EHC coating in the 1 mol/L NaOH solution. This could be ascribed to the drastic passivation of the EHC coating in an alkaline environment.

  5. In-situ quantification of the effect of solute on the mobility, character and driving pressure of grain boundaries during recrystallization in aluminum alloys

    NASA Astrophysics Data System (ADS)

    Taheri, Mitra L.

    Aluminum alloys exhibit recrystallization kinetics that vary strongly with composition. The conventional understanding is that certain alloying elements, e.g. chromium, retard grain boundary motion due to the formation of tine dispersions of second phase particles, giving rise to particle drag of boundaries. There is countervailing evidence, however, that suggests that solute drag provides the stronger influence on the mobility of grain boundaries. This thesis presents new evidence of this pronounced effect of solute drag based on in-situ annealing (both SEM and TEM) and EBSD experiments involving recrystallization in aluminum alloys with varying composition in which individual boundaries move under the driving pressure of stored energy from prior plastic strain. This driving pressure is calculated both macroscopically (via Calorimetry, Microhardness) and microscopically (via Orientation Imaging Microscopy, Transmission Electron Microscopy). In all alloy compositions studied, a compensation effect is noted with respect to grain boundary mobility maxima for certain boundary types. A shift occurs in the misorientation associated with maximum mobility at 38--39°<111> observed at low temperatures, to misorientation axes towards <001>, <110> and <111> is seen in alloys when annealed at higher temperatures. A faceting/defaceting transition is also observed which is consistent with the changes in maximum mobility boundary type with increased temperature. These observations are supported by analysis of activation energy for boundary migration for each alloy. Evidence for irregular motion of boundaries from in-situ observations is discussed in reference to new theoretical results that suggest that boundaries migrating in the presence of solutes should move sporadically, provided that the length scale at which observations are made is small enough. Z-Contrast Imaging using a Scanning Transmission Electron Microscope coupled with TEM EDX analysis suggested variable Zr

  6. Effect of solution treatment on stress corrosion cracking behavior of an as-forged Mg-Zn-Y-Zr alloy

    PubMed Central

    Wang, S. D.; Xu, D. K.; Wang, B. J.; Sheng, L. Y.; Han, E. H.; Dong, C.

    2016-01-01

    Effect of solid solution treatment (T4) on stress corrosion cracking (SCC) behavior of an as-forged Mg-6.7%Zn-1.3%Y-0.6%Zr (in wt.%) alloy has been investigated using slow strain rate tensile (SSRT) testing in 3.5 wt.% NaCl solution. The results demonstrated that the SCC susceptibility index (ISCC) of as-forged samples was 0.95 and its elongation-to-failure (εf) was only 1.1%. After T4 treatment, the SCC resistance was remarkably improved. The ISCC and εf values of T4 samples were 0.86 and 3.4%, respectively. Fractography and surface observation indicated that the stress corrosion cracking mode for as-forged samples was dominated by transgranular and partially intergranular morphology, whereas the cracking mode for T4 samples was transgranular. In both cases, the main cracking mechanism was associated with hydrogen embrittlement (HE). Through alleviating the corrosion attack of Mg matrix, the influence of HE on the SCC resistance of T4 samples can be greatly suppressed. PMID:27387817

  7. Effect of solution treatment on stress corrosion cracking behavior of an as-forged Mg-Zn-Y-Zr alloy.

    PubMed

    Wang, S D; Xu, D K; Wang, B J; Sheng, L Y; Han, E H; Dong, C

    2016-07-08

    Effect of solid solution treatment (T4) on stress corrosion cracking (SCC) behavior of an as-forged Mg-6.7%Zn-1.3%Y-0.6%Zr (in wt.%) alloy has been investigated using slow strain rate tensile (SSRT) testing in 3.5 wt.% NaCl solution. The results demonstrated that the SCC susceptibility index (ISCC) of as-forged samples was 0.95 and its elongation-to-failure (εf) was only 1.1%. After T4 treatment, the SCC resistance was remarkably improved. The ISCC and εf values of T4 samples were 0.86 and 3.4%, respectively. Fractography and surface observation indicated that the stress corrosion cracking mode for as-forged samples was dominated by transgranular and partially intergranular morphology, whereas the cracking mode for T4 samples was transgranular. In both cases, the main cracking mechanism was associated with hydrogen embrittlement (HE). Through alleviating the corrosion attack of Mg matrix, the influence of HE on the SCC resistance of T4 samples can be greatly suppressed.

  8. Effect of solution treatment on stress corrosion cracking behavior of an as-forged Mg-Zn-Y-Zr alloy

    NASA Astrophysics Data System (ADS)

    Wang, S. D.; Xu, D. K.; Wang, B. J.; Sheng, L. Y.; Han, E. H.; Dong, C.

    2016-07-01

    Effect of solid solution treatment (T4) on stress corrosion cracking (SCC) behavior of an as-forged Mg-6.7%Zn-1.3%Y-0.6%Zr (in wt.%) alloy has been investigated using slow strain rate tensile (SSRT) testing in 3.5 wt.% NaCl solution. The results demonstrated that the SCC susceptibility index (ISCC) of as-forged samples was 0.95 and its elongation-to-failure (εf) was only 1.1%. After T4 treatment, the SCC resistance was remarkably improved. The ISCC and εf values of T4 samples were 0.86 and 3.4%, respectively. Fractography and surface observation indicated that the stress corrosion cracking mode for as-forged samples was dominated by transgranular and partially intergranular morphology, whereas the cracking mode for T4 samples was transgranular. In both cases, the main cracking mechanism was associated with hydrogen embrittlement (HE). Through alleviating the corrosion attack of Mg matrix, the influence of HE on the SCC resistance of T4 samples can be greatly suppressed.

  9. The effect of Pt and Pd alloying additions on the corrosion behavior of titanium in fluoride-containing environments.

    PubMed

    Nakagawa, M; Matono, Y; Matsuya, S; Udoh, K; Ishikawa, K

    2005-05-01

    In this study, we examined the corrosion behaviors of pure titanium, the alloys Ti-6Al-4V and Ti-6Al-7Nb, and the new experimental alloys Ti-Pt and Ti-Pd using anodic polarization and corrosion potential measurements in an environment containing fluoride. Before and after immersion in the test solutions, we made observations using a scanning electron microscope. The test solutions included an artificial saliva containing 0.2% NaF (corresponding to 905 ppm F) and an artificial saliva with a low concentration of oxygen. Although the surfaces of the Ti-Pt and Ti-Pd alloys were not affected by an acidic environment containing fluoride, the surfaces of the pure titanium, the Ti-6Al-4V alloy, and the Ti-6Al-7Nb alloy were markedly roughened by corrosion. The surfaces of the pure titanium, the Ti-6Al-4V alloy, and the Ti-6Al-7Nb alloy were microscopically damaged by corrosion when they were immersed in the solution containing a low concentration of dissolved oxygen, even with a fluoride concentration included in the commercial dentifrices. In this situation, however, the surfaces of the new Ti-Pt and Ti-Pd alloys were not affected. These alloys are expected to be of use in dental work as new titanium alloys with high corrosion resistances.

  10. Alloy softening in binary molybdenum alloys

    NASA Technical Reports Server (NTRS)

    Stephens, J. R.; Witzke, W. R.

    1972-01-01

    An investigation was conducted to determine the effects of alloy additions of Hf, Ta, W, Re, Os, Ir, and Pt on the hardness of Mo. Special emphasis was placed on alloy softening in these binary Mo alloys. Results showed that alloy softening was produced by those elements having an excess of s+d electrons compared to Mo, while those elements having an equal number or fewer s+d electrons than Mo failed to produce alloy softening. Alloy softening and hardening can be correlated with the difference in number of s+d electrons of the solute element and Mo.

  11. A procedure to create isoconcentration surfaces in low-chemical-partitioning, high-solute alloys.

    PubMed

    Hornbuckle, B C; Kapoor, M; Thompson, G B

    2015-12-01

    A proximity histogram or proxigram is the prevailing technique of calculating 3D composition profiles of a second phase in atom probe tomography. The second phase in the reconstruction is delineated by creating an isoconcentration surface, i.e. the precipitate-matrix interface. The 3D composition profile is then calculated with respect to this user-defined isoconcentration surface. Hence, the selection of the correct isoconcentration surface is critical. In general, the preliminary selection of an isoconcentration value is guided by the visual observation of a chemically partitioned second phase. However, in low-chemical -partitioning systems, such a visual guide is absent. The lack of a priori composition information of the precipitate phase may further confound the issue. This paper presents a methodology of selecting an appropriate elemental species and subsequently obtaining an isoconcentration value to create an accurate isoconcentration surface that will act as the precipitate-matrix interface. We use the H-phase precipitate in the Ni-Ti-Hf shape memory alloy as our case study to illustrate the procedure.

  12. Integrated environmental degradation model for Fe-Ni-Cr alloys in irradiated aqueous solutions

    SciTech Connect

    Pleune, T.T.

    1999-09-01

    Environmentally assisted cracking (EAC) is the most problematic form of localized corrosion in irradiated areas of nuclear power plants. EAC is any phenomenon where a combination of environment, material, and tensile stress result in cracking, including stress corrosion cracking (SCC), and hydrogen embrittlement. For this project an integrated EAC model based on first-principles electrochemistry and physical metallurgy was developed. The effect of neutron and gamma radiation dose is included explicitly so that irradiation-assisted SCC can be studied. The primary dependent variable in the model is the environmentally assisted crack growth rate as a function of chemical and mechanical parameters. The model integrates bulk and local chemistry models with the mechanical and chemical (alloy) behavior of the metal to allow the study of EAC in general. The model evaluates the water chemistry including radiolysis and hydrogen water chemistry and metal properties including radiation-induced segregation, radiation hardening, and the crack tip strain rate of a growing crack. The model inputs include thermal-hydraulic data such as flow rate, temperature, power level, dose, pressure, and initial water chemistry throughout the reactor, as well as dimension, stress/strain conditions, and initial sensitization data for reactor components.

  13. Doping and Alloying in the Solution-Phase Synthesis of Germanium Nanocrystals

    SciTech Connect

    Ruddy, D. A.; Neale, N. R.

    2012-01-01

    Group IV nanocrystals (NCs) are receiving increased attention as a potentially non-toxic nanomaterial for use in a number of important optoelectronic applications (e.g., solar photoconversion, photodetectors, LEDs, biological imaging). With these goals in mind, doping and alloying with Group III, IV, and V elements may play a major role in tailoring the NC properties, such as developing n-type and p-type conductivity through substitutional doping, as well as affecting the optical absorption, emission, and overall charge transport in a NC film. Here we present an extension of the mixed-valence iodide precursor methodology to incorporate Group III, IV, and V elements to produce E-GeNC materials. All main-group elements (E) that surround Ge on the periodic table (i.e., E = Al, Si, P, Ga, As, In, Sn, and Sb) can be incorporated via this methodology. The extent to which the dopant elements are included will be discussed, along with the optical absorbance, emission, and related properties of the NCs. In addition, the effect of the dopant elements on the NC growth kinetics will be discussed.

  14. Performance of a beryllium copper nonmagnetic drill collar alloy

    SciTech Connect

    Dunlevey, F.

    1986-12-01

    Laboratory characterization and extensive field service show the advantages of beryllium copper Brush Alloy 25 for use in nonmagnetic drill collars (NMDC)'s, stabilizers, and subs. Beryllium copper is resistant to stress-corrosion-cracking (SCC) failures at elevated temperatures and pressures in the presence of H/sub 2/S and dissolved chloride solutions. The alloy is more resistant than stainless steel to galling failure in threaded joints. Its magnetic permeability is lower than stainless steel and is unaffected by service conditions.

  15. Electrochemical characteristics of bioresorbable binary MgCa alloys in Ringer's solution: Revealing the impact of local pH distributions during in-vitro dissolution.

    PubMed

    Mareci, D; Bolat, G; Izquierdo, J; Crimu, C; Munteanu, C; Antoniac, I; Souto, R M

    2016-03-01

    Biodegradable magnesium-calcium (MgCa) alloy is a very attractive biomaterial. Two MgCa alloys below the solid solubility of Ca were considered, as to solely investigate the effect of Ca content on the behavior of magnesium and the pH changes associated to metal dissolution. X-ray diffraction analysis and optical microscopy showed that both Mg-0.63Ca and Mg-0.89Ca alloys were solely composed of α(Mg) phase. Degradation characteristics and electrochemical characterization of MgCa alloys were investigated during exposure to Ringer's solution at 37 °C by electrochemical impedance spectroscopy and scanning electrochemical microscopy. The impedance behavior showed both capacitive and inductive features that are related to the alloy charge transfer reaction and the relaxation of the absorbed corrosion compounds, and can be described in terms of an equivalent circuit. Scanning electron microscopy (SEM) was employed to view the surface morphology of the MgCa samples after 1 week immersion in Ringer's solution showing extensive precipitation of corrosion products, whereas the substrate shows evidence of a non-uniform corrosion process. Energy dispersive analysis showed that the precipitates contained oxygen, calcium, magnesium and chlorine, and the Mg:Ca ratios were smaller than in the alloys. Scanning electrochemical microscopy (SECM) was used to visualize local pH changes associated to these physicochemical processes with high spatial resolution. The occurrence of pH variations in excess of 3 units between anodic and cathodic half-cell reactions was monitored in situ.

  16. Performance of NiB inhibitor for PbSCC of alloy 600 in Pb-contaminated water and caustic solutions

    NASA Astrophysics Data System (ADS)

    Kim, Joung Soo; Yi, Yong-Sun; Kwon, Oh Chul; Kim, Mi-Ae; Kim, Hong Pyo

    2008-06-01

    Nickel-based iron-chromium alloys are used as steam generator (SG) tubing materials in nuclear power plants (NPPs) but experience intergranular stress corrosion cracking (IGSCC) and lead stress corrosion cracking (PbSCC) due to the harsh operating conditions of NPPs. In order to improve the integrity of SGs, many studies have sought suitable inhibitors for IGSCC, while those for PbSCC have been sought to a limited extent. In this study, the performance of nickel boride (NiB) as an inhibitor for PbSCC was evaluated. Nickel boride has been shown to be a good inhibitor for IGSCC of Alloy (or Inconel) 600 in a caustic aqueous solution containing no lead (Pb). No significant SCC was observed to occur in Alloy 600 tested in pure water under the slow strain rate test (SSRT) condition in this study. A mixed mode of IGSCC and TGSCC, however, occurred relatively easily in Alloy 600 tested in pure water containing lead oxide (PbO) at 315 °C. The susceptibility of Alloy 600 to SCC decreased with the addition of NiB, implying that NiB can be used as an inhibitor for PbSCC in Pb-contaminated water.

  17. Corrosion resistance of ZrTi alloys with hydroxyapatite-zirconia-silver layer in simulated physiological solution containing proteins for biomaterial applications

    NASA Astrophysics Data System (ADS)

    Mareci, D.; Trincă, L. C.; Căilean, D.; Souto, R. M.

