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Relevant bibliographies by topics / SALT-METAL

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Academic literature on the topic 'SALT-METAL'

Author: Grafiati

Published: 11 September 2023

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Journal articles on the topic "SALT-METAL"

1

Christie, Robert M., and Jennifer L. Mackay. "Metal salt azo pigments." Coloration Technology 124, no. 3 (June 2008): 133–44. http://dx.doi.org/10.1111/j.1478-4408.2008.00133.x.

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Silvestrelli, Pier Luigi, Ali Alavi, Michele Parrinello, and Daan Frenkel. "Nonmetal-metal transition in metal–molten-salt solutions." Physical Review B 53, no. 19 (May 15, 1996): 12750–60. http://dx.doi.org/10.1103/physrevb.53.12750.

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JUSSIPBEKOV, U. Zh, R. M. CHERNYAKOVA, A. A. АGATAYEVA, N. N. KOZHABEKOVA, R. А. KAIYNBAYEVA, and G. Sh SULTANBAYEVA. "SORPTION OF HEAVY METAL CATIONS FROM A WATER-SALT SYSTEMBY NATURAL MONTMORILLONITE." Chemical Journal of Kazakhstan 73, no. 1 (March 14, 2021): 204–12. http://dx.doi.org/10.51580/2021-1/2710-1185.22.

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The sorption properties of natural montmorillonite from the Tagan deposit with respect to heavy metal cations were researched on the model system "Mn2+–Co2+– Ni2+–V4+–H2O–montmorillonite". The influence of temperature, duration of the process and concentration of solutions, as well as the norm of the sorbent on the degree of sorption of cations is considered. The optimal conditions for the sorption process (25о С, 30 min, Т:Ж = 1,5:100) have been determined, at which the degree of solution purification is up to 86.36% cations of Co2+, 85.59% of Ni2+, 82.64% of Mn2+ and 52.29% of V4+. The nature of the sorption curves is determined by the nature of the sorbed cation. According to the absorption efficiency of natural montmorillonite, ions are arranged in the following order: Ni2+≥ Co2+> Mn2+> V4+. The results of the conducted studies indicate the possibility of effective use of bentonite clays of the Tagan field in the purification of wastewater from heavy metal cations

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Li, Yongjiang, Xiaoyan Ma, Jingyu Ma, Zongwu Zhang, Zhaoqi Niu, and Fang Chen. "Fabrication of Pore-Selective Metal-Nanoparticle-Functionalized Honeycomb Films via the Breath Figure Accompanied by In Situ Reduction." Polymers 13, no. 3 (January 20, 2021): 316. http://dx.doi.org/10.3390/polym13030316.

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Honeycomb films pore-filled with metal (Au, Ag, and Cu) nanoparticles were successfully prepared by combining the breath figure method and an in situ reduction reaction. First, a polyhedral oligomeric silsesquioxane (POSS)-based star-shaped polymer solution containing metal salt was cast under humid conditions for the formation of honeycomb films pore-filled with metal salt through the breath figure method. The morphology of the honeycomb films was mainly affected by the polymer molecular structure and the metal salt. Interestingly, the promoting effect of the metal salt in the breath figure process was also observed. Then, honeycomb films pore-filled with metal nanoparticles were obtained by in situ reduction of the honeycomb films pore-filled with metal salt using NaBH4. Notably, the metal nanoparticles can be selectively functionalized in the pores or on the surface of the honeycomb films by controlling the concentration of the NaBH4. Metal-nanoparticle-functionalized honeycomb films can prospectively be used in catalysis, flexible electrodes, surface-enhanced Raman spectroscopy (SERS), and wettability patterned surfaces.

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Flint, Edward B., and Kenneth S. Suslick. "Sonoluminescence from alkali-metal salt solutions." Journal of Physical Chemistry 95, no. 3 (February 1991): 1484–88. http://dx.doi.org/10.1021/j100156a084.

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Weber, Mirco, David Vorobev, and Wolfgang Viöl. "Microwave Plasma-Enhanced Parylene–Metal Multilayer Design from Metal Salts." Nanomaterials 12, no. 15 (July 24, 2022): 2540. http://dx.doi.org/10.3390/nano12152540.

