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Search indexed NASA NTRS and DOE OSTI research on propulsion, heat transfer, battery materials and energy systems. Follow report and document links to the original sources.

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At least 19 records
All sourcesNASA NTRSDOE OSTI
DOE OSTI2017

Galvanic cell for processing of used nuclear fuel

A galvanic cell and methods of using the galvanic cell is described for the recovery of uranium from used nuclear fuel according to an electrofluorination process. The galvanic cell requires no input energy and can utilize relatively benign gaseous fluorinating agents. Uranium can be recovered from used nuclear fuel in the form of gaseous uranium compound such as uranium hexafluoride, which can then be converted to metallic uranium or UO.sub.2 and processed according to known methodology to form a useful product, e.g., fuel pellets for use in a commercial energy production system.

11 NUCLEAR FUEL CYCLE AND FUEL MATERIALS↗
NASA NTRS2003

The Feasibility of Using a Galvanic Cell Array for Corrosion Detection and Solution Monitoring

An initial investigation into the response of the individual galvanic couples was conducted using potentiodynamic polarization measurements of solutions under conditions of varying corrosivity. It is hypothesized that the differing electrodes may provide a means to further investigate the corrosive nature of the analyte through genetic algorithms and pattern recognition techniques. The robust design of the electrochemical sensor makes its utilization in space exploration particularly attractive. Since the electrodes are fired on a ceramic substrate at 900 C, they may be one of the most rugged sensors available for the anticipated usage.

Kolody, Mark↗
DOE OSTI2016

Electrochemical fluorination for processing of used nuclear fuel

A galvanic cell and methods of using the galvanic cell is described for the recovery of uranium from used nuclear fuel according to an electrofluorination process. The galvanic cell requires no input energy and can utilize relatively benign gaseous fluorinating agents. Uranium can be recovered from used nuclear fuel in the form of gaseous uranium compound such as uranium hexafluoride, which can then be converted to metallic uranium or UO.sub.2 and processed according to known methodology to form a useful product, e.g., fuel pellets for use in a commercial energy production system.

11 NUCLEAR FUEL CYCLE AND FUEL MATERIALS↗
DOE OSTI2014

Atomic-scale decoration for improving the pitting corrosion resistance of austenitic stainless steels

Stainless steels are susceptible to the localized pitting corrosion that leads to a huge loss to our society. Studies in the past decades confirmed that the pitting events generally originate from the local dissolution in MnS inclusions which are more or less ubiquitous in stainless steels. Although a recent study indicated that endogenous MnCr 2 O 4 nano-octahedra within the MnS medium give rise to local nano-galvanic cells which are responsible for the preferential dissolution of MnS, effective solutions of restraining the cells from viewpoint of electrochemistry are being tantalizingly searched. Here we report such a galvanic corrosion can be greatly resisted via bathing the steels in Cu 2+ -containing solutions. This chemical bath generates Cu 2–δ S layers on the surfaces of MnS inclusions, invalidating the nano-galvanic cells. Our study provides a low-cost approach via an atomic scale decoration to improve the pitting corrosion resistance of stainless steels in a volume-treated manner.

36 MATERIALS SCIENCE↗
DOE OSTI2018

Corrosion behaviors of friction welded dissimilar aluminum alloys

Highlights: • Corrosion properties of friction welded dissimilar aluminum alloys seem to be governed by the anode part in the weld. • Intense corrosion near the interface has the limited region due to insufficient ionic transport. • Self-formation of a micro-galvanic cell is a main reason for the inferior corrosion performance. - Abstract: Corrosion behaviors of the friction welded dissimilar aluminum alloys were investigated to understand how galvanic effect plays a role in altering corrosion properties of the dissimilar weld. From the fact that the weld had the similar OCP value to that of AA2017, it can be inferred that the corrosion characteristics of the weld is under the control of the AA2017 part in the weld and as a result, only the AA2017 part in the weld had experienced severe corrosion, leaving AA6063 under cathodic protection. Intense corrosion occurring near the interface implies that the area near the interface is placed under the effect of galvanic corrosion and there was the effective distance where the galvanic effect exerts an impact due to the increase in the resistance of the electrolyte with the distance from the interface. The disappearance of Warburg diffusion plot in Nyquist plots for the weld seemed to be the breakdown of the passivation layer related to the formation of the micro-galvanic cell, which in turn presented the shrinkage in the capacitance response, indicating that charge reactions in the form of corrosion occurred.

36 MATERIALS SCIENCE↗
NASA NTRS1990

A simple demonstration of corrosion cells

The objective is to reinforce and enhance the understanding of galvanic cells, anode cathode reactions and polarization phenomena. Complete instructions are given for laboratory demonstration to be performed by students.

