Relevant bibliographies by topics / Metallurgy - Ion exchange processes

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  1. Journal articles
  2. Dissertations / Theses
  3. Books
  4. Book chapters
  5. Conference papers
  6. Reports

Academic literature on the topic 'Metallurgy - Ion exchange processes'

Author: Grafiati
Published: 4 June 2021
Last updated: 2 February 2022

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Journal articles on the topic "Metallurgy - Ion exchange processes"

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Hubicki, Z., and M. Olszak. "Studies of the Effect of Crosslinking in the Strongly Basic Anion Exchanger Dowex 1 and the HNO3 Concentration Employed on the Separation of the SmIII–NdIII Pair in the Polar Organic Solvent–H2O–HNO3 System." Adsorption Science & Technology 19, no. 3 (April 2001): 219–28. http://dx.doi.org/10.1260/0263617011494105.

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Because of their specific structure, rare earth elements are used for the modification or structural stabilization of many metallic or ceramic materials employed in modern technology and also in the metallic form, i.e. in alloys and compounds with unique properties. Industrial demand for rare earth metals has increased lately due to their new application possibilities, e.g. in supermagnets of the Nd–Fe–B type or in ceramic high-temperature superconductors. Equally, the application of rare earth elements in metallurgy, catalysis, ceramics, etc. remains of significant importance. The separation and purification of rare earth elements(III) which occur in groups with similar physicochemical properties involve extremely difficult and complex processes. Ion exchange is one method which enables such separation. This paper presents the results of studies of the influence of the extent of crosslinking in the anion exchanger Dowex 1 and the concentration of nitric acid on the separation of the SmIII–NdIII pair by frontal analysis in 90% v/v CH3COCH3– or the CH3OH–10% v/v × M HNO3 systems. The most effective results were obtained in the 90% v/v CH3OH–10% v/v 7 M HNO3 system employing the anion exchanger Dowex 1 × 4 allowing 0.11 kg samarium(III) to be purified on 1 dm3 ion exchanger in the nitrate form and leading to a decrease in the micro-component content to a value below 10−3%.
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Dyer, A. "Ion-exchange processes." TrAC Trends in Analytical Chemistry 10, no. 1 (January 1991): 7–8. http://dx.doi.org/10.1016/0165-9936(91)85037-r.

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Sengupta, Arup K., and Lois Lim. "Modeling chromate ion-exchange processes." AIChE Journal 34, no. 12 (December 1988): 2019–29. http://dx.doi.org/10.1002/aic.690341211.

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Kedem, O., and L. Bromberg. "Ion-exchange membranes in extraction processes." Journal of Membrane Science 78, no. 3 (April 1993): 255–64. http://dx.doi.org/10.1016/0376-7388(93)80005-i.

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Hajiev, S. N., S. V. Kertman, U. A. Leykin, and A. N. Amelin. "Thermochemical study of ion-exchange processes." Thermochimica Acta 139 (March 1989): 327–32. http://dx.doi.org/10.1016/0040-6031(89)87032-7.

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Sherry, Howard. "The design of ion-exchange processes." Zeolites 13, no. 5 (June 1993): 377–83. http://dx.doi.org/10.1016/0144-2449(93)90153-t.

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Fernández, A., M. Díaz, and A. Rodrigues. "Kinetic mechanisms in ion exchange processes." Chemical Engineering Journal and the Biochemical Engineering Journal 57, no. 1 (March 1995): 17–25. http://dx.doi.org/10.1016/0923-0467(94)02865-8.

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Гомеля, М. Д., A. I. Петриченко, Г. Г. Трохименко, and Я. П. Мартинюк. "Research processes of ion exchange removal phosphates." WATER AND WATER PURIFICATION TECHNOLOGIES. SCIENTIFIC AND TECHNICAL NEWS 21, no. 1 (May 10, 2017): 12–23. http://dx.doi.org/10.20535/2218-93002112017121427.

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Ramkumar, Jayshree, and Tulsi Mukherjee. "Role of Ion exchange in permeation processes." Talanta 71, no. 3 (February 28, 2007): 1054–60. http://dx.doi.org/10.1016/j.talanta.2006.05.082.

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Slater, M. J. "Ion exchange and sorption processes in hydrometallurgy." Hydrometallurgy 20, no. 1 (March 1988): 131–32. http://dx.doi.org/10.1016/0304-386x(88)90033-3.