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In this paper, a new approach for the synthesis of Parylene–metal multilayers was examined. The metal layers were derived from a metal salt solution in methanol and a post-drying plasma reduction treatment. This process was designed as a one-pot synthesis, which needs a very low amount of resources and energy compared with those using electron beam sputtering processes. The Parylene coatings were obtained after reduction plasma treatments with Parylene C. Therefore, a Parylene coating device with an included plasma microwave generator was used to ensure the character of a one-pot synthesis. This process provided ultra-thin metal salt layers in the range of 1–2 nm for layer thickness and 10–30 nm for larger metal salt agglomerates all over the metal salt layer. The Parylene layers were obtained with thicknesses between approx. 4.5 and 4.7 µm from ellipsometric measurements and 5.7–6.3 µm measured by white light reflectometry. Tensile strength analysis showed an orthogonal pulling stress resistance of around 4500 N. A surface roughness of 4–8 nm for the metal layers, as well as 20–29 nm for the Parylene outer layer, were measured. The wettability for non-polar liquids with a contact angle of 30° was better than for polar liquids, such as water, achieving 87° on the Parylene C surfaces.

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Sun, Dezhi, Wenqing Zheng, Xiukui Qu, and Ling Li. "Enthalpies of Dilution formyo-Inositol in Aqueous Alkali Metal Salt and Alkaline Earth Metal Salt Solutions." Journal of Chemical & Engineering Data 52, no. 3 (May 2007): 898–901. http://dx.doi.org/10.1021/je060492g.

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Meyerhoffer, Steven M., and Linda B. McGown. "Fluorescent probe studies of metal salt effects on bile salt aggregation." Journal of the American Chemical Society 113, no. 6 (March 1991): 2146–49. http://dx.doi.org/10.1021/ja00006a036.

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Saito, Hiroki, and Shinji Koyama. "Solid-State Bonding of 5052 Aluminum Alloy/316L Stainless Steel by Using Organic Salt Formation/Decomposition Reaction." Materials Science Forum 879 (November 2016): 2468–72. http://dx.doi.org/10.4028/www.scientific.net/msf.879.2468.

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The effect of metal salt coating process on the bond strength of the bonded interface of 5052 aluminum alloy and 316L stainless steel was investigated by SEM observations of interfacial microstructures and fractured surfaces. Aluminum alloy surfaces were coated by boiling in 5% aqueous solution of NaOH for 5 s and 98% formic acid and 99.7% acetic acid for 20 s and 20 s respectively. Bonding process was performed at bonding temperature of 733 ~ 773 K under a pressure of 20 MPa (bonding time of 900 s). From this study, it is found out that the bonded strength of the joint increased with the rise in bonding temperature with or without metal salt coating process. However, it is understood that with metal salt coating process, high strength joint can be achieved with lesser deformation and lower bonding temperature. From the experimental results, it is found out that metal salt generation processing is effective at removing oxide film and substitution to a metal salt on the aluminum surface.

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Kim, Hyunjin, Ji Eun Song, Carla Silva, and Hye Rim Kim. "Production of conductive bacterial cellulose-polyaniline membranes in the presence of metal salts." Textile Research Journal 90, no. 13-14 (December 16, 2019): 1517–26. http://dx.doi.org/10.1177/0040517519893717.

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This study presents a cost-effective method of enhancing the electrical conductivity and washing durability of bacterial cellulose (BC)-polyaniline (PANI) membrane by the addition of metal salt. In this study, two types of metal salts were tested: copper (II) sulfate and iron (II) sulfate. The optimal condition to produce BC-PANI-metal salt membranes was 0.05% (w/v) of copper (II) sulfate (copper salt). X-ray diffraction analysis showed that the crystallinity of BC-PANI increased after adding copper salt. According to the increased degree of crystallinity, the polymer chain structure of BC-PANI-copper salt (BC-PANI-Cu) was more organized than that of BC-PANI, as confirmed by scanning electron microscopy. In addition, this ordered structure of BC-PANI-Cu indicated enhanced electrical conductivity. Moreover, the addition of copper salt improved the electrical conductivity of BC-PANI to a level about 3.8 times higher than that of BC-PANI produced without metal salt, and it retained about 40% of its original electrical conductivity after three washing cycles. From the results, the addition of copper salt improved both the electrical conductivity and washing durability of the BC-PANI membrane.