    2016-12-01

    The degradation characteristics of hydroxyapatite-zirconia-silver films (HA-ZrO2-Ag) coatings on three ZrTi alloys were investigated in Ringer's solution containing 10% human albumin protein at 37 °C. Samples were immersed for 7 days while monitored by electrochemical impedance spectroscopy (EIS) and linear potentiodynamic polarization (LPP). The electrochemical analysis in combination with surface analytical characterization by scanning electron microscopy (SEM/EDX) reveals the stability and corrosion resistance of the HA-ZrO2-Ag coated ZrTi alloys. The characteristic feature that describes the electrochemical behaviour of the coated alloys is the coexistence of large areas of the coating presenting pores in which the ZrTi alloy substrate is exposed to the simulated physiological environment. The EIS interpretation of results was thus performed using a two-layer model of the surface film. The blocking effect in the presence the human albumin protein produces an enhancement of the corrosion resistance. The results disclose that the Zr45Ti alloy is a promising material for biomedical devices, since electrochemical stability is directly associated to biocompatibility.

  18. Inhibition of corrosion of Al 6061, aluminum, and an aluminum-copper alloy in chloride-free aqueous media. Part 2: Behavior in basic solutions

    SciTech Connect

    Al-Kharafi, F.M.; Badawy, W.A.

    1998-05-01

    Electrochemical characteristics of Al 6061 (UNS A96061), Al and an Al-Cu alloy were investigated in aqueous solutions. Inhibition of the corrosion processes in basic solutions was studied using electrochemical impedance spectroscopy (EIS) and polarization techniques. Among a series of inhibitors, molybdate (MoO{sub 4}{sup 2{minus}}) and dichromates (Cr{sub 2}O{sub 7}{sup 2{minus}}) were found effective in passivating the metal or alloy surface. The high inhibition action of Cr{sub 2}O{sub 7}{sup 2{minus}} was traced and discussed. X-ray photoelectron spectroscopy (XPS) of the different electrode materials revealed the presence of Cu peaks on the Al-Cu alloy surface. Immersion of the different electrodes in basic solutions containing the same concentration of Cr{sub 2}O{sub 7}{sup 2{minus}}, MoO{sub 4}{sup 2{minus}}, and sulfate (SO{sub 4}{sup 2{minus}}) anions did not show characteristic peaks of Cr, Mo, or S, which meant the surface layer consisted mainly of aluminum oxide (Al{sub 2}O{sub 3}). Depth profiling experiments up to 6.0-nm thickness showed the Cu peaks of the Al-Cu alloy appeared after etching and that Mo was incorporated in the surface film. The presence of Cu on the Al-Cu surface initiated flawed regions, identified by scanning electron microscopy, which were responsible for increased corrosion rates of this alloy. Effectiveness of the dichromate as a corrosion inhibitor for these materials resulted from its powerful oxidizing properties, which led to formation of a stable passive film.

  19. Atomic displacement in the CrMnFeCoNi high-entropy alloy - A scaling factor to predict solid solution strengthening

    NASA Astrophysics Data System (ADS)

    Okamoto, Norihiko L.; Yuge, Koretaka; Tanaka, Katsushi; Inui, Haruyuki; George, Easo P.

    2016-12-01

    Although metals strengthened by alloying have been used for millennia, models to quantify solid solution strengthening (SSS) were first proposed scarcely seventy years ago. Early models could predict the strengths of only simple alloys such as dilute binaries and not those of compositionally complex alloys because of the difficulty of calculating dislocation-solute interaction energies. Recently, models and theories of SSS have been proposed to tackle complex high-entropy alloys (HEAs). Here we show that the strength at 0 K of a prototypical HEA, CrMnFeCoNi, can be scaled and predicted using the root-mean-square atomic displacement, which can be deduced from X-ray diffraction and first-principles calculations as the isotropic atomic displacement parameter, that is, the average displacements of the constituent atoms from regular lattice positions. We show that our approach can be applied successfully to rationalize SSS in FeCoNi, MnFeCoNi, MnCoNi, MnFeNi, CrCoNi, CrFeCoNi, and CrMnCoNi, which are all medium-entropy subsets of the CrMnFeCoNi HEA.

  20. Effects of Solute and Second-Phase Particles on the Texture of Nd-Containing Mg Alloys

    NASA Astrophysics Data System (ADS)

    Hadorn, Jason P.; Hantzsche, Kerstin; Yi, Sangbong; Bohlen, Jan; Letzig, Dietmar; Agnew, Sean R.

    2012-04-01

    Hot-rolled, binary Mg-Nd alloys with compositions ≥0.095 at. pct undergo the texture weakening phenomenon that has been reported in a number of Mg-rare earth (RE) alloys. However, alloys with compositions ≤0.01 at. pct retain a strong basal texture typical of pure Mg and other Mg alloys. Measurements of intragranular misorientation axes obtained using electron backscatter diffraction (EBSD) show that more dilute alloys contain predominantly basal < a > dislocations, while richer alloys contain primarily prismatic < a > dislocations. It is suggested that this change in dislocation content is related to a change in the dynamic recrystallization (DRX) mechanism. Metastable second-phase Mg x Nd1- x intermetallic particles are present within the alloys, and an annealing study indicates that the alloys undergoing texture weakening have grain sizes well predicted by classical Zener drag theory. Even though the more dilute alloys also contain second-phase particles, they are not sufficient to induce pinning. The promotion of nonbasal slip and the reduction in grain boundary mobility due to Zener drag are suggested as controlling mechanisms that promote the observed texture weakening phenomena.

  1. Effect of solution treatment on the fatigue behavior of an as-forged Mg-Zn-Y-Zr alloy

    PubMed Central

    Wang, S. D.; Xu, D. K.; Wang, B. J.; Han, E. H.; Dong, C.

    2016-01-01

    Through investigating and comparing the fatigue behavior of an as-forged Mg-6.7Zn-1.3Y-0.6Zr (wt.%) alloy before and after solid solution treatment (T4) in laboratory air, the effect of T4 treatment on fatigue crack initiation was disclosed. S-N curves illustrated that the fatigue strength of as-forged samples was 110 MPa, whereas the fatigue strength of T4 samples was only 80 MPa. Observations to fracture surfaces demonstrated that for as-forged samples, fatigue crack initiation sites were covered with a layer of oxide film. However, due to the coarse grain structure and the dissolution of MgZn2 precipitates, the activation and accumulation of {10–12} twins in T4 samples were much easier, resulting in the preferential fatigue crack initiation at cracked twin boundaries (TBs). Surface characterization demonstrated that TB cracking was mainly ascribed to the incompatible plastic deformation in the twinned area and nearby α-Mg matrix. PMID:27032532

  2. A Synthetic Pseudo-Rh: NOx Reduction Activity and Electronic Structure of Pd-Ru Solid-solution Alloy Nanoparticles.

    PubMed

    Sato, Katsutoshi; Tomonaga, Hiroyuki; Yamamoto, Tomokazu; Matsumura, Syo; Zulkifli, Nor Diana Binti; Ishimoto, Takayoshi; Koyama, Michihisa; Kusada, Kohei; Kobayashi, Hirokazu; Kitagawa, Hiroshi; Nagaoka, Katsutoshi

    2016-06-24

    Rh is one of the most important noble metals for industrial applications. A major fraction of Rh is used as a catalyst for emission control in automotive catalytic converters because of its unparalleled activity toward NOx reduction. However, Rh is a rare and extremely expensive element; thus, the development of Rh alternative composed of abundant elements is desirable. Pd and Ru are located at the right and left of Rh in the periodic table, respectively, nevertheless this combination of elements is immiscible in the bulk state. Here, we report a Pd-Ru solid-solution-alloy nanoparticle (PdxRu1-x NP) catalyst exhibiting better NOx reduction activity than Rh. Theoretical calculations show that the electronic structure of Pd0.5Ru0.5 is similar to that of Rh, indicating that Pd0.5Ru0.5 can be regarded as a pseudo-Rh. Pd0.5Ru0.5 exhibits better activity than natural Rh, which implies promising applications not only for exhaust-gas cleaning but also for various chemical reactions.

  3. Significant improvement in photoluminescence of ZnSe(S) alloyed quantum dots prepared in high pH solution.

    PubMed

    Zan, Feng; Ren, Jicun

    2010-01-01

    In this paper, we described a simple approach for aqueous synthesis of highly luminescent ZnSe(S) alloyed quantum dots (QDs) in the presence of 3-mercaptopropionic acid as stabilizers using zinc chloride and NaHSe as precursors. The synthesis conditions were systematically investigated. We observed that the pH value of the Zn precursor solution had significant influence on the optical properties and the structure of the as-prepared ZnSe(S) QDs. The optimal pH value and molar ratio of Zn(2+) to HSe(-) were 12.0 and 25 : 1 respectively. Under the optimal conditions, we prepared highly photoluminescent ZnSe(S) QDs at up to 31% quantum yield (compared with Rhodamine 6G). The characterization of HRTEM and XRD showed that the ZnSe(S) QDs had good monodispersity and nice crystal structure. The fluorescence life time spectra demonstrated that ZnSe(S) QDs had a long lifetime in contrast to fluorescent dyes. Compared with the currently used organometallic approach, our method was 'green', the reaction condition was mild and the as-prepared ZnSe(S) QDs were water-soluble. More importantly, our method was low cost, and was very suitable for large-scale synthesis of highly luminescent ZnSe(S) QDs for the future applications. Copyright © 2009 John Wiley & Sons, Ltd.

  4. Growth, microstructure and mechanical properties of microarc oxidation coatings on titanium alloy in phosphate-containing solution

    NASA Astrophysics Data System (ADS)

    Wang, Yaming; Lei, Tingquan; Jiang, Bailing; Guo, Lixin

    2004-06-01

    Ceramic coatings were fabricated by microarc oxidation in galvanostatic regime on Ti6Al4V alloy in (NaPO 3) 6-NaF-NaAlO 2 solution. The growth, microstructure and phase composition of coatings were investigated using scanning electron microscope and X-ray diffraction. With increasing treatment duration, coating growth varies from rapidness to tardiness accompanied by gradually roughening in appearance. Meanwhile, phase transformation of anatase to rutile occurs. The crystalline AlPO 4 is involved in the coatings via high-temperature thermolysis of hydrated aluminium polyphosphates in the nearby discharging channels. The stepped current regime enables coating structure to be controllable. The mechanical properties distribution across the coating thickness and the adhesion strength were determined by nanoindentation and shear test, respectively. A similar evolution profile of hardness and elastic modulus across the coating thickness is found: remaining high values (5.5 and 69.1 GPa) in the compact region before finally declining to low values (5.1 and 65.6 GPa) in the looser region. The adhesion strength of substrate/coating interface is about 40 MPa.

  5. Tribological Properties of Ti-Based Alloys in a Simulated Bone-Implant Interface with Ringer's Solution at Fretting Contacts

    PubMed Central

    Ramos-Saenz, C.R.; Sundaram, P.A.; Diffoot-Carlo, N.

    2010-01-01

    The wear properties of oxidized and non-oxidized gamma-TiAl (a potential biomaterial) as well as Ti-6Al-4V and CP-Ti disks were studied and characterized by means of standard wear tests using a custom made bone pin arrangement. The Ti-base disks were oxidized in air at 500°C and 800°C for one hour. The tribological properties of the oxides formed over the disks were studied using a linear reciprocating wear testing machine under both dry and simulated biological conditions using Ringer's solution. Loss of metal oxide and coefficient of friction values were determined from the wear testing. From the results, abrasion and adhesion were the primary wear mechanisms in each of the three alloy-bone pairs. Specifically, the oxide formed on gamma-TiAl possessed the highest COF and wear resistance of the three materials which were studied. Also, as expected, bone wears down faster than the Ti-base metal oxide. PMID:20826360

  6. Micromechanical Behavior of Solid-Solution-Strengthened Mg-1wt.%Al Alloy Investigated by In-Situ Neutron Diffraction

    SciTech Connect

    Lee, Sooyeol; Woo, Wanchuck; Gharghouri, Michael; Yoon, Cheol; An, Ke

    2014-01-01

    In-situ neutron-diffraction experiments were employed to investigate the micromechanical behavior of solid-solution-strengthened Mg-1wt.%Al alloy. Two starting textures were used: 1) as-extruded then solutionized texture, T1, in which the basal poles of most grains are tilted around 70~85 from the extrusion axis, and 2) a reoriented texture, T2, in which the basal poles of most grains are tilted around 10~20 from the extrusion axis. Lattice strains and diffraction peak intensity variations were measured in situ during loading-unloading cycles in uniaxial tension. Twinning activities and stress states for various grain orientations were revealed. The results show that the soft grain orientations, favorably oriented for either extension twinning or basal slip, exhibit the stress relaxation, resulting in the compressive residual strain after unloading. On the other hand, the hard grain orientations, unfavorably oriented for both extension twinning and basal slip, carry more applied load, leading to much higher lattice strains during loading followed by tensile residual strains upon unloading.

  7. Effect of solution treatment on the fatigue behavior of an as-forged Mg-Zn-Y-Zr alloy

    NASA Astrophysics Data System (ADS)

    Wang, S. D.; Xu, D. K.; Wang, B. J.; Han, E. H.; Dong, C.

    2016-04-01

    Through investigating and comparing the fatigue behavior of an as-forged Mg-6.7Zn-1.3Y-0.6Zr (wt.%) alloy before and after solid solution treatment (T4) in laboratory air, the effect of T4 treatment on fatigue crack initiation was disclosed. S-N curves illustrated that the fatigue strength of as-forged samples was 110 MPa, whereas the fatigue strength of T4 samples was only 80 MPa. Observations to fracture surfaces demonstrated that for as-forged samples, fatigue crack initiation sites were covered with a layer of oxide film. However, due to the coarse grain structure and the dissolution of MgZn2 precipitates, the activation and accumulation of {10–12} twins in T4 samples were much easier, resulting in the preferential fatigue crack initiation at cracked twin boundaries (TBs). Surface characterization demonstrated that TB cracking was mainly ascribed to the incompatible plastic deformation in the twinned area and nearby α-Mg matrix.

  8. A Synthetic Pseudo-Rh: NOx Reduction Activity and Electronic Structure of Pd–Ru Solid-solution Alloy Nanoparticles

    PubMed Central

    Sato, Katsutoshi; Tomonaga, Hiroyuki; Yamamoto, Tomokazu; Matsumura, Syo; Zulkifli, Nor Diana Binti; Ishimoto, Takayoshi; Koyama, Michihisa; Kusada, Kohei; Kobayashi, Hirokazu; Kitagawa, Hiroshi; Nagaoka, Katsutoshi

    2016-01-01

    Rh is one of the most important noble metals for industrial applications. A major fraction of Rh is used as a catalyst for emission control in automotive catalytic converters because of its unparalleled activity toward NOx reduction. However, Rh is a rare and extremely expensive element; thus, the development of Rh alternative composed of abundant elements is desirable. Pd and Ru are located at the right and left of Rh in the periodic table, respectively, nevertheless this combination of elements is immiscible in the bulk state. Here, we report a Pd–Ru solid-solution-alloy nanoparticle (PdxRu1-x NP) catalyst exhibiting better NOx reduction activity than Rh. Theoretical calculations show that the electronic structure of Pd0.5Ru0.5 is similar to that of Rh, indicating that Pd0.5Ru0.5 can be regarded as a pseudo-Rh. Pd0.5Ru0.5 exhibits better activity than natural Rh, which implies promising applications not only for exhaust-gas cleaning but also for various chemical reactions. PMID:27340099

  9. Fatigue property of a bioabsorbable magnesium alloy with a hydroxyapatite coating formed by a chemical solution deposition.