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Dissertations / Theses on the topic "Metallurgy - Ion exchange processes"

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Fernando, Kapila Chemical Sciences &amp Engineering Faculty of Engineering UNSW. "The treatment of cyanidation tailings using ion exchange resin." Awarded by:University of New South Wales. Chemical Sciences & Engineering, 2007. http://handle.unsw.edu.au/1959.4/40697.

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This thesis explores the behaviour of metal cyanide complexes under oxidative acid conditions in ion exchange systems, with the objective of developing an ion exchange based process for the treatment of gold cyanidation tailings. The novel cyanide detoxification process developed from this study employs strong base ion exchange resins to extract cyanide from tailings. Variations in the stability of cyanide complexes are exploited to concentrate, recover, or destroy cyanide species loaded on the resin, through the use of an oxidative acid eluent containing H2O2 and H2SO4. This eluent removes all base metal cyanide complexes from strong base resins, while regenerating the resin. The spent eluent, containing the base metals recovered from the tailings, can be used as a source of such base metals. Copper can be recovered separately from other base metals if necessary. Low levels of precious metals present in the tailings are accumulated on the resin as the ion exchange bed is cycled between loading and elution stages. They can be recovered economically, so as to offset the cost of the tailings detoxification. Cyanide is initially concentrated as an alkaline solution, which can be detoxified within the process or recovered for recycling. This process was successfully tested at pilot scale by treating approximately 14,000 m3 of cyanide contaminated tailings solution, over 14 loading/elution cycles on a standard strong base ion exchange resin bed. This treatment reduced the total cyanide concentration of the contaminated solution from approximately 50 mg/L to an average of 1.5 mg/L. The reagent cost was approximately ADD 0.50 per m3 of treated liquor. When the resin was repeatedly loaded with mixed metal cyanide species and eluted with the oxidative acid eluent, a gradual deterioration of the ion exchange resin performance was noted. The reduction of net operating capacity of the columns due to resin deterioration was in the order of 1-3% per loading/elution cycle. The oxidation of resin catalysed by copper, the precipitation of metal hexacyanoferrates on the resin and the oxidation of Au(CN)2- to Au(CN)4- were identified as possible factors giving rise to the reduction of resin loading capacity.
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El-Masri, Nasrein. "Ion-association complexes of thallium and mercury with rhodamine 6G in aqueous solution." Scholarly Commons, 1988. https://scholarlycommons.pacific.edu/uop_etds/2170.

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Van, Den Bosch Magali Marie. "Simulation of ion exchange processes using neuro-fuzzy reasoning." Thesis, Cape Peninsula University of Technology, 2009. http://hdl.handle.net/20.500.11838/2161.

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Thesis (MTech (Chemical Engineering))--Cape Peninsula University of Technology, 2009.
Neuro-fuzzy computing techniques have been approached and evaluated in areas of process control; researchers have recently begun to evaluate its potential in pattern recognition. Multi-component ion exchange is a non-linear process, which is difficult to model and simulate as there are many factors influencing the chemical process which are not well understood. In the past, empirical isotherm equations were used but there were definite shortcomings resulting in unreliable simulations. In this work, the use of artificial intelligence has therefore been researched to test the effectiveness in simulating ion exchange processes. The branch of artificial intelligence used was the adaptive neuro fuzzy inference system. The objective of this research was to develop a neuro-fuzzy software package to simulate ion exchange processes. The first step towards building this system was to collect data from laboratory scale ion exchange experiments. Different combinations of inputs (e.g. solution concentration, resin loading, impeller speed), were tested to determine whether it was necessary to monitor all available parameters. The software was developed in MSEXCEL where tools like SOLVER could be utilised whilst the code was written in Visual Basic. In order to compare the neuro-fuzzy simulations to previously used empirical methods, the Fritz and Schluender isotherm was used to model and simulate the same data. The results have shown that both methods were adequate but the neuro-fuzzyapproach was the more appropriate method. After completion of this study, it could be concluded that a neuro-fuzzy system does not always have the ability to describe ion exchange processes adequately.
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Steinwinder, Thomas Riemann Zhao Dongye. "Engineered treatment of As-laden regeneration brine from ion exchange processes." Auburn, Ala., 2006. http://repo.lib.auburn.edu/2006%20Spring/master's/STEINWINDER_THOMAS_33.pdf.