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Dissertations / Theses on the topic "SALT-METAL"

1

Brooker, Alan Thomas. "New routes to metal salt complexes." Thesis, University of Cambridge, 1991. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.359761.

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Emmerson, Richard Hugh Christian. "Salt marsh restoration by managed retreat : metal and nutrient fluxes." Thesis, Imperial College London, 1997. http://hdl.handle.net/10044/1/8454.

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Lacombe, Marie. "Synthesis and metal salt binding properties of functionalised macrocyclic ligands." Thesis, University of Nottingham, 2003. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.275160.

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Khandelwal, Amit Harikant. "Lithium, sodium and lanthanide metal inorganic and organic salt complexes." Thesis, University of Cambridge, 1994. https://www.repository.cam.ac.uk/handle/1810/272664.

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Alkhamis, Mohammad, and Mohammad Alkhamis. "Stability of Metal in Molten Chloride Salt at 800˚C." Thesis, The University of Arizona, 2016. http://hdl.handle.net/10150/622893.

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The stability of Haynes 230 and Hastelloy C-276 nickel alloys exposed to high temperature molten salt with trace contaminants (i.e., water and oxygen) is found to be acceptable for using these metals to house anaerobic MgCl2-KCl and NaCl-KCl-ZnCl2 molten salts at 800oC. The corrosion rate determined by gravimetric tests range from -98 µm/year to 20. 13 µm/year at 800˚C. The corrosion rate is estimated to be 16.14 µm/year for Haynes 230 and 10.03 µm/year for Hastelloy C-276 based on the weight loss and surface area of the coupons when the coupons of Haynes 230 and Hastelloy C-276 alloys are immersed in molten MgCl2-KCl salt in sealed quartz containers and left in an oven at a temperature of 800˚C up to 16 days. The corrosion rate is estimated to be -20.46 µm/year for Haynes 230 and -7.36 µm/year for Hastelloy C-276 based on the weight loss and surface area of the coupons when the alloys are immersed in molten NaCl-KCl-ZnCl2 salt in sealed quartz containers and left in an oven at 800˚C up to 56 days. The corrosion rate of the alloys are well below the DOE requirement of 50 µm/year for the alloys in molten chloride salts to be considered acceptably stable. Ultimate tensile strength (UTS) after immersion of Haynes 230 and Hastelloy C-276 in molten salt ranged from 634 MPa to 860 MPa. The UTS of Haynes 230 is estimated to be 642 MPa after exposure to NaCl-KCl-ZnCl2 for 4 weeks at 800˚c and 841 MPa after exposure to MgCl2-KCl for 4 weeks at 800˚c compared to an untreated sample which achieved a UTS of 851 MPa. Likewise, the UTS of Hastelloy C-276 is estimated to be 692 MPa after exposure to NaCl-KCl-ZnCl2 for 4 weeks at 800˚c and 842 MPa after exposure to MgCl2-KCl for 4 weeks at 800˚c compared to an untreated sample which achieved a UTS of 830 MPa. Molten chloride salts, such as NaCl-KCl-ZnCl2 and KCl-MgCl2, are pretreated by heating and bubbling dry Argon gas in the salt in order to remove oxygen and water and thereby reduce the corrosion of metal containers of molten salt. Monitoring the relative humidity and percent oxygen of the exhaust gas during the sparging of dry Argon at 240 sccm into 150 g of molten chloride salt at 500˚C for NaCl-KCl-ZnCl2 and 700˚C for KCl-MgCl2 allows an estimation time to reach a low level of oxygen and water in the salt and to estimate the amount of oxygen and water removed. Results show water is more difficult to remove than oxygen from the salt. Ten minutes of sparging with dry argon brings oxygen content of exhuast gas to<0.1% O2. Approximately fifty minutes of sparging leaves the exhaust gas only containing<0.7% RH. The total moles of oxygen removed from the salts are estimated to be 0.0043 moles for molten NaCl-KCl-ZnCl2 and 0.0076 moles for KCl-MgCl2. The total moles of water removed from the NaCl-KCl-ZnCl2 salt is estimated to be 0.016108379 moles and 0.002321214 moles from molten KCl-MgCl2.