    PubMed

    Hiromoto, Sachiko; Tomozawa, Masanari; Maruyama, Norio

    2013-09-01

    A hydroxyapatite (HAp) coating was directly formed on an extruded AZ31 magnesium alloy by a single-step chemical solution deposition. The HAp coating consists of an outer porous HAp layer, an inner continuous HAp layer, and a thin intermediate MgO layer, and the inner HAp and MgO layers are composed of nanocrystals. Tensile and fatigue tests were performed on the HAp-coated AZ31 in air. The HAp coating microscopically showed neither crack nor detachment at 5% static elongation (1.5% residual strain). With further elongation under tensile stress, cracks were formed perpendicularly to the tensile direction, and fragments of the coating detached with a fracture inside the inner continuous HAp layer. The fatigue strengths at 10(7) cycles (fatigue limit) of HAp-coated and mechanically polished AZ31 were ca. 80 MPa and ca. 90 MPa, respectively. The slight decrease in the fatigue limit with the HAp coating is attributed to small pits with a depth of ca. 10 μm formed on the substrate during the HAp-coating treatment. The HAp coating remained on the specimen without cracks after 10(7) cycles at the fatigue limit, which provides ca. 3% cyclic elongation. Copyright © 2013 Elsevier Ltd. All rights reserved.

  10. A Synthetic Pseudo-Rh: NOx Reduction Activity and Electronic Structure of Pd-Ru Solid-solution Alloy Nanoparticles

    NASA Astrophysics Data System (ADS)

    Sato, Katsutoshi; Tomonaga, Hiroyuki; Yamamoto, Tomokazu; Matsumura, Syo; Zulkifli, Nor Diana Binti; Ishimoto, Takayoshi; Koyama, Michihisa; Kusada, Kohei; Kobayashi, Hirokazu; Kitagawa, Hiroshi; Nagaoka, Katsutoshi

    2016-06-01

    Rh is one of the most important noble metals for industrial applications. A major fraction of Rh is used as a catalyst for emission control in automotive catalytic converters because of its unparalleled activity toward NOx reduction. However, Rh is a rare and extremely expensive element; thus, the development of Rh alternative composed of abundant elements is desirable. Pd and Ru are located at the right and left of Rh in the periodic table, respectively, nevertheless this combination of elements is immiscible in the bulk state. Here, we report a Pd-Ru solid-solution-alloy nanoparticle (PdxRu1-x NP) catalyst exhibiting better NOx reduction activity than Rh. Theoretical calculations show that the electronic structure of Pd0.5Ru0.5 is similar to that of Rh, indicating that Pd0.5Ru0.5 can be regarded as a pseudo-Rh. Pd0.5Ru0.5 exhibits better activity than natural Rh, which implies promising applications not only for exhaust-gas cleaning but also for various chemical reactions.

  11. Effect of solution treatment on the fatigue behavior of an as-forged Mg-Zn-Y-Zr alloy.

    PubMed

    Wang, S D; Xu, D K; Wang, B J; Han, E H; Dong, C

    2016-04-01

    Through investigating and comparing the fatigue behavior of an as-forged Mg-6.7Zn-1.3Y-0.6Zr (wt.%) alloy before and after solid solution treatment (T4) in laboratory air, the effect of T4 treatment on fatigue crack initiation was disclosed. S-N curves illustrated that the fatigue strength of as-forged samples was 110 MPa, whereas the fatigue strength of T4 samples was only 80 MPa. Observations to fracture surfaces demonstrated that for as-forged samples, fatigue crack initiation sites were covered with a layer of oxide film. However, due to the coarse grain structure and the dissolution of MgZn2 precipitates, the activation and accumulation of {10-12} twins in T4 samples were much easier, resulting in the preferential fatigue crack initiation at cracked twin boundaries (TBs). Surface characterization demonstrated that TB cracking was mainly ascribed to the incompatible plastic deformation in the twinned area and nearby α-Mg matrix.

  12. Microstructure and corrosion behavior of binary titanium alloys with beta-stabilizing elements.

    PubMed

    Takada, Y; Nakajima, H; Okuno, O; Okabe, T

    2001-03-01

    Binary titanium alloys with the beta-stabilizing elements of Co, Cr, Cu, Fe, Mn and Pd (up to 30%) and Ag (up to 45%) were examined through metallographic observation and X-ray diffractometry to determine whether beta phases that are advantageous for dental use could be retained. Corrosion behavior was also investigated electrochemically and discussed thermodynamically. Some cast alloys with Co, Cr, Fe, Mn, and Pd retained the beta phase, whereas those with Ag and Cu had no beta phase. In some alloys, an intermetallic compound formed, based on information from the phase diagram. The corrosion resistance deteriorated in the TiAg alloys because Ti2Ag and/or TiAg intermetallic compounds preferentially dissolved in 0.9% NaCl solution. On the other hand, the remaining titanium alloys became easily passive and revealed good corrosion resistance similar to pure titanium since their matrices seemed to thermodynamically form titanium oxides as did pure titanium.

  13. Microstructure and mechanical properties of the as-cast Mg-Zn-Mn-Ca alloys

    NASA Astrophysics Data System (ADS)

    Fu, Junjian; Liu, Ke; Du, Wenbo; Wang, Zhaohui; Li, Shubo; Du, Xian

    2017-03-01

    As-cast Mg-Zn-Mn-Ca alloys are the candidates for medical implants. The microstructure and mechanical properties of the as-cast Mg-Zn-Mn-Ca alloys were investigated by using optical microscope (OM), X-ray diffraction (XRD) and scanning electron microscope (SEM). The results suggested that the addition of Zn significantly refined the grain size of the as-cast magnesium alloys, and hence improved the mechanical properties of the alloys. Meanwhile, the secondary phase mainly distributed in the grain boundaries and the solution treatment made parts of secondary phases dissolved into the matrix, resulting in enhancement of the plasticity of the as-cast Mg-Zn-Mn-Ca alloy.

  14. Formation of Solution-derived Hydroxyapatite Coatings on Titanium Alloy in the Presence of Magnetron-sputtered Alumina Bond Coats.

    PubMed

    Zykova, Anna; Safonov, Vladimir; Yanovska, Anna; Sukhodub, Leonid; Rogovskaya, Renata; Smolik, Jerzy; Yakovin, Stas

    2015-01-01

    Hydroxyapatite Ca10(PO4)6(OH)2 (HAp) and calcium phosphate ceramic materials and coatings are widely used in medicine and dentistry because of their ability to enhance the tissue response to implant surfaces and promote bone ingrowth and osseoconduction processes. The deposition conditions have a great influence on the structure and biofunctionality of calcium phosphate coatings. Corrosion processes and poor adhesion to substrate material reduce the lifetime of implants with calcium phosphate coatings. The research has focused on the development of advanced methods to deposit double-layered ceramic oxide/calcium phosphate coatings by a hybrid technique of magnetron sputtering and thermal methods. The thermal method can promote the crystallization and the formation of HAp coatings on titanium alloy Ti6Al4V substrates at low temperature, based on the principle that the solubility of HAp in aqueous solutions decreases with increasing substrate temperature. By this method, hydroxyapatite directly coated the substrate without precipitation in the initial solution. Using a thermal substrate method, calcium phosphate coatings were prepared at substrate temperatures of 100-105 (o)C. The coated metallic implant surfaces with ceramic bond coats and calcium phosphate layers combine the excellent mechanical properties of metals with the chemical stability of ceramic materials. The corrosion test results show that the ceramic oxide (alumina) coatings and the double-layered alumina-calcium phosphate coatings improve the corrosion resistance compared with uncoated Ti6Al4V and single-layered Ti6Al4V/calcium phosphate substrates. In addition, the double-layered alumina/hydroxyapatite coatings demonstrate the best biocompatibility during in vitro tests.

  15. Formation of Solution-derived Hydroxyapatite Coatings on Titanium Alloy in the Presence of Magnetron-sputtered Alumina Bond Coats

    PubMed Central

    Zykova, Anna; Safonov, Vladimir; Yanovska, Anna; Sukhodub, Leonid; Rogovskaya, Renata; Smolik, Jerzy; Yakovin, Stas

    2015-01-01

    Hydroxyapatite Ca10(PO4)6(OH)2 (HAp) and calcium phosphate ceramic materials and coatings are widely used in medicine and dentistry because of their ability to enhance the tissue response to implant surfaces and promote bone ingrowth and osseoconduction processes. The deposition conditions have a great influence on the structure and biofunctionality of calcium phosphate coatings. Corrosion processes and poor adhesion to substrate material reduce the lifetime of implants with calcium phosphate coatings. The research has focused on the development of advanced methods to deposit double-layered ceramic oxide/calcium phosphate coatings by a hybrid technique of magnetron sputtering and thermal methods. The thermal method can promote the crystallization and the formation of HAp coatings on titanium alloy Ti6Al4V substrates at low temperature, based on the principle that the solubility of HAp in aqueous solutions decreases with increasing substrate temperature. By this method, hydroxyapatite directly coated the substrate without precipitation in the initial solution. Using a thermal substrate method, calcium phosphate coatings were prepared at substrate temperatures of 100-105 oC. The coated metallic implant surfaces with ceramic bond coats and calcium phosphate layers combine the excellent mechanical properties of metals with the chemical stability of ceramic materials. The corrosion test results show that the ceramic oxide (alumina) coatings and the double-layered alumina-calcium phosphate coatings improve the corrosion resistance compared with uncoated Ti6Al4V and single-layered Ti6Al4V/calcium phosphate substrates. In addition, the double-layered alumina/hydroxyapatite coatings demonstrate the best biocompatibility during in vitro tests. PMID:25893018

  16. Influence of surface modification of nitinol with silicon using plasma-immersion ion implantation on the alloy corrosion resistance in artificial physiological solutions

    NASA Astrophysics Data System (ADS)

    Kashin, O. A.; Borisov, D. P.; Lotkov, A. I.; Abramova, P. V.; Korshunov, A. V.

    2015-10-01

    Cyclic voltammetry and potentiostatic polarization have been applied to study electrochemical behavior and to determine corrosion resistance of nitinol, which surface was modified with silicon using plasma-immersion ion implantation, in 0.9% NaCl solution and in artificial blood plasma. It was found out that continuous, and also homogeneous in composition, thin Si-containing layers are resistant to corrosion damage at high positive potentials in artificial physiological solutions due to formation of stable passive films. Breakdown potential Eb of Si-modified NiTi depends on the character of silicon and Ni distribution at the alloy surface, Eb values amounted to 0.9-1.5 V (Ag/AgCl/KCl sat.) for the alloy samples with continuous Si-containing surface layers and with decreased Ni surface concentration.

  17. Progress in dissolving modified LEU Cintichem targets

    SciTech Connect

    Leonard, R.A.; Chen, L.; Mertz, C.J.; Vandegrift, G.F.

    1996-12-31

    A process is under development to use low-enriched uranium (LEU) metal targets for production of {sup 99}Mo. The first step is to dissolve the irradiated foil. In past work, this has been done by heating a closed (sealed) vessel containing the foil and a solution of nitric and sulfuric acids. In this work, the authors have demonstrated that (1) the dissolver solution can contain nitric acid alone, (2) uranium dioxide is also dissolved by nitric acid alone, and (3) barrier metals of Cu, Fe, or Ni on the U foil are also dissolved by nitric acid. Changes to the dissolver design and operation needed to accommodate the uranium foil are discussed, including (1) simple operations that are easy to do in a remote-maintenance facility, (2) heat removal from the irradiated LEU foil, and (3) cold trap operation with high dissolver pressures.

  18. A Practical Anodic and Cathodic Curve Intersection Model to Understand Multiple Corrosion Potentials of Fe-Based Glassy Alloys in OH- Contained Solutions.

    PubMed

    Li, Y J; Wang, Y G; An, B; Xu, H; Liu, Y; Zhang, L C; Ma, H Y; Wang, W M

    2016-01-01

    A practical anodic and cathodic curve intersection model, which consisted of an apparent anodic curve and an imaginary cathodic line, was proposed to explain multiple corrosion potentials occurred in potentiodynamic polarization curves of Fe-based glassy alloys in alkaline solution. The apparent anodic curve was selected from the measured anodic curves. The imaginary cathodic line was obtained by linearly fitting the differences of anodic curves and can be moved evenly or rotated to predict the number and value of corrosion potentials.

  19. Fatigue Crack Growth Rates of High-Magnesium Aluminum-Magnesium Alloys as Influenced by Solution Treatment Time and Alloy Content.

    DTIC Science & Technology

    1983-06-01

    Society for Metals, 1979. 6. American Society of Metals , Metals Handbook, Ninth Edition, Volume 2, Properties and Selection of Non Ferrous Alloys and...Aircraft Establish- ment, Farnbough, Hants., England October 1981. 8. American Society of Metals , Metals Handbook, Ninth Edition, Volume 2

  20. Formation of one-dimensional Ag-Au solid solution colloids with Au nanorods as seeds, their alloying mechanisms, and surface plasmon resonances

    NASA Astrophysics Data System (ADS)

    Guo, Tao; Tan, Yiwei

    2012-12-01

    In this work, one dimensional (1D) Ag-Au solid solution nanoalloys were synthesized by rapidly diffusing Ag into the preformed Au nanorod (AuNR) seeds at ambient temperature in aqueous solution. By varying the molar ratio of AgCl/AuNR (in gold atoms), two kinds of 1D Ag-Au alloy nanostructures with a narrow size distribution--AgAu nanowires and Ag33Au67 nanorods--could be obtained in high yields when NaCl and polyvinylpyrrolidone (PVP) were used as an additive and capping reagent, respectively. Based on HRTEM imaging combined with a series of control experiments, it is conceivable that vacancy/defect-motivated interdiffusion of Ag and Au atoms coupled with oxidative etching is a crucial stage in the mechanism responsible for this room-temperature alloying process, and the subsequent conjugation of the fused Ag-Au alloyed nanostructures is associated with the formation of the AgAu nanowires. The resulting 1D Ag-Au nanoalloys form stable colloidal dispersions and show unique localized surface plasmon resonance (LSPR) peaks in the ensemble extinction spectra.In this work, one dimensional (1D) Ag-Au solid solution nanoalloys were synthesized by rapidly diffusing Ag into the preformed Au nanorod (AuNR) seeds at ambient temperature in aqueous solution. By varying the molar ratio of AgCl/AuNR (in gold atoms), two kinds of 1D Ag-Au alloy nanostructures with a narrow size distribution--AgAu nanowires and Ag33Au67 nanorods--could be obtained in high yields when NaCl and polyvinylpyrrolidone (PVP) were used as an additive and capping reagent, respectively. Based on HRTEM imaging combined with a series of control experiments, it is conceivable that vacancy/defect-motivated interdiffusion of Ag and Au atoms coupled with oxidative etching is a crucial stage in the mechanism responsible for this room-temperature alloying process, and the subsequent conjugation of the fused Ag-Au alloyed nanostructures is associated with the formation of the AgAu nanowires. The resulting 1D Ag

  1. Surface alloying of Mg alloys after surface nanocrystallization.

    PubMed

    Zhang, Ming-Xing; Shi, Yi-Nong; Sun, Haiqing; Kelly, Patrick M

    2008-05-01

    Surface nanocrystallization using a surface mechanical attrition treatment effectively activates the surface of magnesium alloys due to the increase in grain boundary diffusion channels. As a result, the temperature of subsequent surface alloying treatment of pure Mg and AZ91 alloy can be reduced from 430 degrees C to 380 degrees C. Thus, it is possible to combine the surface alloying process with the solution treatment for this type of alloy. After surface alloying, the hardness of the alloyed layer is 3 to 4 times higher than that of the substrate and this may significantly improve the wear resistance of magnesium alloys.