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Boulehdid, Hanae. "Elaboration et caractérisation d'une membrane cationique monosélective par modification chimique d'un film ETFE." Doctoral thesis, Universite Libre de Bruxelles, 2008. http://hdl.handle.net/2013/ULB-DIPOT:oai:dipot.ulb.ac.be:2013/210555.

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Ce travail porte sur l'amélioration de la sélectivité préférentielle d'une membrane cationique à base d’ETFE pour une utilisation en électrodialyse afin de traiter des effluents industriels contenant un mélange d’acides et de sels métalliques. Pour cela, nous avons fait appel à la méthode de la modification chimique de la surface d’une membrane cationique par la formation d’un film superficiel mince portant des charges positives afin de former une barrière de répulsion électrostatique pour des cations bivalents tout en permettant le passage de cations monovalents tels que les protons.

La synthèse de la membrane cationique de base a été réalisée en passant par différentes étapes à savoir :le greffage du styrène - divinylbenzène (DVB), la chlorosulfonation et l’hydrolyse.

Au cours de ce travail, nous avons mis au point un protocole de greffage du styrène-DVB dans le film d’ETFE qui permet l’obtention d’un film ayant un taux de greffage reproductible assurant à la membrane cationique finale une bonne conductivité électrique et une capacité d’échange acceptable pour une membrane d’électrodialyse. Une étude de la réaction de greffage en fonction de la concentration en réticulant a été réalisée.

Nous avons procédé par la suite à la modification de la surface du film d’ETFE greffé styrène-DVB par la formation d’une couche superficielle mince fixée par des liens covalents. Les membranes modifiées ont été obtenues par la réaction d’une seule face du film d’ETFE greffé chlorosulfoné avec la 3-diméthylaminopropylamine. La modification chimique de la surface du film ETFE greffé chlorosulfoné a été suivie par la technique FTIR-ATR. L’effet de la concentration de la diamine sur les propriétés électrochimiques des différentes membranes modifiées a été étudié. La résistance électrique des membranes modifiées équilibrées au contact de solutions de chlorure de sodium et d'acide sulfurique a été mesurée par la technique d’impédance. La détermination du nombre de transport du proton et de l’ion sodium a été réalisée à partir de mesures du potentiel de membrane. La densité de courant limite des membranes a été évaluée sur base des courbes courant-tension. Les mesures de chronopotentiométrie ont été également effectuées sur les différentes membranes synthétisées.

Les résultats de ces caractérisations montrent que la modification de la surface engendre des changements considérables au niveau des propriétés électrochimiques des membranes résultantes. La résistance électrique, la densité de courant limite ainsi que les propriétés de transport de la membrane dépendent d’une part de la concentration de la diamine utilisée et d’autre part de la solution dans laquelle la membrane modifiée est équilibrée.

La sélectivité préférentielle des différentes membranes vis-à-vis des protons par rapport aux ions bivalents a été testée en réalisant des électrodialyses d’un milieu mixte H2SO4-NiSO4. Nos résultats montrent que la modification chimique de la surface de la membrane affecte d’une manière significative le transport des ions nickel tout en respectant le passage des protons. Une meilleure séparation a été obtenue pour une membrane modifiée en utilisant la diamine pure.


Doctorat en Sciences
info:eu-repo/semantics/nonPublished

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Hastie, Michele. "Energy and Water Conservation in Biodiesel Purification Processes." Thèse, Université d'Ottawa / University of Ottawa, 2011. http://hdl.handle.net/10393/20384.

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Biodiesel purification processes generate wastewater streams that require a large amount of energy when distillation is used as a treatment technology. Process simulation software was used to show that an alternative water treatment process involving ion exchange would require only 31% of the energy used by distillation. Experiments showed that multiple washing stages were required to meet the standard specification for sodium, an impurity present in crude biodiesel, when washing biodiesel made from used frying oil. A comparison was made between washing biodiesel in a cross-current washing configuration and a counter-current configuration. Both configurations met the specification for sodium within three washing stages; however, the counter-current configuration required less water, making it the more efficient process. Lastly, the removal of sodium from wastewater samples using an ion exchange resin was experimentally investigated. The results validated the use of ion exchange to reduce energy consumption in biodiesel purification.
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Yip, Ngai Yin. "Sustainable Production of Water and Energy with Osmotically-Driven Membrane Processes and Ion-Exchange Membrane Processes." Thesis, Yale University, 2015. http://pqdtopen.proquest.com/#viewpdf?dispub=3582181.