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Fatollahi-Fard, Farzin. "Production of Titanium Metal by an Electrochemical Molten Salt Process." Research Showcase @ CMU, 2017. http://repository.cmu.edu/dissertations/893.

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Titanium production is a long and complicated process. What we often consider to be the standard method of primary titanium production (the Kroll process), involves many complex steps both before and after to make a useful product from titanium ore. Thus new methods of titanium production, especially electrochemical processes, which can utilize less-processed feedstocks have the potential to be both cheaper and less energy intensive than current titanium production processes. This project is investigating the use of lower-grade titanium ores with the electrochemical MER process for making titanium via a molten salt process. The experimental work carried out has investigated making the MER process feedstock (titanium oxycarbide) with natural titanium ores|such as rutile and ilmenite|and new ways of using the MER electrochemical reactor to \upgrade" titanium ores or the titanium oxycarbide feedstock. It is feasible to use the existing MER electrochemical reactor to both purify the titanium oxycarbide feedstock and produce titanium metal.

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7

Saeed-Akbari, Semiramis [Verfasser]. "Minimizing Salt and Metal Losses in Mg-Recycling through Salt Optimization and Black Dross Distillation / Semiramis Saeed-Akbari." Aachen : Shaker, 2011. http://d-nb.info/1071529412/34.

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8

Meyer, Joseph Freeman. "Recovery boiler superheater corrosion - solubility of metal oxides in molten salt." Thesis, Georgia Institute of Technology, 2013. http://hdl.handle.net/1853/47742.

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The recovery boiler in a pulp and paper mill plays a dual role of recovering pulping chemicals and generating steam for either chemical processes or producing electricity. The efficiency of producing steam in the recovery boiler is limited by the first melting temperature of ash deposits that accumulate on the superheater tubes. Above the first melting temperature, the molten salt reacts with the protective oxide film that develops and dissolves it. The most protective oxide is determined by evaluating how little it dissolves and how its solubility changes in the molten salt. Solubility tests were done on several protective oxides in a known salt composition from a recovery boiler that burns hardwood derived fuel. ICP-OES was used to measure concentration of dissolved metal in the exposure tests while EDS and XRD were used to verify chemical compositions in exposure tests. NiO was found to be the least soluble oxide while Cr₂O₃ and Al₂O₃ had similar solubility with Fe₂O₃ being less soluble than Cr₂O₃ but more soluble than NiO. Exposure tests with pure metals and selected alloys indicated that even though Fe₂O₃ has little solubility, it is not a protective oxide and causes severe corrosion in stainless steels. The change in performance of iron based alloys was due to the development of a negative solubility gradient for Fe₂O₃ where Fe₂O₃ precipitated out of solution and created a continuous leaching of oxide. Manganese was found to be beneficial in stainless steels but its role is still unknown. Nickel based alloys were found to be least corroded due to nickel's low solubility and because it did not form a negative solubility gradient.

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9

Tomlinson, Simon Michael. "Computer simulation studies of rock-salt structured binary transition metal oxides." Thesis, University College London (University of London), 1987. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.264941.

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10

Spatocco, Brian Leonard. "Investigation of molten salt electrolytes for low-temperature liquid metal batteries." Thesis, Massachusetts Institute of Technology, 2015. http://hdl.handle.net/1721.1/101461.