  2. Effect of Sintering Atmosphere and Solution Treatment on Density, Microstructure and Tensile Properties of Duplex Stainless Steels Developed from Pre-alloyed Powders

    NASA Astrophysics Data System (ADS)

    Murali, Arun Prasad; Mahendran, Sudhahar; Ramajayam, Mariappan; Ganesan, Dharmalingam; Chinnaraj, Raj Kumar

    2017-10-01

    In this research, Powder Metallurgy (P/M) of Duplex Stainless Steels (DSS) of different compositions were prepared through pre-alloyed powders and elemental powders with and without addition of copper. The powder mix was developed by pot mill for 12 h to obtain the homogeneous mixture of pre-alloyed powder with elemental compositions. Cylindrical green compacts with the dimensions of 30 mm diameter and 12 mm height were compacted through universal testing machine at a pressure level of 560 ± 10 MPa. These green compacts were sintered at 1350 °C for 2 h in hydrogen and argon atmospheres. Some of the sintered stainless steel preforms were solution treated at 1050 °C followed by water quenching. The sintered as well as solution treated samples were analysed by metallography examination, Scanning Electron Microscopy and evaluation of mechanical properties. Ferrite content of sintered and solution treated DSS were measured by Fischer Ferritoscope. It is inferred that the hydrogen sintered DSS depicted better density (94% theoretical density) and tensile strength (695 MPa) than the argon sintered steels. Similarly the microstructure of solution treated DSS revealed existence of more volume of ferrite grains than its sintered condition. Solution treated hydrogen sintered DSS A (50 wt% 316L + 50 wt% 430L) exhibited higher tensile strength of 716 MPa and elongation of 17%, which are 10-13% increment than the sintered stainless steels.

  3. Crystallization and Corrosion Resistance in Different Aqueous Solutions of Zr50.7Ni28Cu9Al12.3 Amorphous Alloy and Its Crystallization Counterparts

    NASA Astrophysics Data System (ADS)

    Ge, Wenjuan; Li, Boyu; Axinte, Eugen; Zhang, Zitang; Shang, Caiyun; Wang, Yan

    2017-02-01

    The Zr50.7Ni28Cu9Al12.3 amorphous alloy and its crystallization counterparts have been prepared using a melt spinning technique and proper annealing treatment. The as-annealed products at 768 K are amorphous composites consisting of a main amorphous phase and a few ZrO2 nanocrystals. The corrosion behaviors have been investigated in 0.5-M NaCl, 1-M HCl, and 0.5-M H2SO4 solutions. The results show that amorphous composites present the enhanced corrosion resistance in Cl- containing solutions due to the formation of compact passive films, which are promoted by an appropriate quantity of ZrO2 nanocrystals. Nevertheless, the relaxed samples possess good corrosion resistance in H2SO4 solution, which is attributed to the existence of Zr(Al, Ni)-rich protective film induced by the depletion of Cu. In addition, corrosion resistance of the tested alloys is relatively superior in H2SO4 solution, especially for pitting corrosion resistance, and inferior in HCl solution.

  4. Crystallization and Corrosion Resistance in Different Aqueous Solutions of Zr50.7Ni28Cu9Al12.3 Amorphous Alloy and Its Crystallization Counterparts

    NASA Astrophysics Data System (ADS)

    Ge, Wenjuan; Li, Boyu; Axinte, Eugen; Zhang, Zitang; Shang, Caiyun; Wang, Yan

    2017-04-01

    The Zr50.7Ni28Cu9Al12.3 amorphous alloy and its crystallization counterparts have been prepared using a melt spinning technique and proper annealing treatment. The as-annealed products at 768 K are amorphous composites consisting of a main amorphous phase and a few ZrO2 nanocrystals. The corrosion behaviors have been investigated in 0.5-M NaCl, 1-M HCl, and 0.5-M H2SO4 solutions. The results show that amorphous composites present the enhanced corrosion resistance in Cl- containing solutions due to the formation of compact passive films, which are promoted by an appropriate quantity of ZrO2 nanocrystals. Nevertheless, the relaxed samples possess good corrosion resistance in H2SO4 solution, which is attributed to the existence of Zr(Al, Ni)-rich protective film induced by the depletion of Cu. In addition, corrosion resistance of the tested alloys is relatively superior in H2SO4 solution, especially for pitting corrosion resistance, and inferior in HCl solution.

  5. Effect of Sintering Atmosphere and Solution Treatment on Density, Microstructure and Tensile Properties of Duplex Stainless Steels Developed from Pre-alloyed Powders

    NASA Astrophysics Data System (ADS)

    Murali, Arun Prasad; Mahendran, Sudhahar; Ramajayam, Mariappan; Ganesan, Dharmalingam; Chinnaraj, Raj Kumar

    2017-01-01

    In this research, Powder Metallurgy (P/M) of Duplex Stainless Steels (DSS) of different compositions were prepared through pre-alloyed powders and elemental powders with and without addition of copper. The powder mix was developed by pot mill for 12 h to obtain the homogeneous mixture of pre-alloyed powder with elemental compositions. Cylindrical green compacts with the dimensions of 30 mm diameter and 12 mm height were compacted through universal testing machine at a pressure level of 560 ± 10 MPa. These green compacts were sintered at 1350 °C for 2 h in hydrogen and argon atmospheres. Some of the sintered stainless steel preforms were solution treated at 1050 °C followed by water quenching. The sintered as well as solution treated samples were analysed by metallography examination, Scanning Electron Microscopy and evaluation of mechanical properties. Ferrite content of sintered and solution treated DSS were measured by Fischer Ferritoscope. It is inferred that the hydrogen sintered DSS depicted better density (94% theoretical density) and tensile strength (695 MPa) than the argon sintered steels. Similarly the microstructure of solution treated DSS revealed existence of more volume of ferrite grains than its sintered condition. Solution treated hydrogen sintered DSS A (50 wt% 316L + 50 wt% 430L) exhibited higher tensile strength of 716 MPa and elongation of 17%, which are 10-13% increment than the sintered stainless steels.

  6. Effects of Fe concentration on the ion-irradiation induced defect evolution and hardening in Ni-Fe solid solution alloys

    DOE PAGES

    Jin, Ke; Guo, Wei; Lu, Chenyang; ...

    2016-12-01

    Understanding alloying effects on the irradiation response of structural materials is pivotal in nuclear engineering. In order to systematically explore the effects of Fe concentration on the irradiation-induced defect evolution and hardening in face-centered cubic Ni-Fe binary solid solution alloys, single crystalline Ni-xFe (x = 0–60 at%) alloys have been grown and irradiated with 1.5 MeV Ni ions. The irradiations have been performed over a wide range of fluences from 3 × 1013 to 3 × 1016 cm-2 at room temperature. Ion channeling technique has shown reduced damage accumulation with increasing Fe concentration in the low fluence regime, which ismore » consistent to the results from molecular dynamic simulations. We did not observe any irradiation-induced compositional segregation in atom probe tomography within the detection limit, even in the samples irradiated with high fluence Ni ions. Transmission electron microscopy analyses have further demonstrated that the defect size significantly decreases with increasing Fe concentration, indicating a delay in defect evolution. Furthermore, irradiation induced hardening has been measured by nanoindentation tests. Ni and the Ni-Fe alloys have largely different initial hardness, but they all follow a similar trend for the increase of hardness as a function of irradiation fluence.« less

  7. Effects of Fe concentration on the ion-irradiation induced defect evolution and hardening in Ni-Fe solid solution alloys

    SciTech Connect

    Jin, Ke; Guo, Wei; Lu, Chenyang; Ullah, Mohammad W.; Zhang, Yanwen; Weber, William J.; Wang, Lumin; Poplawsky, Jonathan D.; Bei, Hongbin

    2016-12-01

    Understanding alloying effects on the irradiation response of structural materials is pivotal in nuclear engineering. In order to systematically explore the effects of Fe concentration on the irradiation-induced defect evolution and hardening in face-centered cubic Ni-Fe binary solid solution alloys, single crystalline Ni-xFe (x = 0–60 at%) alloys have been grown and irradiated with 1.5 MeV Ni ions. The irradiations have been performed over a wide range of fluences from 3 × 1013 to 3 × 1016 cm-2 at room temperature. Ion channeling technique has shown reduced damage accumulation with increasing Fe concentration in the low fluence regime, which is consistent to the results from molecular dynamic simulations. We did not observe any irradiation-induced compositional segregation in atom probe tomography within the detection limit, even in the samples irradiated with high fluence Ni ions. Transmission electron microscopy analyses have further demonstrated that the defect size significantly decreases with increasing Fe concentration, indicating a delay in defect evolution. Furthermore, irradiation induced hardening has been measured by nanoindentation tests. Ni and the Ni-Fe alloys have largely different initial hardness, but they all follow a similar trend for the increase of hardness as a function of irradiation fluence.

  8. Improvement of abrasion resistance in artificial seawater and corrosion resistance in NaCl solution of 7075 aluminum alloy processed by laser shock peening

    NASA Astrophysics Data System (ADS)

    Wang, Hao; Ning, Chengyi; Huang, Yihui; Cao, Zhenya; Chen, Xiaoxiao; Zhang, Wenwu

    2017-03-01

    As 7075 aluminum alloy is widely used in a humid environment, in order to enhance its abrasion resistance and electrochemical corrosion resistance, the paper studied the effect of laser shock peening on abrasion resistance in artificial seawater and corrosion resistance in 3.5% NaCl solution of 7075 aluminum alloy. Result shows that when specimens were treated once and twice with 7.17 GW/cm2 the abrasion loss would be reduced by 43.75% and 46.09% compare to untreated respectively, and the corrosion rate of 7075 aluminum alloy could be reduced as much as 50.32% by LSP treatment with 7.17 GW/cm2. What's more, the effects on the microhardness, microstructure and residual stress with different LSP impacts and power density were investigated to find out strengthening mechanism of laser shock peening, which were observed and measured by microhardness tester, optical microscope and X-ray diffraction (XRD) residual stress tester. In the entire laboratory tests, it is considered that LSP is a practical option to improve abrasion resistance in seawater and corrosion resistance of 7075 aluminum alloy.

  9. Hydrogen interactions in aluminum-lithium alloys

    NASA Technical Reports Server (NTRS)

    Smith, S. W.; Scully, J. R.

    1991-01-01

    A program is described which seeks to develop an understanding of the effects of dissolved and trapped hydrogen on the mechanical properties of selected Al-Li-Cu-X alloys. A proposal is made to distinguish hydrogen (H2) induced EAC from aqueous dissolution controlled EAC, to correlate H2 induced EAC with mobile and trapped concentrations, and to identify significant trap sites and hydride phases (if any) through use of model alloys and phases. A literature review shows three experimental factors which have impeded progress in the area of H2 EAC for this class of alloys. These are as listed: (1) inter-subgranular fracture in Al-Li alloys when tested in the S-T orientation in air or vacuum make it difficult to readily detect H2 induced fracture based on straight forward changes in fractography; (2) the inherently low H2 diffusivity and solubility in Al alloys is further compounded by a native oxide which acts as a H2 permeation barrier; and (3) H2 effects are masked by dissolution assisted processes when mechanical testing is performed in aqueous solutions.

  10. EIS and XPS investigations on the corrosion mechanism of ternary Zn-Co-Mo alloy coatings in NaCl solution

    NASA Astrophysics Data System (ADS)

    Winiarski, J.; Tylus, W.; Szczygieł, B.

    2016-02-01

    The changes in composition of the corrosion products of electrodeposited ternary Zn-Co-Mo alloy coatings on AISI 1015 steel during exposure to 0.5 mol dm-3 NaCl solution were investigated. XPS studies demonstrated that at the initial stage of corrosion on the surface of Zn-Co-Mo coating zinc hydroxide layer is formed. Hydroxyl groups react with chloride and carbonate ions which lead to the formation of zinc hydroxy carbonates and zinc hydroxy chlorides. The share of these compounds in the oxidation products is initially large. However, with time zinc hydroxy compounds slowly changes to zinc oxide, which is more stable corrosion product. It was estimated that after 24 h of exposure to NaCl solution nearly 60% of zinc detected on the surface of Zn-Co-Mo coating was present in the ZnO form, 18% in the form of zinc hydroxy chloride, and more than 21% as zinc hydroxy carbonate. XPS analyses revealed that the amount of zinc hydroxy chloride increases as the exposure time lengthens and it is significantly higher than at the surface of binary Zn-Co coating. The presence of crystalline zinc chloride hydroxide as a stable product of corrosion of ternary Zn-Co-Mo alloy coating in a 0.5 mol dm-3 NaCl solution was confirmed by XRD analysis. According to XRD and FTIR other zinc corrosion products like: ZnO, Zn(OH)2 and Zn5(CO3)2(OH)6 were also present. The results of XPS and EIS measurements allow us to assume that in the presence of Mo in the alloy, on the surface of ternary Zn-Co-Mo alloy (3.4 wt.% Co, 2.7 wt.% Mo) coating more zinc hydroxy chloride is formed, which favors higher corrosion resistance of this coating.

  11. Characterization of low alloy ferritic steel–Ni base alloy dissimilar metal weld interface by SPM techniques, SEM/EDS, TEM/EDS and SVET

    SciTech Connect

    Wang, Siyan; Ding, Jie; Ming, Hongliang; Zhang, Zhiming; Wang, Jianqiu

    2015-02-15

    The interface region of welded A508–Alloy 52 M is characterized by scanning probe microscope (SPM) techniques, scanning electron microscopy (SEM)/energy dispersive spectroscopy (EDS), transmission electron microscopy (TEM)/Energy Dispersive Spectroscopy (EDS) and scanning vibrate electrode technique (SVET). The regions along the welded A508–Alloy 52 M interface can be categorized into two types according to their different microstructures. In the type-I interface region, A508 and Alloy 52 M are separated by the fusion boundary, while in the type-II interface region, A508 and Alloy 52 M are separated by a martensite zone. A508, martensite zone and grain boundaries in Alloy 52 M are ferromagnetic while the Alloy 52 M matrix is paramagnetic. The Volta potentials measured by scanning Kelvin probe force microscopy (SKPFM) of A508, martensite zone and Alloy 52 M follow the order: V{sub 52} {sub M} > V{sub A508} > V{sub martensite}. The corrosion behavior of A508–Alloy 52 M interface region is galvanic corrosion, in which Alloy 52 M is cathode while A508 is anode. The martensite dissolves faster than Alloy 52 M, but slower than A508 in the test solution. - Highlights: • The A508–Alloy 52 M interface regions can be categorized into two types. • The chromium depleted region is observed along the Alloy 52 M grain boundary. • The Alloy 52 M grain boundaries which are close to the interface are ferromagnetic. • Martensite zone has lower Volta potential but higher corrosion resistance than A508.

  12. Electrocatalytic Oxidation of Formic Acid in an Alkaline Solution with Graphene-Oxide- Supported Ag and Pd Alloy Nanoparticles.