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The world population of the 21st century is facing an increasingly challenging energy landscape and declining water quality and availability, further compounded by a rapidly expanding global population against the backdrop of climate change. To meet the challenges of the water-energy nexus in a sustainable manner, existing methods need to be advanced and new technologies developed. Osmotically-driven and ion-exchange membrane processes are two classes of emerging technologies that can offer cost-effective and environmentally sensible solutions to alleviate the pressure on our water and energy demands. The objective of this thesis is to advance forward osmosis (FO), pressure retarded osmosis (PRO), and reverse electrodialysis (RED) for the sustainable production of water and energy.

A main hindrance restricting the progress of osmotically-driven membrane processes, FO and PRO, is the absence of adequate membranes. This work demonstrates the fabrication of thin-film composite polyamide FO membranes that can attain high water flux and PRO membranes capable of achieving power density of 10 W/m2, twice the benchmark of 5 W/m2 for PRO with natural salinity gradients to be cost-effective. A membrane fabrication platform based on mechanistic understanding of the influence of membrane transport and structural parameters on process performance was developed. The morphology and microstructure of the porous support layer, and hydraulic permeability and salt selectivity of the polyamide active layer were specifically tailored by thoughtful control of the fabrication and modification conditions.

The Gibbs free energy from the mixing of river water with seawater can potentially be harnessed for clean and renewable energy production. This work analyzed the thermodynamics of PRO power generation and determined that energy efficiencies of up to ∼91% can theoretically be attained. The intrinsic limitations and practical constraints in PRO were identified and discussed. Using a tenth of the annual global river water discharge of 37,000 km 3 for PRO could potentially produce electricity for over half a billion people, ascertaining natural salinity gradients to be a sizeable renewable source that can contribute to diversifying our energy portfolio.

However, fouling of the membrane support layer can diminish the PRO productivity by detrimentally increasing the hydraulic resistance. Analysis of the water flux behavior and methodical characterization of the membrane properties shed light on the fouling mechanism and revealed the active-support layer interface to play a crucial role during fouling. A brief osmotic backwash was shown to be effective in cleaning the membrane and achieving substantial performance recovery.

Reverse electrodialysis (RED) is an ion-exchange membrane process that can also extract useful work from salinity gradients. This dissertation research examined the energy efficiency and power density of RED and identified a tradeoff relation between the two performance parameters. Energy efficiency of ∼33-44% can be obtained with technologically-available membranes, but the low power densities of < 1 W/m2 is likely to be impede the realization of the process. To further advance RED as a salinity energy conversion method, ion-exchange membrane technology and stack design need to be advanced beyond their current limitations.

When analyzed with simulated existing state-of-the-art membranes, PRO exhibited greater energy efficiencies (54-56%) and significantly higher power densities (2.4-38 W/m2) than RED (18-38% and 0.77-1.2 W/m 2). The drawback of RED is especially pronounced at large salinity gradients, where the high solution concentrations overwhelm the Donnan exclusion effect and detrimentally diminish the ion exchange membrane permselectivity. Additionally, the inherent different in driving force utilization (osmotic pressure difference for PRO and Nernst potential for RED) restricts RED from exploiting larger salinity gradients to enhance performance. Overall, PRO is found to be the more favorable membrane-based technology for accessing salinity energy.

This work presents pioneering advances for forward osmosis and pressure retarded osmosis membrane development. The fundamental studies of the osmotically-driven membrane processes and ion-exchange membrane processes yielded significant findings that enhanced our mechanistic and thermodynamic understanding of the technologies. The important insights can serve to inform the realization of the emerging membrane-based technologies for the sustainable production of water and energy. The implications of the thesis are potentially far-reaching and are anticipated to shape the discussion on FO, PRO, and RED.

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Tervonen, Ari. "Optical waveguides by ion exchange in glass fabrication processes for integrated optics applications /." Helsinki : Finnish Society of Sciences and Letters, 1990. http://catalog.hathitrust.org/api/volumes/oclc/35476660.html.

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Marinetti, Andrea. "Recovery of Carboxylic acids from anaerobic fermented broth through ionic exchange processes." Master's thesis, Alma Mater Studiorum - Università di Bologna, 2019.