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Thesis: Ph. D., Massachusetts Institute of Technology, Department of Materials Science and Engineering, 2015.
This electronic version was submitted by the student author. The certified thesis is available in the Institute Archives and Special Collections.
Cataloged from student-submitted PDF version of thesis.
Includes bibliographical references (pages 202-211).
This thesis proposes to advance our ability to solve the challenge of grid-scale storage by better positioning the liquid metal battery (LMB) to deliver energy at low levelized costs. It will do this by rigorously developing an understanding of the cost structure for LMBs via a process-based cost model, identifying key cost levers to serve as filters for system down-selection, and executing a targeted experimental program with the goal of both advancing the field as well as improving the LMB's final cost metric. Specifically, cost modelling results show that temperature is a key variable in LMB system cost as it has a multiplicative impact upon the final $/kWh cost metric of the device. Lower temperatures can reduce the total cost via simultaneous simplifications in device sealing, packaging, and wiring. In spite of this promise, the principal challenge in reducing LMB operating temperatures (>400°C) lies in identifying high conductivity, low-temperature electrolytes that are thermally, chemically, and electrochemically stable with pure molten metals. For this reason, a research program investigating a promising low-temperature binary molten salt system, NaOH-NaI, is undertaken. Thermodynamic studies confirm a low eutectic melting temperature (219°C) and, together with the identification of two new binary compounds via x-ray diffraction, it is now possible to construct a complete phase diagram. These phase equilibrium data have then been used to optimize Gibbs free energy functions for the intermediate compounds and a two-sublattice sub-regular solution framework to create a thermodynamically self-consistent model of the full binary phase space. Further, a detailed electrochemical study has identified the electrochemical window (>2.4 V) and related redox reactions and found greatly improved stability of the pure sodium electrode against the electrolyte. Results from electrochemical studies have been compared to predictions from the solution model and strong agreement supports the physicality of the model. Finally, a Na[/]NaOH-NaI[/]Pb-Bi proof-of-concept cell has achieved over 100 cycles and displayed leakage currents below 0.40 mA/cm℗ø. These results highlight an exciting new class of low-melting molten salt electrolytes and point to a future Na-based low-temperature system that could achieve costs that are 10-15% less than those of existing lithium-based LMBs.
by Brian Leonard Spatocco.
Ph. D.

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Books on the topic "SALT-METAL"

1

Saeed-Akbari, Semiramis. Minimizing salt and metal losses in Mg-recycling through salt optimization and black dross distillation. Aachen: Shaker, 2011.

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2

Murphy, J. E. Production of lead metal by molten-salt electrolysis with energy-efficient electrodes. Washington, DC: Bureau of Mines, U.S. Dept. of the Interior, 1990.

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Murphy, J. E. Production of lead metal by molten-salt electrolysis with energy-efficient electrodes. Washington, DC: Bureau of Mines, U.S. Dept. of the Interior, 1990.

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4

International, ASM, ed. Guide to pickling and descaling, and molten salt bath cleaning. Materials Park, OH: ASM International, 1996.

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5

Kunetz, James Michael. The chemical behavior of heavy metal salt solutions within porous sol-gel silica. 1995.

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Phillips, Barbara M. Marine Bioassay Project: 10th Report: Metal, Ammonia, Sediment And Artificial Salt Toxicity Evaluations On Marine Test Organisms. Diane Pub Co, 2000.

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Guidance on Selecting a Strategy for Assessing the Ecological risk of Organometallic and Organic Metal Salt Substances based on their Environmental Fate. OECD, 2017. http://dx.doi.org/10.1787/9789264274785-en.

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Hinton, David A. The Medieval Workshop. Edited by Christopher Gerrard and Alejandra Gutiérrez. Oxford University Press, 2018. http://dx.doi.org/10.1093/oxfordhb/9780198744719.013.21.

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Archaeological evidence of medieval production is mostly in the form of residues rather than of workshops, although pits and hearths have been excavated. Apart from bone and antler, few organic products survive, unlike metal objects. This chapter considers the evidence for agricultural processing and production, textiles, metal-working, carcass products such as tanning, shoe-making, and bone-working, as well as stone, mineral (e.g. salt), and the more familiar clay products of pottery and tile production. Most recent developments have been in analyses, distribution studies, and considerations of the financial values and personal meanings of medieval objects. Most workshops were small scale and often temporary; only the cloth industry had the capacity to raise the capital required for substantial investment.

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Challenges Related to the Use of Liquid Metal and Molten Salt Coolants in Advanced Reactors: Report of the Collaborative Project COOL of the International Project on Innovative Nuclear Reactors and Fuel Cycles. International Atomic Energy Agency, 2013.

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Book chapters on the topic "SALT-METAL"

1

Warren, W. W. "Metal-Metal Salt Solutions." In Molten Salt Chemistry, 237–57. Dordrecht: Springer Netherlands, 1987. http://dx.doi.org/10.1007/978-94-009-3863-2_11.