    PubMed

    Han, Hyoung Soon; Yun, Mira; Jeong, Haesang; Jeon, Seungwon

    2015-08-01

    The electrocatalytic activities of metal-decorated graphene oxide (GO) catalysts were investigated. Electrochemically reduced GO-S-(CH2)4-S-Pd [ERGO-S-(CH2)4-S-Pd] and GO-S-(CH2)4-S-PdAg alloy [ERGO-S-(CH2)4-S-PdAg] were obtained through the electrochemical reduction of GO-S-(CH2)4-S-Pd and GO-S-(CH2)4-S-PdAg in a pH 5 PBS solution. It was demonstrated that the application of ERGO-S-(CH2)4-S-Pd and ERGO-S-(CH2)4-S-PdAg used in a modified GCE improves the electrocatalytic oxidation of formic acid. The addition of an Ag nanoparticle with a carbon chain-Pd in the electrode provides an electrode with very interesting properties for the electrocatalytic oxidation of formic acid. The ERGO-S-(CH2)4-S-Pd and ERGO-S-(CH2)4-S-PdAg were characterized via X-ray photoelectron spectroscopy (XPS), scanning electron microscopy (SEM) and transmission electron microscopy (TEM). ERGO-S-(CH2)4-S-Pd and ERGO-S-(CH2)4-S-PdAg can be employed for the electrocatalytic oxidation of formic acid. The electrochemical behaviors of this electrode were investigated using cyclic voltammetry (CV), chronoamperometry (CA) and electrochemical impedance spectroscopy (EIS).

  13. Wear transition of solid-solution-strengthened Ti-29Nb-13Ta-4.6Zr alloys by interstitial oxygen for biomedical applications.

    PubMed

    Lee, Yoon-Seok; Niinomi, Mitsuo; Nakai, Masaaki; Narita, Kengo; Cho, Ken; Liu, Huihong

    2015-11-01

    In previous studies, it has been concluded that volume losses (V loss) of the Ti-29Nb-13Ta-4.6Zr (TNTZ) discs and balls are larger than those of the respective Ti-6Al-4V extra-low interstitial (Ti64) discs and balls, both in air and Ringer's solution. These results are related to severe subsurface deformation of TNTZ, which is caused by the lower resistance to plastic shearing of TNTZ than that of Ti64. Therefore, it is necessary to further increase the wear resistance of TNTZ to satisfy the requirements as a biomedical implant. From this viewpoint, interstitial oxygen was added to TNTZ to improve the plastic shear resistance via solid-solution strengthening. Thus, the wear behaviors of combinations comprised of a new titanium alloy, TNTZ with high oxygen content of 0.89 mass% (89O) and a conventional titanium alloy, Ti64 were investigated in air and Ringer's solution for biomedical implant applications. The worn surfaces, wear debris, and subsurface damage were analyzed using a scanning electron microscopy and an electron probe microanalysis. V loss of the 89O discs and balls are smaller than those of the respective TNTZ discs and balls in both air and Ringer's solution. It can be concluded that the solid-solution strengthening by oxygen effectively improves the wear resistance for TNTZ materials. However, the 89O disc/ball combination still exhibits higher V loss than the Ti64 disc/ball combination in both air and Ringer's solution. Moreover, V loss of the disc for the 89O disc/Ti64 ball combination significantly decreases in Ringer's solution compared to that in air. This decrease for the 89O disc/Ti64 ball combination in Ringer's solution can be explained by the transition in the wear mechanism from severe delamination wear to abrasive wear. Copyright © 2015 Elsevier Ltd. All rights reserved.

  14. Formation of one-dimensional Ag-Au solid solution colloids with Au nanorods as seeds, their alloying mechanisms, and surface plasmon resonances.

    PubMed

    Guo, Tao; Tan, Yiwei

    2013-01-21

    In this work, one dimensional (1D) Ag-Au solid solution nanoalloys were synthesized by rapidly diffusing Ag into the preformed Au nanorod (AuNR) seeds at ambient temperature in aqueous solution. By varying the molar ratio of AgCl/AuNR (in gold atoms), two kinds of 1D Ag-Au alloy nanostructures with a narrow size distribution--AgAu nanowires and Ag(33)Au(67) nanorods--could be obtained in high yields when NaCl and polyvinylpyrrolidone (PVP) were used as an additive and capping reagent, respectively. Based on HRTEM imaging combined with a series of control experiments, it is conceivable that vacancy/defect-motivated interdiffusion of Ag and Au atoms coupled with oxidative etching is a crucial stage in the mechanism responsible for this room-temperature alloying process, and the subsequent conjugation of the fused Ag-Au alloyed nanostructures is associated with the formation of the AgAu nanowires. The resulting 1D Ag-Au nanoalloys form stable colloidal dispersions and show unique localized surface plasmon resonance (LSPR) peaks in the ensemble extinction spectra.

  15. Sub-micrometre holotomographic characterisation of the effects of solution heat treatment on an AlMg7.3Si3.5 alloy

    PubMed Central

    Tolnai, D.; Requena, G.; Cloetens, P.; Lendvai, J.; Degischer, H.P.

    2012-01-01

    A strip cast AlMg7.3Si3.5 alloy is investigated by sub-micrometre holotomographic analysis achieving a voxel size of (60 nm)3 by cone beam magnification of the focused synchrotron beam using Kirkpatrick–Baez mirrors. The three-dimensional microstructure of the same specimen volume in the as-cast state is compared with that after exposure to 540 °C for 30 min resolving microstructural features down to 180 nm. The three-dimensional analysis of the architecture of the eutectic Mg2Si and the Fe-aluminides reveals how the as-cast microstructure changes during the solution treatment. The alloy in the as-cast condition contains a highly interconnected seaweed-like Mg2Si eutectic. The level of three-dimensional interconnectivity of the Mg2Si eutectic phase decreases by only partial disintegration during the heat treatment correcting the two-dimensional metallographic impression of isolated round particles. Statistical analyses of the particle distribution, sphericity, mean curvatures and Gaussian curvatures describe quantitatively the architectural changes of the Mg2Si phase. This explains the decrease of the high temperature strength of the alloy by the solution treatment tested in hot compression. PMID:23483521

  16. Influence of surface wettability on the tribological properties of laser textured Co-Cr-Mo alloy in aqueous bovine serum albumin solution

    NASA Astrophysics Data System (ADS)

    Qin, Liguo; Lin, Ping; Zhang, Yali; Dong, Guangneng; Zeng, Qunfeng

    2013-03-01

    Surface wettability behaviors of three kinds of laser textured Co-Cr-Mo alloy surfaces (arrays of circular, triangular and square shape dimples) were evaluated in aqueous bovine serum albumin (BSA) solution. The tribological properties of laser textured Co-Cr-Mo alloy were investigated by pin-on-disc reciprocating tribometer under BSA lubrication. The wetting surfaces ranging from superhydrophilic (CA = 21.5°) to superhydrophobic (CA = 142.2°) were obtained by dual/combined surface modification including laser surface texturing (LST) and further fluoro-alkyl silane (FAS). It was found that surface wettability behaviors of Co-Cr-Mo alloy surfaces were closely related to their tribological behaviors in BSA solution. Results showed that the contact angle of circular dimple was the most stable, sliding time of the friction pair reaching steady state stage was shortest and coefficient of friction was minimum among three regular layout shapes of dimples during the tribological tests. It suggests that the combined surface modification of LST and FAS is a promising method to improve the tribological performances and prolong the service life of Co-Cr-Mo orthopedic implants.

  17. In vitro biocompatibility of Ti-Mg alloys fabricated by direct current magnetron sputtering.

    PubMed

    Hieda, Junko; Niinomi, Mitsuo; Nakai, Masaaki; Cho, Ken

    2015-09-01

    Ti-xMg (x=17, 33, and 55 mass%) alloy films, which cannot be prepared by conventional melting processes owing to the absence of a solid-solution phase in the phase diagram, were prepared by direct current magnetron sputtering in order to investigate their biocompatibility. Ti and Mg films were also prepared by the same process for comparison. The crystal structures were examined by X-ray diffraction (XRD) analysis and the surfaces were analyzed by X-ray photoelectron spectroscopy. The Ti, Ti-xMg alloy, and Mg films were immersed in a 0.9% NaCl solution at 310 K for 7d to evaluate the dissolution amounts of Ti and Mg. In addition, to evaluate the formation ability of calcium phosphate in vitro, the Ti, Ti-xMg alloy, and Mg films were immersed in Hanks' solution at 310 K for 30 d. Ti and Mg form solid-solution alloys because the peaks attributed to pure Ti and Mg do not appear in the XRD patterns of any of the Ti-xMg alloy films. The surfaces of the Ti-17 Mg alloy and Ti-33 Mg alloy films contain Ti oxides and MgO, whereas MgO is the main component of the surface oxide of the Ti-55 Mg alloy and Mg films. The dissolution amounts of Ti from all films are below or near the detection limit of inductively coupled plasma-optical emission spectroscopy. On the other hand, the Ti-17 Mg alloy, Ti-33 Mg alloy, Ti-55 Mg alloy, and Mg films exhibit Mg dissolution amounts of approximately 2.5, 1.4, 21, and 41 μg/cm(2), respectively. The diffraction peaks attributed to calcium phosphate are present in the XRD patterns of the Ti-33 Mg alloy, Ti-55 Mg alloy, and Mg films after the immersion in Hanks' solution. Spherical calcium phosphate particles precipitate on the surface of the Ti-33 Mg film. However, many cracks are observed in the Ti-55 Mg film, and delamination of the film occurs after the immersion in Hanks' solution. The Mg film is dissolved in Hanks' solution and calcium phosphate particles precipitate on the glass substrate. Consequently, it is revealed that the Ti-33 Mg

  18. High strength uranium-tungsten alloy process

    DOEpatents

    Dunn, Paul S.; Sheinberg, Haskell; Hogan, Billy M.; Lewis, Homer D.; Dickinson, James M.

    1990-01-01

    Alloys of uranium and tungsten and a method for making the alloys. The amount of tungsten present in the alloys is from about 4 wt % to about 35 wt %. Tungsten particles are dispersed throughout the uranium and a small amount of tungsten is dissolved in the uranium.

  19. High strength uranium-tungsten alloys

    DOEpatents

    Dunn, Paul S.; Sheinberg, Haskell; Hogan, Billy M.; Lewis, Homer D.; Dickinson, James M.

    1991-01-01

    Alloys of uranium and tungsten and a method for making the alloys. The amount of tungsten present in the alloys is from about 4 wt % to about 35 wt %. Tungsten particles are dispersed throughout the uranium and a small amount of tungsten is dissolved in the uranium.

  20. The mechanism of corrosion of palladium-silver binary alloys in artificial saliva.

    PubMed

    Joska, L; Marek, M; Leitner, J

    2005-05-01

    Palladium dental casting alloys are alternatives to gold alloys. The aim of this study was to determine the electrochemical behaviour and the corrosion mechanism of binary silver-palladium alloys. Seven binary silver-palladium alloys and pure palladium and silver were tested in a model saliva solution. Electrochemical tests included corrosion potential, polarization resistance, and potentiodynamic polarization measurements. The corrosion products, which may be theoretically formed, were determined by thermodynamic calculation. The behaviour of silver and silver-rich alloys was dominated by the preferential formation of a thiocyanate surface layer, which controlled the free corrosion potential. Palladium dissolved in the form of a thiocyanate complex, but the surface became passivated by either palladium oxide or solid palladium thiocyanate layer, the thermodynamic calculations indicating preference for the oxide. Palladium-rich alloys showed evidence of silver depletion of the surface, resulting in behaviour similar to palladium. Examination of binary silver-palladium alloys has made possible determination of the role of the components of the alloys and model saliva in the corrosion behaviour. The findings are applicable to the more complex commercial dental alloys containing silver and palladium as major components.

  1. Facile synthesis of nitrogen-doped carbon nanotubes encapsulating nickel cobalt alloys 3D networks for oxygen evolution reaction in an alkaline solution

    NASA Astrophysics Data System (ADS)

    Yu, Jie; Zhong, Yijun; Zhou, Wei; Shao, Zongping

    2017-01-01

    Efficient oxygen evolution reaction (OER) catalysts are required to facilitate the large-scale exploitation of renewable energy resources and applications in electrochemical energy conversion technologies. Here, we show that metal alloy-based hybrids can provide higher electrocatalytic activity than their individual metal-based hybrids. In particular, NiCo alloys encapsulated within nitrogen-doped carbon nanotubes (NiCo@NCNTs) showed higher OER activities in an alkaline solution than the individual metal hybrids (Ni@NCNTs and Co@NCNTs), highlighting a synergy between the Ni and Co components. NiCo@NCNTs pyrolyzed at 800 °C displayed an overpotential of ∼41 mV at a current density of 10 mA cm-2 and were more stable than IrO2 during 1000-cycle accelerated durability testing at a scan rate of 100 mV s-1.

  2. Influence of Chemical Composition on Rupture Properties at 1200 Degrees F. of Forged Chromium-Cobalt-Nickel-Iron Base Alloys in Solution-Treated and Aged Condition

    NASA Technical Reports Server (NTRS)

    Reynolds, E E; Freeman, J W; White, A E

    1951-01-01

    The influence of systematic variations of chemical composition on rupture properties at 1200 degrees F. was determined for 62 modifications of a basic alloy containing 20 percent chromium, 20 percent nickel, 20 percent cobalt, 3 percent molybdenum, 2 percent tungsten, 1 percent columbium, 0.15 percent carbon, 1.7 percent manganese, 0.5 percent silicon, 0.12 percent nitrogen and the balance iron. These modifications included individual variations of each of 10 elements present and simultaneous variations of molybdenum, tungsten, and columbium. Laboratory induction furnace heats were hot-forged to round bar stock, solution-treated at 2200 degrees F., and aged at 1400 degrees F. The melting and fabrication conditions were carefully controlled in order to minimize all variable effects on properties except chemical composition. Information is presented which indicates that melting and hot-working conditions play an important role in high-temperature properties of alloys of the type investigated.

  3. High strength cast aluminum alloy development

    NASA Astrophysics Data System (ADS)

    Druschitz, Edward A.

    The goal of this research was to understand how chemistry and processing affect the resulting microstructure and mechanical properties of high strength cast aluminum alloys. Two alloy systems were investigated including the Al-Cu-Ag and the Al-Zn-Mg-Cu systems. Processing variables included solidification under pressure (SUP) and heat treatment. This research determined the range in properties that can be achieved in BAC 100(TM) (Al-Cu micro-alloyed with Ag, Mn, Zr, and V) and generated sufficient property data for design purposes. Tensile, stress corrosion cracking, and fatigue testing were performed. CuAl2 and Al-Cu-Fe-Mn intermetallics were identified as the ductility limiting flaws. A solution treatment of 75 hours or longer was needed to dissolve most of the intermetallic CuAl 2. The Al-Cu-Fe-Mn intermetallic was unaffected by heat treatment. These results indicate that faster cooling rates, a reduction in copper concentration and a reduction in iron concentration might increase the ductility of the alloy by decreasing the size and amount of the intermetallics that form during solidification. Six experimental Al-Zn-Mg-Cu series alloys were produced. Zinc concentrations of 8 and 12wt% and Zn/Mg ratios of 1.5 to 5.5 were tested. Copper was held constant at 0.9%. Heat treating of the alloys was optimized for maximum hardness. Al-Zn-Mg-Cu samples were solution treated at 441°C (826°F) for 4 hours before ramping to 460°C (860°F) for 75 hours and then aged at 120°C (248°F) for 75 hours. X-ray diffraction showed that the age hardening precipitates in most of these alloys was the T phase (Mg32Zn 31.9Al17.1). Tensile testing of the alloys showed that the best mechanical properties were obtained in the lowest alloy condition. Chilled Al-8.2Zn-1.4Mg-0.9Cu solidified under pressure resulted in an alloy with a yield strength of 468MPa (68ksi), tensile strength of 525MPa (76ksi) and an elongation of 9%.