Guichelaar, Philip J.↗
NASA NTRS1973

Electromotive force measurements on cells involving beta-alumina solid electrolyte

Open circuit emf measurements have been made to demonstrate that a two-phase, polycrystalline mixture of beta- alumina and alpha-alumina could be used as a solid electrolyte in galvanic cells with reversible electrodes fixing oxygen or aluminum chemical potentials. These measurements indicate that such a two phase solid electrolyte can be used to monitor oxygen chemical potentials as low as that corresponding to Al, Al2O3 coexistence. The activity of Na2O in beta-alumina in coexistence with alpha-alumina was also determined by emf measurements.

Choudhury, N.↗
NASA NTRS1973

Electromotive force measurements on cells involving beta-alumina solid electrolyte

Open-circuit emf measurements have been made to demonstrate that a two-phase, polycrystalline mixture of beta-alumina and alpha-alumina could be used as a solid electrolyte in galvanic cells with reversible electrodes fixing oxygen or aluminum chemical potentials. These measurements indicate that such a two-phase solid electrolyte may be used to monitor oxygen chemical potentials as low as that corresponding to Al and Al2O3 coexistence (potentials of about 10 to the minus 47th power atm at 1000 K). The activity of Na2O in beta-alumina in coexistence with alpha-alumina was also determined by emf measurements.

Choudhury, N. S.↗
NASA NTRS1978

Some studies on a solid-state sulfur probe for coal gasification systems

As a part of a program for the development of a sulfur probe for monitoring the sulfur potential in coal gasification reactors, an investigation was conducted regarding the efficiency of the solid electrolyte cell Ar+H2+H2S/CaS+CaF2+(Pt)//CaF2//Pt)+CaF2+CaS/H2S+H2+Ar. A demonstration is provided of the theory, design, and operation of a solid-state sulfur probe based on CaF2 electrolyte. It was found that the cell responds to changes in sulfur potential in a manner predicted by the Nernst equation. The response time of the cell at 1225 K, after a small change in temperature or gas composition, was 2.5 Hr, while at a lower temperature of 990 K the response time was approximately 9 hr. The cell emf was insensitive to a moderate increase in the flow rate of the test gas and/or the reference gas. The exact factors affecting the slow response time of galvanic cells based on a CaF2 electrolyte have not yet been determined. The rate-limiting steps may be either the kinetics of electrode reactions or the rate of transport through the electrolyte.

Jacob, K. T.↗
NASA NTRS1999

Electrochemical Measurement of Atmospheric Corrosion

Corrosion of Shuttle thruster components in atmospheres containing high concentrations of nitrogen tetroxide (NTO) and water is an important issue in ground operations of bipropellant systems in humid locations. Measurements of the corrosivities of NTO-containing atmospheres and the responses of different materials to these atmospheres have been accomplished using an electrochemical sensor. The sensor is composed of alternating aluminum/titanium strips separated by thin insulating layers. Under high humidity conditions a thin film of water covers the surface of the sensor. Added NTO vapor reacts with the water film to form a conductive medium and establishes a galvanic cell. The current from this cell can be integrated with respect to time and related to the corrosion activity. The surface layer formed from humid air/NTO reacts in the same way as an aqueous solution of nitric acid. Nitric acid is generally considered an important agent in NTO corrosion situations. The aluminum/titanium sensor is unresponsive to dry air, responds slightly to humid air (> 75% RH), and responds strongly to the combination of humid air and NTO. The sensor response is a power function (n = 2) of the NTO concentration. The sensor does not respond to NTO in dry air. The response of other materials in this type of sensor is related to position of the material in a galvanic series in aqueous nitric acid. The concept and operation of this electrochemical corrosion measurement is being applied to other corrosive atmospheric contaminants such as hydrogen chloride, hydrogen fluoride, sulfur dioxide, and acidic aerosols.