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Zingaro, R. A. "Using Metal Salt Derivatives." In Inorganic Reactions and Methods, 132. Hoboken, NJ, USA: John Wiley & Sons, Inc., 2007. http://dx.doi.org/10.1002/9780470145197.ch102.

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Bonaplata, E., C. D. Smith, and J. E. McGrath. "Metal Salt—Polymer Composites." In ACS Symposium Series, 227–37. Washington, DC: American Chemical Society, 1995. http://dx.doi.org/10.1021/bk-1995-0603.ch015.

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Bothe, Hermann, Marjana Regvar, and Katarzyna Turnau. "Arbuscular Mycorrhiza, Heavy Metal,and Salt Tolerance." In Soil Biology, 87–111. Berlin, Heidelberg: Springer Berlin Heidelberg, 2009. http://dx.doi.org/10.1007/978-3-642-02436-8_5.

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Purakayastha, T. J., Asit Mandal, and Savita Kumari. "Phytoremediation of Metal- and Salt-Affected Soils." In Bioremediation of Salt Affected Soils: An Indian Perspective, 211–31. Cham: Springer International Publishing, 2017. http://dx.doi.org/10.1007/978-3-319-48257-6_11.

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Warren, William W. "Electronic Properties of Metal/Molten Salt Solutions." In Molten Salts: From Fundamentals to Applications, 23–46. Dordrecht: Springer Netherlands, 2002. http://dx.doi.org/10.1007/978-94-010-0458-9_2.

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Taxil, Pierre. "Refractory Metal Production by Molten Salt Electrolysis." In Encyclopedia of Applied Electrochemistry, 1801–6. New York, NY: Springer New York, 2014. http://dx.doi.org/10.1007/978-1-4419-6996-5_456.

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Boyce, G., J. R. Fryer, and C. J. Gilmore. "Electron Crystallography of a Metal Azo Salt Pigment." In Electron Crystallography, 367–70. Dordrecht: Springer Netherlands, 1997. http://dx.doi.org/10.1007/978-94-015-8971-0_33.

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Liu, Qing-Song, Wen-Qiang Lu, and Guan-Wu Wang. "Transition Metal Salt-Catalyzed Reactions of [60]Fullerene." In Handbook of Fullerene Science and Technology, 503–39. Singapore: Springer Nature Singapore, 2022. http://dx.doi.org/10.1007/978-981-16-8994-9_35.

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Freyland, W. "Metal-Molten Salt Interfaces: Wetting Transitions and Electrocrystallization." In Molten Salts: From Fundamentals to Applications, 149–77. Dordrecht: Springer Netherlands, 2002. http://dx.doi.org/10.1007/978-94-010-0458-9_5.

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Conference papers on the topic "SALT-METAL"

1

SATO, NOBUYUKI, YOSIHIKO OGANE, SHUICH SUGITA, MASAMI SHOYA, TERUO HIGA, and NAOMITU TUYUKI. "REDUCTION OF SALT AND HEAVY METAL USING MICROORGANISMS." In Proceedings of the 4th International Conference. WORLD SCIENTIFIC, 2004. http://dx.doi.org/10.1142/9789812702623_0164.

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Suzumura, Y., and T. Ogawa. "Metal-insulator transition in organic conductor DCNQI-Cu salt." In International Conference on Science and Technology of Synthetic Metals. IEEE, 1994. http://dx.doi.org/10.1109/stsm.1994.835545.

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Cassidy, Galen Patrick, and Donald C. Barber. "MONITORING TOXIC HEAVY METAL CONCENTRATIONS OF MASSACHUSETTS SALT MARSH SEDIMENTS." In Joint 69th Annual Southeastern / 55th Annual Northeastern GSA Section Meeting - 2020. Geological Society of America, 2020. http://dx.doi.org/10.1130/abs/2020se-343927.

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Kumar, K. Siva, B. Kavitha, K. Prabakar, D. Srinivasu, Ch Srinivas, and N. Narsimlu. "Synthesis and characterization of metal oxide-polyaniline emeraldine salt based nanocomposite." In SOLID STATE PHYSICS: PROCEEDINGS OF THE 57TH DAE SOLID STATE PHYSICS SYMPOSIUM 2012. AIP, 2013. http://dx.doi.org/10.1063/1.4790963.