  4. Microstructures and mechanical properties of compositionally complex Co-free FeNiMnCr18 FCC solid solution alloy

    DOE PAGES

    Wu, Z.; Bei, H.

    2015-07-01

    Recently, a structurally-simple but compositionally-complex FeNiCoMnCr high entropy alloy was found to have excellent mechanical properties (e.g., high strength and ductility). To understand the potential of using high entropy alloys as structural materials for advanced nuclear reactor and power plants, it is necessary to have a thorough understanding of their structural stability and mechanical properties degradation under neutron irradiation. Furthermore, this requires us to develop a similar model alloy without Co because material with Co will make post-neutron-irradiation testing difficult due to the production of the 60Co radioisotope. In order to achieve this goal, a FCC-structured single-phase alloy with amore » composition of FeNiMnCr18 was successfully developed. This near-equiatomic FeNiMnCr18 alloy has good malleability and its microstructure can be controlled by thermomechanical processing. By rolling and annealing, the as-cast elongated-grained-microstructure is replaced by homogeneous equiaxed grains. The mechanical properties (e.g., strength and ductility) of the FeNiMnCr18 alloy are comparable to those of the equiatomic FeNiCoMnCr high entropy alloy. Both strength and ductility increase with decreasing deformation temperature, with the largest difference occurring between 293 and 77 K. Extensive twin-bands which are bundles of numerous individual twins are observed when it is tensile-fractured at 77 K. No twin bands are detected by EBSD for materials deformed at 293 K and higher. Ultimately the unusual temperature-dependencies of UTS and uniform elongation could be caused by the development of the dense twin substructure, twin-dislocation interactions and the interactions between primary and secondary twinning systems which result in a microstructure refinement and hence cause enhanced strain hardening and postponed necking.« less

  5. Elevated temperature fracture of RS/PM aluminum alloy 8009

    NASA Technical Reports Server (NTRS)

    Porr, William C., Jr.; Yang, Leng; Gangloff, Richard P.

    1991-01-01

    The fracture behavior of advanced powder metallurgy Al-Fe-V-Si alloy 8009 (previously called FVS0812) is being characterized under monotonic loads, as a function of temperature. Particular attention is focused on contributions to the fracture mechanism from the fine grained dispersoid strengthened microstructure, dissolved solute from rapid solidification, and the moist air environment. Time-dependent crack growth is characterized in advanced aluminum alloys at elevated temperatures with the fracture mechanics approach, and cracking mechanisms are examined with a metallurgical approach. Specific tasks were to obtain standard load crack growth experimental information from a refined testing system; to correlate crack growth kinetics with the j-integral and time dependent C(sub t)(t); and to investigate the intermediate temperature embrittlement of 8009 alloy in order to understand crack growth mechanisms.

  6. Effect of traveling magnetic field on solute distribution and dendritic growth in unidirectionally solidifying Sn-50 wt%Pb alloy: An in situ observation

    NASA Astrophysics Data System (ADS)

    Cao, Fei; Yang, Fenfen; Kang, Huijun; Zou, Cunlei; Xiao, Tiqiao; Huang, Wanxia; Wang, Tongmin

    2016-09-01

    Synchrotron X-ray radiography was used to in situ study the solute distribution and the dendritic growth during the bottom-up solidification of Sn-50 wt%Pb alloy under a traveling magnetic field (TMF) for the first time. The buoyance driven evolution and motion of the plumes containing Sn-rich melt are directly observed in the solidification front before the application of TMF. A forced melt flow from left to right is induced with the application of TMF, which results in the redistribution of the solute concentration (facilitate the solute transportation and reduce the local fluctuations considerably) and the change of the dendrite morphologies (promote/suppress the growth of the secondary arms, remelting and fragmentation of dendrites). Meanwhile, the concentration variations of Sn around the solidification front are quantitatively analyzed through the extraction of gray level from sequenced X-ray images.

  7. Vacancy trapping by solute atoms during quenching in Cu-based dilute alloys studied by positron annihilation spectroscopy

    NASA Astrophysics Data System (ADS)

    Yabuuchi, A.; Yamamoto, Y.; Ohira, J.; Sugita, K.; Mizuno, M.; Araki, H.; Shirai, Y.

    2009-11-01

    Frozen-in vacancies and the recovery have been investigated in some Cu-based dilute alloys by using positron annihilation lifetime spectroscopy. Cu-0.5at%Sb, Cu-0.5at%Sn and Cu-0.5at%In dilute bulk alloys were quenched to ice water from 1223 K. A pure-Cu specimen was also quenched from the same temperature. As a result, no frozen-in vacancies have been detected in as-quenched pure-Cu specimen. On the other hand, as-quenched Cu-0.5at%Sb alloy contained frozen-in thermal equilibrium vacancies with concentration of 3 × 10-5. Furthermore, these frozen-in vacancies in Cu-0.5at%Sb alloy were stable until 473 K, and began to migrate at 523 K. Finally, the Cu-Sb alloy were recovered to the fully annealed state at 823 K. This thermal stability clearly implies some interaction exists between a vacancy and Sb atom and due to the interaction, thermal equilibrium vacancies are trapped by Sb atoms during quenching.

  8. MRI-compatible Nb-60Ta-2Zr alloy for vascular stents: Electrochemical corrosion behavior in simulated plasma solution.

    PubMed

    Li, Hui-Zhe; Zhao, Xu; Xu, Jian

    2015-11-01

    Using revised simulated body fluid (r-SBF), the electrochemical corrosion behavior of an Nb-60Ta-2Zr alloy for MRI compatible vascular stents was characterized in vitro. As indicated by XPS analysis, the surface passive oxide film of approximately 1.3nm thickness was identified as a mixture of Nb2O5, Ta2O5 and ZrO2 after immersion in the r-SBF. The Nb-60Ta-2Zr alloy manifests a low corrosion rate and high polarization resistance similar to pure Nb and Ta, as shown by the potentiodynamic polarization curves and EIS. Unlike 316L stainless steel and the L605 Co-Cr alloy, no localized corrosion has been detected. Semiconducting property of passive film on the Nb-60Ta-2Zr alloy was identified as the n-type, with growth mechanism of high-field controlled growth. The excellent corrosion resistance in simulated human blood enviroment renders the Nb-60Ta-2Zr alloy promising as stent candidate material. Copyright © 2015 Elsevier B.V. All rights reserved.

  9. Solute transport in formations of very low permeability: profiles of stable isotope and dissolved noble gas contents of pore water in the Opalinus Clay, Mont Terri, Switzerland

    NASA Astrophysics Data System (ADS)

    Rübel, André P.; Sonntag, Christian; Lippmann, Johanna; Pearson, F. J.; Gautschi, Andreas

    2002-04-01

    Pore water profiles of water, stable isotope, and dissolved noble gas content have been determined across the Opalinus Clay and adjacent formations at the rock laboratory at Mont Terri. We have found enhanced helium contents (up to [ 4He] = 1 × 10 -4 cubic centimeters at standard pressure and temperature per gram of pore water) and argon isotope ratios ( 40Ar/ 36Ar ratios up to 334) due to accumulation of 4He and 40Ar produced in situ. The helium profile was found to be in steady state with respect to in situ production and diffusive loss into the adjacent limestones where groundwater circulates. From this profile a representative mean value of the apparent diffusion coefficient for helium in the pore water of the whole formation was derived for the first time to be D a = 3.5 × 10 -11 m 2 · s -1, which is more than two orders of magnitude lower than the diffusion coefficient D 0 in free water. The stable isotope profile, however, indicates a component of fossil marine pore water, which has not yet been replaced by molecular diffusion of meteoric water from the adjacent limestone and shale formations over the past 10 million years.

  10. Tracing ground-water evolution in a limestone aquifer using Sr isotopes: Effects of multiple sources of dissolved ions and mineral-solution reactions

    NASA Astrophysics Data System (ADS)

    Banner, Jay L.; Musgrove, Marylynn; Capo, R. C.

    1994-08-01

    Uplifted Pleistocene coral-reef terraces on Barbados, West Indies, constitute an aquifer that is built on low-permeability Tertiary pelagic rocks that overlie the Barbados accretionary prism. The downdip segments of the aquifer are composed of younger reef limestones that contain more aragonite and have higher 87Sr/86Sr and Sr/Ca ratios than the updip parts of the aquifer. Ground waters and host limestones display similar stratigraphic trends in 87Sr/86Sr and Sr/Ca. The ground waters have lower 87Sr/86Sr values, however, indicating that they acquire a significant fraction of their dissolved Sr through interaction with components of Tertiary rocks, which compose the underlying aquitard and parts of overlying soils. Geochemical modeling results indicate that ground-water evolution is controlled by (1) variations in the age and composition of the aquifer and aquitard rocks and (2) the relative roles of calcite dissolution, calcite recrystallization, and the transformation of aragonite to calcite. Sr isotopes can provide unique information for tracing ground-water evolution, which requires consideration of the multiple components and processes that make up even relatively simple limestone aquifer systems.

  11. Dissolved gas - the hidden saboteur

    SciTech Connect

    Magorien, V.G.

    1993-12-31

    Almost all hydraulic power components, to properly perform their tasks, rely on one basic, physical property, i.e., the incompressibility of the working fluid. Unfortunately, a frequently overlooked fluid property which frustrates this requirement is its ability to absorb, i.e., dissolve, store and give off gas. The gas is, most often but not always, air. This property is a complex one because it is a function not only of the fluid`s chemical make-up but temperature, pressure, exposed area, depth and time. In its relationshiop to aircraft landing-gear, where energy is absorbed hydraulically, this multi-faceted fluid property can be detrimental in two ways: dynamically, i.e., loss of energy absorption ability and statically, i.e., improper aircraft attitude on the ground. The pupose of this paper is to bring an awareness to this property by presenting: (1) examples of these manifestations with some empirical and practical solutions to them, (2) illustrations of this normally `hidden saboteur` at work, (3) Henry`s Dissolved Gas Law, (4) room-temperature, saturated values of dissolved gas for a number of different working fluids, (5) a description of the instrument used to obtain them, (6) some `missing elements` of the Dissolved Gas Law pertaining to absoption, (7) how static and dynamic conditions effect gas absorption and (8) some recommended solutions to prevent becoming a victim of this `hidden saboteur`

  12. Effect of TiO 2 addition on crack propagation of alloy 600 and its penetration into crevices in caustic solution

    NASA Astrophysics Data System (ADS)

    Kim, Uh Chul; Kim, Kyung Mo; Kang, Jung Soo; Lee, Eun Hee; Kim, Hong Pyo

    2002-04-01

    A number of tubes of nuclear steam generators have experienced stress corrosion cracking in environments thought to be caustic. Wedged CT specimens of Alloy 600 were used to measure crack propagation rates with and without TiO 2 in a 10% NaOH solution at 315 °C. The crack propagation rate was reduced by 1/2 with 2 g/l TiO 2 addition. Polarization curves showed an extensive decrease of the anodic peak current and passive current with TiO 2 addition in a 10% NaOH solution at 315 °C. The TiO 2 penetration into crevices was investigated using Alloy 600 specimens having different gap sizes in a 1% NaOH solution at 315 °C with TiO 2 addition. The Ti concentration of the specimens was analyzed in crevices by Auger electron spectroscopy after a 3-day exposure. The Ti concentration was 42% or more in crevices wider than 0.2 mm and 20% in the narrowest crevice with 0.05 mm.

  13. Effect of atomic size on undercoolability of binary solid solution alloy liquids with Zr, Ti, and Hf using electrostatic levitation

    NASA Astrophysics Data System (ADS)

    Jeon, S.; Kang, D.-H.; Lee, Y. H.; Lee, S.; Lee, G. W.

    2016-11-01

    We investigate the relationship between the excess volume and undercoolability of Zr-Ti and Zr-Hf alloy liquids by using electrostatic levitation. Unlike in the case of Zr-Hf alloy liquids in which sizes of the constituent atoms are matched, a remarkable increase of undercoolability and negative excess volumes are observed in Zr-Ti alloy liquids as a function of their compositional ratios. In this work, size mismatch entropies for the liquids were obtained by calculating their hard sphere diameters, number densities, and packing fractions. We also show that the size mismatch entropy, which arises from the differences in atomic sizes of the constituent elements, plays an important role in determining the stabilities of metallic liquids.

  14. The Electrochemical Behavior of Mo-Ta Alloy in Phosphoric Acid Solution for TFT-LCD Application.

    PubMed

    Lee, Sang-Hyuk; Kim, Byoung O; Seo, Jong Hyun

    2015-10-01

    Molybdenum-tantalum alloy thin film is a suitable material for the higher corrosion resistance and low resistivity for gate and data metal lines. In this study, Mo-Ta alloy thin films were prepared by using a DC magnetron co-sputtering system on a glass substrate. An abrupt increase in the etching rates of low Mo-Ta alloys was observed. From the observed impedance analysis, the defect densities in the MoTa oxide films increased from 5.4 x 10(21) (cm(-3)) to 8.02 x 10(21) (cm(-3)) up to the 6 at% of tantalum level; and above the 6 at% of tantalum level, the defect densities decreased. This electrochemical behavior is explained by the mechanical instability of the MoTa oxide film.

  15. Effect of atomic size on undercoolability of binary solid solution alloy liquids with Zr, Ti, and Hf using electrostatic levitation.

    PubMed

    Jeon, S; Kang, D-H; Lee, Y H; Lee, S; Lee, G W

    2016-11-07

    We investigate the relationship between the excess volume and undercoolability of Zr-Ti and Zr-Hf alloy liquids by using electrostatic levitation. Unlike in the case of Zr-Hf alloy liquids in which sizes of the constituent atoms are matched, a remarkable increase of undercoolability and negative excess volumes are observed in Zr-Ti alloy liquids as a function of their compositional ratios. In this work, size mismatch entropies for the liquids were obtained by calculating their hard sphere diameters, number densities, and packing fractions. We also show that the size mismatch entropy, which arises from the differences in atomic sizes of the constituent elements, plays an important role in determining the stabilities of metallic liquids.

  16. A Practical Anodic and Cathodic Curve Intersection Model to Understand Multiple Corrosion Potentials of Fe-Based Glassy Alloys in OH- Contained Solutions

    PubMed Central

    Li, Y. J.; Wang, Y. G.; An, B.; Xu, H.; Liu, Y.; Zhang, L. C.; Ma, H. Y.; Wang, W. M.