DeArmond, Anna H.↗
NASA NTRS2001

Thermodynamic Activity Measurements with Knudsen Cell Mass Spectrometry

Coupling the Knudsen effusion method with mass spectrometry has proven to be one of the most useful experimental techniques for studying the equilibrium between condensed phases and complex vapors. The Knudsen effusion method involves placing a condensed sample in a Knudsen cell, a small "enclosure", that is uniformly heated and held until equilibrium is attained between the condensed and vapor phases. The vapor is continuously sampled by effusion through a small orifice in the cell. A molecular beam is formed from the effusing vapor and directed into a mass spectrometer for identification and pressure measurement of the species in the vapor phase. Knudsen cell mass spectrometry (KCMS) has been used for nearly fifty years now and continues to be a leading technique for obtaining thermodynamic data. Indeed, much of the well-established vapor specie data in the JANAF tables has been obtained from this technique. This is due to the extreme versatility of the technique. All classes of materials can be studied and all constituents of the vapor phase can be measured over a wide range of pressures (approximately 10(exp -4) to 10(exp -11) bar) and temperatures (500-2800 K). The ability to selectively measure different vapor species makes KCMS a very powerful tool for the measurement of component activities in metallic and ceramic solutions. Today several groups are applying KCMS to measure thermodynamic functions in multicomponent metallic and ceramic systems. Thermodynamic functions, especially component activities, are extremely important in the development of CALPHAD (Calculation of Phase Diagrams) type thermodynamic descriptions. These descriptions, in turn, are useful for modeling materials processing and predicting reactions such as oxide formation and fiber/matrix interactions. The leading experimental methods for measuring activities are the Galvanic cell or electro-motive force (EMF) technique and the KCMS technique. Each has specific advantages, depending on material and conditions. The EMF technique is suitable for lower temperature measurements, provided a suitable cell can be constructed. KCMS is useful for higher temperature measurements in a system with volatile components. In this paper, we briefly review the KCMS technique and identify the major experimental issues that must be addressed for precise measurements. These issues include temperature measurements, cell material and cell design and absolute pressure calibration. The resolution of these issues are discussed together with some recent examples of measured thermodynamic data.

Copland, Evan H.↗
DOE OSTI2016

Effect of aqueous‐based cathode slurry pH and immersion time on corrosion of aluminum current collector in lithium‐ion batteries

Corrosion of aluminum can occur during the manufacturing of lithium‐ion batteries when using aqueous‐based cathode slurries. In exposure tests, the alkaline pH value of aqueous‐based cathode slurries and immersing time were revealed as the principle factors that control the corrosion of aluminum during the cathode manufacturing process. The nickel manganese cobalt oxide active material used in the slurry does not have a direct impact on corrosion of the aluminum current collector. The initiation and evolution of localized corrosion on aluminum are closely related to the formation of galvanic cells between aluminum matrix and intermetallic particles. X‐ray photoelectron spectroscopy results confirmed that the pH of cathode slurry was the only factor that alters aluminum surface composition, during which the oxide passive film was gradually degraded into hydroxide. Electrochemical characterizations showed that aluminum electrodes gave remarkably different response to the different pH of test solutions. The time‐pH‐variant electrochemical response was ascribed to the change of passive film and electric double layer properties.

Li, S. Y.↗
DOE OSTI2019

Corrosion Investigation of Zinc–Aluminum Alloy (ZA-27) Matrix Reinforced with In Situ Synthesized Titanium Carbide Particle Composites

ZA-27 alloy matrix composites comprised of different volume fractions of TiC particles as reinforcement phase were synthesized by in situ technique. Microstructural, hardness and electrochemical analysis were performed on these samples along with the base ZA-27 alloy to assess any beneficial effect of making the composites over the base alloy. It was observed that hardness increases in composites as compared to the base alloy. However, hardness of the composite reduces on increasing the reinforcement percentage. Corrosion behavior was investigated by using Tafel and EIS plots in 3.5 wt.% NaCl solution at room temperature for all the samples. The results showed increase in corrosion resistance for composites than that of base alloy. However, ZA27 + 5%TiC composite showed better results as compared to that of ZA27 + 10%TiC composite. The decreased property of ZA27 + 10%TiC composite is because of the agglomeration of particles and also by the formation of galvanic cell.

36 MATERIALS SCIENCE↗
DOE OSTI2019

Effect of Carbon Nanotube Concentration on the Corrosion Behavior of Electroless Ni-B-CNT Coating

In this study, Ni-B-CNT composite was deposited on AISI 4140 steel using different concentrations of CNTs ranging from 0.2 to 1 gr/lit in an electroless bath. The phase analysis and surface morphology of the samples were characterized using x-ray diffraction and FESEM. The corrosion behavior of the coated samples was investigated in a 3.5 wt.% NaCl solution through potentiodynamic polarization, EIS, and electrochemical noise (EN) analyses. The corroded surface of the samples was further analyzed via FESEM observation after 10 days of immersion in corrosive medium. It was found that although adding 0.2 gr/lit CNT in electroless solution improves corrosion resistance, increasing CNT concentration from 0.2 up to 1 gr/lit increases the corrosion rate. The FESEM observations and EN results imply that the formation of micro-galvanic cells in samples with high concentration of CNTs leads to nucleation and growth of the pits. The results revealed that no passive layer was formed on the surface of the Ni-B sample, and the corrosion occurred through ionic diffusion into the cracks and crevices. The results of potentiodynamic test show that adding CNTs into electroless bath facilitates the formation of passive layer. However, results of EN test imply that increasing CNT concentration causes repetitive breakdown and recovery of passive film.

36 MATERIALS SCIENCE↗