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Wu, Zhaohui, Jingfu Bao, Yi Zhang, Yinglan Chen, and Xiaosheng Zhang. "Droplet Rapid-Analasis Method of Metal-Salt Solution Based on Triboelectric Effect." In 2019 20th International Conference on Solid-State Sensors, Actuators and Microsystems & Eurosensors XXXIII (TRANSDUCERS & EUROSENSORS XXXIII). IEEE, 2019. http://dx.doi.org/10.1109/transducers.2019.8808301.

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Zou, Zhi, Liqun Ma, Lei Qiao, Xiaochuan Gan, and Qiuqin Fan. "Feature recognition of metal salt spray corrosion based on color spaces statistics analysis." In Applications of Digital Image Processing XL, edited by Andrew G. Tescher. SPIE, 2017. http://dx.doi.org/10.1117/12.2273851.

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Wallraff, Gregory M., Hoa D. Truong, Martha I. Sanchez, Noel Arellano, Alexander M. Friz, Wyatt Thornley, Oleg Kostko, Dan S. Slaughter, and D. Frank Ogletree. "Model studies on the metal salt sensitization of chemically amplified photoresists (Conference Presentation)." In Advances in Patterning Materials and Processes XXXVI, edited by Roel Gronheid and Daniel P. Sanders. SPIE, 2019. http://dx.doi.org/10.1117/12.2514610.

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Saari, Riza, Ryosuke Tsuyuguchi, and Masayuki Yamaguchi. "Effect of metal salt incorporation on structure and properties for poly(vinyl alcohol)." In NOVEL TRENDS IN RHEOLOGY VIII. Author(s), 2019. http://dx.doi.org/10.1063/1.5109507.

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Abramov, A. V., V. V. Karpov, A. Yu Zhilyakov, S. V. Belikov, V. A. Volkovich, I. B. Polovov, and O. I. Rebrin. "Corrosion resistance of nickel-based alloys in salt and metal melts containing REE." In 3RD ELECTRONIC AND GREEN MATERIALS INTERNATIONAL CONFERENCE 2017 (EGM 2017). Author(s), 2017. http://dx.doi.org/10.1063/1.5002926.

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Praveena, S. D., V. Ravindrachary, Ismayil, R. F. Bhajantri, A. Harisha, B. Guruswamy, Shreedatta Hegde, and Rohan N. Sagar. "Inhibition and quenching effect on positronium formation in metal salt doped polymer blend." In DAE SOLID STATE PHYSICS SYMPOSIUM 2017. Author(s), 2018. http://dx.doi.org/10.1063/1.5028838.

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Reports on the topic "SALT-METAL"

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Sahai, Yogeshwar. Molten Metal Treatment by Salt Fluxing with Low Environmental Emissions. Office of Scientific and Technical Information (OSTI), July 2007. http://dx.doi.org/10.2172/912766.

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WILLIAM, WILMARTH. Reactivity of Crystalline Silicotitanate (CST) and Hazardous Metal/Actinide Loading During Low Curie Salt Use. Office of Scientific and Technical Information (OSTI), November 2004. http://dx.doi.org/10.2172/837909.

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Dermatas, D. Stabilization and reuse of heavy metal contaminated soils by means of quicklime sulfate salt treatment. Final report, September 1992--February 1995. Office of Scientific and Technical Information (OSTI), August 1995. http://dx.doi.org/10.2172/201739.

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Petrovic, Bojan, and Ivan Maldonado. Fuel and Core Design Options to Overcome the Heavy Metal Loading Limit and Improve Performance and Safety of Liquid Salt Cooled Reactors. Office of Scientific and Technical Information (OSTI), April 2016. http://dx.doi.org/10.2172/1253940.

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S. Frank. I-NERI ANNUAL TECHNICAL PROGRESS REPORT: 2006-002-K, Separation of Fission Products from Molten LiCl-KCl Salt Used for Electrorefining of Metal Fuels. Office of Scientific and Technical Information (OSTI), September 2009. http://dx.doi.org/10.2172/971358.

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