    2016-01-01

    A practical anodic and cathodic curve intersection model, which consisted of an apparent anodic curve and an imaginary cathodic line, was proposed to explain multiple corrosion potentials occurred in potentiodynamic polarization curves of Fe-based glassy alloys in alkaline solution. The apparent anodic curve was selected from the measured anodic curves. The imaginary cathodic line was obtained by linearly fitting the differences of anodic curves and can be moved evenly or rotated to predict the number and value of corrosion potentials. PMID:26771194

  17. Anti-corrosion film formed on HAl77-2 copper alloy surface by aliphatic polyamine in 3 wt.% NaCl solution

    NASA Astrophysics Data System (ADS)

    Yu, Yinzhe; Yang, Dong; Zhang, Daquan; Wang, Yizhen; Gao, Lixin

    2017-01-01

    The corrosion inhibition of a polyamine compound, N-(4-amino-2, 3-dimethylbutyl)-2, 3-dimethylbutane-1, 4-diamine (ADDD), was investigated for HAl77-2 copper alloy in 3 wt.% NaCl solution. Electrochemical measurements, scanning electron microscopy (SEM), atomic force microscope (AFM) and Fourier transform infrared spectroscopy (FT-IR) techniques were employed for this research. The results show that ADDD strongly suppresses the corrosion of HAl77-2 alloy. The inhibition efficiency of ADDD is 98.6% at 0.5 mM, which is better than benzotriazole (BTAH) at the same concentration. Polarization curves indicate that ADDD is an anodic type inhibitor. Surface analysis suggests that a protective film is formed via the interaction of ADDD and copper. FT-IR reveals that the inhibition mechanism of ADDD is dominated by chemisorption onto the copper alloy surface to form an inhibition film. Furthermore, quantum chemical calculation and molecular dynamics (MD) simulations methods show that ADDD adsorbs on HAl77-2 surface via amino group in its molecule.

  18. Effects of Cr, Zr, V, Mn, Fe, and Co to the hydride properties of Laves phase-related body-centered-cubic solid solution alloys

    NASA Astrophysics Data System (ADS)

    Young, K.; Ouchi, T.; Nei, J.; Meng, T.

    2015-05-01

    Chemical composition modifications of a Laves phase-related BCC solid solution base alloy, Ti15.6Zr2.1V44Cr11.2Mn6.9Fe2.7Co1.4Ni15.7Al0.3, were investigated in order to study the function of each constituent element on the structural, gaseous phase and electrochemical hydrogen storage properties of these alloys. In general, removal of Fe and decrease in V-content in exchange for higher Ni-content were found to improve both the electrochemical capacity and high-rate dischargeability, which are related to the decrease in C14-content and increase in TiNi-content. However, total elimination of the C14 phase by removal of Zr resulted in a reduced discharge capacity, a prolonged activation period, and a less catalytic surface for electrochemical reaction. Besides the BCC and C14 phases, the TiNi phase was also found in every alloy in this study, contributing positively to the bulk diffusion of hydrogen while hindering the surface electrochemical reaction.

  19. Ground-fire effects on the composition of dissolved and total organic matter in forest floor and soil solutions from Scots pine forests in Germany: new insights from solid state 13C NMR analysis

    NASA Astrophysics Data System (ADS)

    Näthe, Kerstin; Michalzik, Beate; Levia, Delphis; Steffens, Markus

    2016-04-01

    Fires represent an ecosystem disturbance and are recognized to seriously pertubate the nutrient budgets of forested ecosystems. While the effects of fires on chemical, biological, and physical soil properties have been intensively studied, especially in Mediterranean areas and North America, few investigations examined the effects of fire-induced alterations in the water-bound fluxes and the chemical composition of dissolved and particulate organic carbon and nitrogen (DOC, POC, DN, PN). The exclusion of the particulate organic matter fraction (0.45 μm < POM < 500 μm) potentially results in misleading inferences and budgeting gaps when studying the effects of fires on nutrient and energy fluxes. To our best knowledge, this is the first known study to present fire-induced changes on the composition of dissolved and total organic matter (DOM, TOM) in forest floor (FF) and soil solutions (A, B horizon) from Scots pine forests in Germany. In relation to control sites, we test the effects of low-severity fires on: (1) the composition of DOM and TOM in forest floor and soil solutions; and (2) the translocated amount of particulate in relation to DOC and DN into the subsoil. The project aims to uncover the mechanisms of water-bound organic matter transport along an ecosystem profile and its compositional changes following a fire disturbance. Forest floor and soil solutions were fortnightly sampled from March to December 2014 on fire-manipulated and control plots in a Scots pine forest in Central Germany. Shortly after the experimental duff fire in April 2014 pooled solutions samples were taken for solid-state 13C NMR spectroscopy to characterize DOM (filtered solution < 0.8μm pore size) and TOM in unfiltered solutions. Independent from fire manipulation, the composition of TOM was generally less aromatic (aromaticity index [%] according to Hatcher et al., 1981) with values between 18 (FF) - 25% (B horizon) than the DOM fraction with 23 (FF) - 27% (B horizon). For DOM

  20. Precipitation phase transformation in nanocrystalline Fe-Mo alloys.

    PubMed

    Sarkar, Subhajit; Bansal, Chandrahaas

    2004-01-01

    Precipitation phase transformation was studied in nanocrystalline Fe-rich Fe-Mo alloys with the use of X-ray diffraction and Mössbauer spectroscopy. Alloys up to 5 at% Mo in Fe were synthesized by mechanical alloying and formed in alpha phase bcc solid solutions with average grain sizes in the range of 10-13 nm. The precipitation transformation (alpha-->alpha + lambda) was found to proceed via a Mo clustering that was correlated with the size of the nanograins. This was understood in terms of the Gibbs Thomson effect with a concept of negative surface energy contribution to the Gibbs free energy of mixing in a nanocrystalline alloy with positive internal energy of mixing. This contribution increased the stability of the solid solution for nanosized grains, and the Mo precipitation started once the grains grew beyond a critical size. We argue that the Mo precipitation takes place in the grain boundary regions, and the Mo-rich lambda phase also precipitates directly in the grain boundary regions, in contrast to the microcrystalline alloys, where the Mo clusters formed within the grains and were first dissolved in the Fe matrix before the lambda phase was formed.

  1. Effects of dissolved Ca2+, Mg2+, and Na+ ions on the supramolecular aggregation of natural organic matter in aqueous solutions

    NASA Astrophysics Data System (ADS)

    Ahn, W.; Kalinichev, A. G.; Clark, M. M.

    2008-12-01

    The complexation of natural organic matter (NOM) with metal ions, minerals and organic species in soil and water allows NOM to form water-soluble and water-insoluble aggregates of widely differing chemical and biological stabilities. Metal-NOM interaction induces strong correlations between the concentration of natural organic matter and the speciation, solubility and toxicity of many metals in the environment. In water purification and desalination, NOM is also implicated in fouling of nanofiltration and reverse osmosis membranes, either as the primary foulant or as a conditioning layer for microbial attachment ("biofouling"). In this work we investigated the effects of various metal ions on NOM aggregation in aqueous solutions, by a combination of dynamic light scattering (DLS), small angle neutron scattering (SANS) and large-scale molecular dynamics (MD) computer simulations. This allows a detailed molecular-scale statistical analysis of the size and the structural topology of metal-NOM aggregates. The DLS measurements show that Ca2+ ions present in a Suwannee River NOM (SRNOM) solution lead to the formation of a wide range of supramolecular structures with sizes between 100 and 1,000 nm. In contrast, Mg2+ and Na+ do not affect the aggregation of SRNOM as strongly. SANS data are inconclusive but indicate the presence of quite large (>50 nm) fractal particles formed presumably through a cluster-cluster aggregation. MD simulations confirm these observations and show that NOM can aggregate in aqueous solutions by two different mechanisms. On the one hand, NOM molecules can spontaneously aggregate by hydrogen bonding between their functional groups when only Na+ and Mg2+ are present as background cations. This promotes the formation of uniformly shaped NOM clusters. On the other hand, if Ca2+ ions are present in solution, they can more strongly bind two different NOM molecules by co-complexing the carboxylate groups, thus promoting the formation of longer linear and

  2. Corrosion behavior of Pd-Cu and Pd-Co alloys in synthetic saliva.

    PubMed

    Goehlich, V; Marek, M

    1990-04-01

    Pd-based alloys are major alternatives to gold-based alloys for PFM applications. In electrolytes simulating oral fluids, these alloys exhibit electrode behavior similar to passivity of active metals, i.e., a potential region of almost constant current density up to a critical potential, above which the current increases. The objective of this study was to correlate the electrode behavior with the results of solution analyses and changes in the surface composition of the alloys. Binary alloys Pd-15 wt% Cu and Pd-19 wt% Co, as well as the pure components, were examined. Corrosion potentials vs. time, potentiodynamic anodic polarization curves, polarization resistances vs. time, and potentiostatic anodic charges were measured with synthetic saliva used as the electrolyte. The concentrations of Pd, Cu, and Co in the solution after various exposures were determined by atomic absorption. The surfaces of the alloys were examined by x-ray photoelectron spectroscopy before and after the exposures. The results show that selective dissolution of the less-noble components occurred on the surfaces of both alloys for all the exposures, leaving the surfaces highly enriched in Pd. This enrichment contributed to the potential changes and the passive-type behavior. Copper dissolved more than cobalt at longer exposures and higher potentials, in spite of its higher nobility. Dissolution of cobalt seemed to be limited by the formation of a surface film, which may be related to the transition character of this element.

  3. Erosion patterns on dissolving blocks

    NASA Astrophysics Data System (ADS)

    Courrech du Pont, Sylvain; Cohen, Caroline; Derr, Julien; Berhanu, Michael

    2016-04-01

    Patterns in nature are shaped under water flows and wind action, and the understanding of their morphodynamics goes through the identification of the physical mechanisms at play. When a dissoluble body is exposed to a water flow, typical patterns with scallop-like shapes may appear [1,2]. These shapes are observed on the walls of underground rivers or icebergs. We experimentally study the erosion of dissolving bodies made of salt, caramel or ice into water solutions without external flow. The dissolving mixture, which is created at the solid/liquid interface, undergoes a buoyancy-driven instability comparable to a Rayleigh-Bénard instability so that the dissolving front destabilizes into filaments. This mechanism yields to spatial variations of solute concentration and to differential dissolution of the dissolving block. We first observe longitudinal stripes with a well defined wavelength, which evolve towards chevrons and scallops that interact and move again the dissolving current. Thanks to a careful analysis of the competing physical mechanisms, we propose scaling laws, which account for the characteristic lengths and times of the early regime in experiments. The long-term evolution of patterns is understood qualitatively. A close related mechanism has been proposed to explain structures observed on the basal boundary of ice cover on brakish lakes [3] and we suggest that our experiments are analogous and explain the scallop-like patterns on iceberg walls. [1] P. Meakin and B. Jamtveit, Geological pattern formation by growth and dissolution in aqueous systems, Proc. R. Soc. A 466, 659-694 (2010). [2] P.N. Blumberg and R.L. Curl, Experimental and theoretical studies of dissolution roughness, J. Fluid Mech. 65, 735-751 (1974). [3] L. Solari and G. Parker, Morphodynamic modelling of the basal boundary of ice cover on brakish lakes, J.G.R. 118, 1432-1442 (2013).

  4. Tracer Film Growth Study of the Corrosion of Magnesium Alloys AZ31B and ZE10A in 0.01% NaCl Solution

    DOE PAGES

    Brady, M. P.; Fayek, M.; Leonard, D. N.; ...

    2017-05-25

    We conducted a sequential isotopic tracer study of corrosion film growth for Mg-3Al-1Zn-0.25Mn (AZ31B) and Mg-1.2Zn-0.25Zr-<0.5Nd (ZE10A) by 4 h immersion in H218O or D216O, followed by a 20 h immersion in a 0.01 wt% NaCl H218O or D216O solution. Sputter depth profiles were obtained for 16O, 18O, H, and D using secondary ion mass spectrometry (SIMS). When compared to the previous tracer study for these alloys in salt-free water, the addition of 0.01 wt% NaCl resulted in a transition from oxygen inward-dominated film growth to a component of mixed inward/outward film growth for both alloys. The hydrogen tracer behaviormore » remained inward growing for AZ31B, and short-circuit, inward growing for ZE10A, in both pure water and in 0.01 wt% NaCl solution, with extensive penetration of D beyond the film and into the underlying alloy also observed for ZE10A. Our analysis of the films by X-ray photoelectron spectroscopy (XPS) and cross-section scanning transmission electron microscopy (STEM) indicated intermixed Mg(OH)2 and MgO, with the relative fraction of Mg(OH)2 peaking near the center of the film. These findings suggest a decoupled film growth mechanism, with initial formation of oxide followed by NaCl-accelerated conversion to hydroxide, likely by both solid-state and dissolution-precipitation processes.« less

  5. A study of effects of acid activated saw dust on the removal of different dissolved tannery dyes (acid dye) from aqueous solutions.

    PubMed

    Dhar, N R; Khoda, A K M B; Khan, A H; Bala, P; Karim, M F

    2005-04-01

    The effectiveness of acid activated sawdust in absorbing D-Brown EGP and Lurazol Brown PM dyes from aqueous solutions was studied as a function of agitation time and initial dye concentration. The experimental data were fitted to Langmuir and Freundlich isotherm and found that adsorption process follows both the isotherms. The values of Langmuir and Freundlich constants indicate favorable and beneficial adsorption. Saw dust is an excellent low cost adsorbent of colored organic anions and may have significant potential as a color removal from tannery wastewater.

  6. Effect of Sn4+ Additives on the Microstructure and Corrosion Resistance of Anodic Coating Formed on AZ31 Magnesium Alloy in Alkaline Solution

    NASA Astrophysics Data System (ADS)

    Salman, S. A.; Kuroda, K.; Saito, N.; Okido, M.

    Magnesium is the lightest structural metal with high specific strength and good mechanical properties. However, poor corrosion resistance limits its widespread use in many applications. Magnesium is usually treated with Chromate conversion coatings. However, due to changing environmental regulations and pollution prevention requirements, a significant push exists to find new, alternative for poisonous Cr6+. Therefore, we aim to improve corrosion resistance of anodic coatings on AZ31 alloys using low cost non-chromate electrolyte. Anodizing was carried out in alkaline solutions with tin additives. The effect of tin additives on the coating film was characterized by SEM and XRD. The corrosion resistance was evaluated using anodic and cathodic polarizations and electrochemical impedance spectroscopy (EIS). Corrosion resistance property was improved with tin additives and the best anti-corrosion property was obtained with addition of 0.03 M Na2SnO3.3H2O to anodizing solution.

  7. Microstructural evolution and magnetic properties of ultrafine solute-atom particles formed in a Cu75-Ni20-Fe5 alloy on isothermal annealing

    NASA Astrophysics Data System (ADS)

    Kim, Jun-Seop; Takeda, Mahoto; Bae, Dong-Sik

    2016-12-01

    Microstructural features strongly affect magnetism in nano-granular magnetic materials. In the present work we have investigated the relationship between the magnetic properties and the self-organized microstructure formed in a Cu75-Ni20-Fe5 alloy comprising ferromagnetic elements and copper atoms. High resolution transmission electron microscopy (HRTEM) observations showed that on isothermal annealing at 873 K, nano-scale solute (Fe,Ni)-rich clusters initially formed with a random distribution in the Cu-rich matrix. Superconducting quantum interference device (SQUID) measurements revealed that these ultrafine solute clusters exhibited super-spinglass and superparamagnetic states. On further isothermal annealing the precipitates evolved to cubic or rectangular ferromagnetic particles and aligned along the <100> directions of the copper-rich matrix. Electron energy-band calculations based on the first-principle Korringa-Kohn-Rostocker (KKR) method were also implemented to investigate both the electronic structure and the magnetic properties of the alloy. Inputting compositions obtained experimentally by scanning transmission electron microscopy-electron dispersive X-ray spectroscopy (STEM-EDS) analysis, the KKR calculation confirmed that ferromagnetic precipitates (of moment 1.07μB per atom) formed after annealing for 2 × 104 min. Magneto-thermogravimetric (MTG) analysis determined with high sensitivity the Curie temperatures and magnetic susceptibility above room temperature of samples containing nano-scale ferromagnetic particles.

  8. Corrosion Behavior of Thermally Sprayed NiCrBSi Coating on 16MnR Low-Alloy Steel in KOH Solution

    NASA Astrophysics Data System (ADS)

    Zeng, Q.; Sun, J.; Emori, W.; Jiang, S. L.

    2016-05-01

    NiCrBSi coatings were selected as protective material and air plasma-sprayed on 16MnR low-alloy steel substrates. Corrosion behavior of 16MnR substrates and NiCrBSi coatings in KOH solution were evaluated by polarization resistance ( R p), potentiodynamic polarization curves, electrochemical impedance spectroscopy, and immersion corrosion tests. Electrolytes were solutions with different KOH concentrations. NiCrBSi coating showed superior corrosion resistance in KOH solution compared with the 16MnR. Corrosion current density of 16MnR substrate was 1.7-13.0 times that of NiCrBSi coating in the given concentration of KOH solution. By contrast, R p of NiCrBSi coating was 1.2-8.0 times that of the substrate, indicating that the corrosion rate of NiCrBSi coating was much lower than that of 16MnR substrate. Capacitance and total impedance value of NiCrBSi coating were much higher than those of 16MnR substrate in the same condition. This result indicates that corrosion resistance of NiCrBSi coating was better than that of 16MnR substrate, in accordance with polarization results. NiCrBSi coatings provided good protection for 16MnR substrate in KOH solution. Corrosion products were mainly Ni/Fe/Cr oxides.

  9. XPS study of bioactive graded layer in Ti-In-Nb-Ta alloy prepared by alkali and heat treatments.

    PubMed

    Lee, Baek-Hee; Kim, Young Do; Lee, Kyu Hwan

    2003-06-01

    Ti and Ti-based alloys have been widely used for the biomedical applications due to their superiorities of biocompatibility, mechanical properties and corrosion resistance. However, there has been the limiting factor for these metals to show the low affinity to the living bone. Most of commercially used Ti alloys have harmful alloying elements such as Al, V, etc. The purposes of this study are design of new Ti alloy having the good mechanical properties and corrosion resistivity without harmful alloying elements and to improve the bone-bonding ability between Ti-based alloy and living bone through the chemically activated process (alkali treatment) and thermally activated one (heat treatment). Mechanical properties of the Ti-In-Nb-Ta alloy were observed by tensile test (Instron model 8511). Corrosion potential and corrosion rate were investigated using a Potentiostate machine (EG&G, Princeton Applied Model 273, Boston, USA) with saline solution (9% NaCl) without dissolved oxygen at 37 degrees C. After alkali and heat treatments, the effects of the pre-treatments on the bonding property were evaluated by in vitro test. In this study, the surface changing behavior, which is apatite formation, of newly designed Ti-In-Nb-Ta alloy without harmful alloying elements was investigated through analyzing its surface by using X-ray photoelectron spectroscopy after surface activation treatments (alkali and heat treatments) and after subsequent soaking in the simulated body fluid.

  10. Hydrogen trapping by solute atoms in Nb-Mo(3 at. %) alloys as observed by the channeling method

    NASA Astrophysics Data System (ADS)

    Yagi, Eiichi; Nakamura, Shiho; Kano, Fumihisa; Kobayashi, Takane; Watanabe, Kenji; Fukai, Yuh; Matsumoto, Takehiko

    1989-01-01

    In order to elucidate the mechanism of the enhancement of the terminal solubility for hydrogen (TSH) in Nb by alloying with undersized Mo atoms, the state of hydrogen was studied by the channeling method using a nuclear reaction 1H(11B, α)αα in Nb-Mo(3 at. %) alloys. At room temperature H atoms are located at sites displaced from tetrahedral (T) sites by about 0.6 Å towards the nearest-neighbor lattice points, while at 373 K they are at T sites. These results give direct evidence for trapping of hydrogen by Mo atoms and strongly support the trapping model for the enhancement of the TSH in the low-concentration region of Mo atoms.

  11. Hydrogen trapping by solute atoms in Nb--Mo(3 at. %) alloys as observed by the channeling method

    SciTech Connect

    Yagi, E.; Nakamura, S.; Kano, F.; Kobayashi, T.; Watanabe, K.; Fukai, Y.; Matsumoto, T.

    1989-01-01

    In order to elucidate the mechanism of the enhancement of the terminal solubility for hydrogen (TSH) in Nb by alloying with undersized Mo atoms, the state of hydrogen was studied by the channeling method using a nuclear reaction /sup 1/H(/sup 11/B, ..cap alpha..)..cap alpha cap alpha.. in Nb--Mo(3 at. %) alloys. At room temperature H atoms are located at sites displaced from tetrahedral (T) sites by about 0.6 A towards the nearest-neighbor lattice points, while at 373 K they are at T sites. These results give direct evidence for trapping of hydrogen by Mo atoms and strongly support the trapping model for the enhancement of the TSH in the low-concentration region of Mo atoms.

  12. Thermogravimetric Thin Aqueous Film Corrosion Studies of Alloy 22; Calcium Chloride Solutions at 150C and Atmospheric Pressure

    SciTech Connect

    Hailey, P; Gdoowski, G

    2002-11-12

    The extent of reaction of alloy-22 with limited amounts of aqueous calcium chloride (CaCl{sub 2}) was investigated. Alloy-22 is a highly corrosion-resistant nickel-chromium-molybdenum-tungsten alloy. Specimens were polished to a mirror finish prior to aerosol salt deposition. An aqueous film was formed by deliquescence of deposited CaCl{sub 2} at 150 C and 22.5% relative humidity (RH). The reactant gas was a continuous flow of purified humidified laboratory air. The reaction progress as a function of time was continuously measured in-situ by a micro-balance. An initial weight gain due to deliquescence of the CaCl{sub 2} was observed. A steady weight loss was observed over the next 72 hours, after which no further weight change was observed. During this weight loss, white precipitates formed and the specimen's surface became visibly dry. The precipitate crystals were identified as Ca(OH){sub 2} by post-test Raman spectroscopy; however, energy dispersive X-ray spectroscopy indicated that there was a significant amount of chlorine contained in them.

  13. Postweld solution annealing effects on the ductility of Ni-Co-Cr-base alloy gas tungsten arc welds

    SciTech Connect

    Lim, C.S.; Baek, K.K.

    1996-12-01

    The welding characteristics of a commercial wrought alloy with a nominal composition of Ni-29Co-28Cr-2.75Si were investigated. Gas tungsten arc weldments with filler metal matching the chemistry of the alloy were found to have limited room-temperature ductility in the as-welded condition. Since welding is the main fabrication method of this alloy, the welding and postweld heat treatment (PWHT) characteristics were examined to provide guidelines for fabrication in the field. Metallographic evaluation revealed that the weld metal was characterized by the distribution of a continuous eutectic phase consisting primarily of (Si, Ti){sub x}Ni{sub y}. The continuous eutectic phase in the as-welded deposit, which caused poor ductility of the welds, was successfully reduced or removed with proper PWHT. The PWHT is necessary if cold forming of a weldment is required after welding or if adequate joint ductility is a design requirement. The recommended PWHT temperature is 1,050 C.

  14. Sequential Determination of Free Acidity and Plutonium Concentration in the Dissolver Solution of Fast-Breeder Reactor Spent Fuels in a Single Aliquot.

    PubMed

    Dhamodharan, K; Pius, Anitha

    2016-01-01

    A simple potentiometric method for determining the free acidity without complexation in the presence of hydrolysable metal ions and sequentially determining the plutonium concentration by a direct spectrophotometric method using a single aliquot was developed. Interference from the major fission products, which are susceptible to hydrolysis at lower acidities, had been investigated in the free acidity measurement. This method is applicable for determining the free acidity over a wide range of nitric acid concentrations as well as the plutonium concentration in the irradiated fuel solution prior to solvent extraction. Since no complexing agent is introduced during the measurement of the free acidity, the purification step is eliminated during the plutonium estimation, and the resultant analytical waste is free from corrosive chemicals and any complexing agent. Hence, uranium and plutonium can be easily recovered from analytical waste by the conventional solvent extraction method. The error involved in determining the free acidity and plutonium is within ±1% and thus this method is superior to the complexation method for routine analysis of plant samples and is also amenable for remote analysis.

  15. Extraction Equilibrium of Mn2+, Ca2+, and Mg2+ from Chloride Solutions by Di(2-ethylhexyl)phosphoric Acid Dissolved in Kerosene

    NASA Astrophysics Data System (ADS)

    Zhang, Chuanfu; Cao, Wenxin; Zhan, Jing; Ding, Fenghua; Hwang, Jiann-Yang

    2015-05-01

    The presence of calcium and magnesium affects the purity of the final product MnCl2 in hydrometallurgical treatment processes. The solvent extraction method can be used to separate Ca2+ and Mg2+ from Mn2+ solutions containing impurity ions such as Ca2+ and Mg2+. This article aims to investigate the single-stage extraction equilibrium of Ca2+, Mg2+, and Mn2+ in chloride medium using di(2-ethylhexyl)phosphoric acid in kerosene (O:A = 1:1). The results show that the pH0.5 values are 1.11, 1.56, and 2.18 for Ca2+, Mn2+, and Mg2+, respectively. The mechanism of extraction and stoichiometries of metal-containing extracted species were illustrated based on a slope analysis. The composition of the extracted species in the organic phase is proposed to be MnR2·R2H2, CaR2·R2H2, and MgR2·(R2H2)2, respectively.

  16. METHOD FOR DISSOLVING LANTHANUM FLUORIDE CARRIER FOR PLUTONIUM

    DOEpatents

    Koshland, D.E. Jr.; Willard, J.E.

    1961-08-01

    A method is described for dissolving lanthanum fluoride precipitates which is applicable to lanthanum fluoride carrier precipitation processes for recovery of plutonium values from aqueous solutions. The lanthanum fluoride precipitate is contacted with an aqueous acidic solution containing dissolved zirconium in the tetravalent oxidation state. The presence of the zirconium increases the lanthanum fluoride dissolved and makes any tetravalent plutonium present more readily oxidizable to the hexavalent state. (AEC)

  17. Method for dissolving plutonium oxide with HI and separating plutonium

    DOEpatents

    Vondra, Benedict L.; Tallent, Othar K.; Mailen, James C.

    1979-01-01

    PuO.sub.2 -containing solids, particularly residues from incomplete HNO.sub.3 dissolution of irradiated nuclear fuels, are dissolved in aqueous HI. The resulting solution is evaporated to dryness and the solids are dissolved in HNO.sub.3 for further chemical reprocessing. Alternatively, the HI solution containing dissolved Pu values, can be contacted with a cation exchange resin causing the Pu values to load the resin. The Pu values are selectively eluted from the resin with more concentrated HI.

  18. Stress Corrosion Cracking Behavior of Multipass TIG-Welded AA2219 Aluminum Alloy in 3.5 wt pct NaCl Solution

    NASA Astrophysics Data System (ADS)

    Venugopal, A.; Sreekumar, K.; Raja, V. S.

    2012-09-01

    The stress corrosion cracking (SCC) behavior of the AA2219 aluminum alloy in the single-pass (SP) and multipass (MP) welded conditions was examined and compared with that of the base metal (BM) in 3.5 wt pct NaCl solution using a slow-strain-rate technique (SSRT). The reduction in ductility was used as a parameter to evaluate the SCC susceptibility of both the BM and welded joints. The results showed that the ductility ratio ( ɛ NaCl/( ɛ air) was 0.97 and 0.96, respectively, for the BM and MP welded joint, and the same was marginally reduced to 0.9 for the SP welded joint. The fractographic examination of the failed samples revealed a typical ductile cracking morphology for all the base and welded joints, indicating the good environmental cracking resistance of this alloy under all welded conditions. To understand the decrease in the ductility of the SP welded joint, preexposure SSRT followed by microstructural observations were made, which showed that the decrease in ductility ratio of the SP welded joint was caused by the electrochemical pitting that assisted the nucleation of cracks in the form of corrosion induced mechanical cracking rather than true SCC failure of the alloy. The microstructural examination and polarization tests demonstrated a clear grain boundary (GB) sensitization of the PMZ, resulting in severe galvanic corrosion of the SP weld joint, which initiated the necessary conditions for the localized corrosion and cracking along the PMZ. The absence of PMZ and a refined fusion zone (FZ) structure because of the lesser heat input and postweld heating effect improved the galvanic corrosion resistance of the MP welded joint greatly, and thus, failure occurred along the FZ.

  19. Alloy Semiconductor Crystal Growth Under Microgravity

    SciTech Connect

    Hayakawa, Yasuhiro; Arivanandhan, Mukannan; Rajesh, Govindasamy; Tanaka, Akira; Ozawa, Tetsuo; Okano, Yasunori; Sankaranarayanan, Krishnasamy; Inatomi, Yuko

    2010-12-01

    Microgravity studies on the dissolution and crystallization of In{sub x}Ga{sub 1-x}Sb have been done using a sandwich combination of InSb and GaSb as the starting material using the Chinese recoverable satellite. The same type of experiment was performed under 1G gravity condition for comparison. From these experiments and the numerical simulation, it is found that the shape of the solid/liquid interface and composition profile in the solution was found to be significantly affected by gravity. GaSb seed was dissolved faster than GaSb feed even though the GaSb feed temperature was higher than that of GaSb seed temperature. These results clearly indicate that solute transport due to gravity affects dissolution and growth processes of alloy semiconductor bulk crystals.

  20. Metastable alloy nanoparticles, metal-oxide nanocrescents and nanoshells generated by laser ablation in liquid solution: influence of the chemical environment on structure and composition.

    PubMed

    Scaramuzza, Stefano; Agnoli, Stefano; Amendola, Vincenzo

    2015-11-14

    Alloy nanoparticles are characterized by the combination of multiple interesting properties, which are attractive for technological and scientific purposes. A frontier topic of this field is nanoalloys with compositions not thermodynamically allowed at ordinary temperature and pressure (i.e. metastable), because they require out-of-equilibrium synthetic approaches. Recently, laser ablation synthesis in solution (LASiS) was successfully applied for the realization of metastable nanoalloys because of the fast kinetics of nanoparticle formation. However, the role played by the chemical environment on the final composition and structure of laser generated nanoalloys still has to be fully elucidated. Here, we investigated the influence of different synthetic conditions on the LASiS of metastable nanoalloys composed of Au and Fe, such as the use of water instead of ethanol, the bubbling of inert gases and the addition of a few vol% of H2O2 and H2O. The two elements showed different reactivity when LASiS was performed in water instead of ethanol, while minor effects were observed from bubbling pure gases such as N2, Ar and CO2 in the liquid solution. Moreover, the plasmonic response and the structure of the nanoalloys were sensibly modified by adding H2O2 to water. We also found that nanoparticle production is dramatically influenced just by adding 0.2% of H2O in ethanol. These results suggest that the formation of a cavitation bubble with long lifetime and large size during LASiS is useful for the preservation of the metastable alloy composition, whereas an oxidative environment hampers the formation of metastable alloy nanoparticles. Overall, by acting on the type of solvent and solutes, we were able to switch from a traditional synthetic approach for the composition of Au-Fe nanoalloys to one using a reactive environment, which gives unconventional structures such as metal@iron-oxide nanoshells and nanocrescents of oxide supported on metal nanospheres. These results