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The recovery of Carboxylic acids were based on two particular objective: the study of the efficiency of a cation exchange resin, used in order to reduce the pH of the actual effluent, considering it is necessary to have a low pH for the anion exchange resin to be able to adsorb the acids from the effluent, and the preliminary studies perfomerd on the anion exchange resin, at various flow rates and both mode of operation, expanded and packed bed mode, using a simulated effluent, were the carboxylic acids were represented by just acetic acid, as the target molecule.
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Bhumgara, Zubin Godrej. "A study of the development of polyhipe foam materials for use in separation processes." Thesis, University of Exeter, 1995. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.263147.

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Books on the topic "Metallurgy - Ion exchange processes"

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Gritton, K. S. Numerical prediction of cobalt sorption in a continuous ion-exchange column. Pittsburgh, Pa: U.S. Dept. of the Interior, Bureau of Mines, 1987.

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Staker, W. L. Selective elution of mercury, silver, and gold from strong-base anion-exchange resins. Pittsburgh, Pa: U.S. Dept. of the Interior, Bureau of Mines, 1987.

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Fortin, C. Analysis of the complexing capacity of low-level radioactive waste leachates using an ion-exchange technique. Chalk River, Ont: Chalk River Laboratories, 1995.

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Ulewicz, Małgorzata. Separacja jonów metali nieżelaznych w procesie transportu przez ciekłe membrany zawierające związki makrocykliczne. Częstochowa: Wydawn. Wydziału Inżynierii Procesowej, Materiałowej i Fizyki Stosowanej, Politechniki Częstochowskiej, 2011.

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Ion-exchange membrane separation processes. Amsterdam: Elsevier, 2004.

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SenGupta, Arup K. Ion Exchange in Environmental Processes. Hoboken, New Jersey: John Wiley & Sons, Inc., 2017. http://dx.doi.org/10.1002/9781119421252.

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1937-, Brouillard F., and North Atlantic Treaty Organization. Scientific Affairs Division., eds. Atomic processes in electron-ion and ion-ion collisions. New York: Plenum Press, 1986.

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Vasilʹevich, Mokhosoev Marks, Zonkhoeva Ė L, and Lebedev K. B, eds. Modifit͡s︡irovannye ionity v tekhnologii molibdena i volʹframa. Novosibirsk: Izd-vo "Nauka," Sibirskoe otd-nie, 1985.

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A, Brown Richard. Impact of anion exchange pre-treatment on downstream processes. Denver, CO: Water Research Foundation, 2011.

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Altringer, P. B. Recovery of tungsten from Searles Lake brines by an ion-exchange process. [Avondale, Md.]: U.S. Dept. of the Interior, Bureau of Mines, 1985.

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Book chapters on the topic "Metallurgy - Ion exchange processes"

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Chen, J. Paul, Lei Yang, Wun-Jern Ng, Lawrence K. Wang, and Sook-Leng Thong. "Ion Exchange." In Advanced Physicochemical Treatment Processes, 261–92. Totowa, NJ: Humana Press, 2006. http://dx.doi.org/10.1007/978-1-59745-029-4_8.

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Nasef, Mohamed Mahmoud, and Zaini Ujang. "Introduction to Ion Exchange Processes." In Ion Exchange Technology I, 1–39. Dordrecht: Springer Netherlands, 2012. http://dx.doi.org/10.1007/978-94-007-1700-8_1.

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Kimizuka, H., Y. Nagata, and W. Yang. "Ion and Solvent Transports Through Amphoteric Ion Exchange Membrane." In Membranes and Membrane Processes, 85–92. Boston, MA: Springer US, 1986. http://dx.doi.org/10.1007/978-1-4899-2019-5_10.

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Carrà, Sergio. "Reaction Processes Involving Ion-Exchange Resins." In Ion Exchange: Science and Technology, 485–511. Dordrecht: Springer Netherlands, 1986. http://dx.doi.org/10.1007/978-94-009-4376-6_18.

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Scott, K. "Ion-exchange and charge driven processes." In Industrial Membrane Separation Technology, 181–257. Dordrecht: Springer Netherlands, 1996. http://dx.doi.org/10.1007/978-94-011-0627-6_7.

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Dunn, K. F. "Charge Exchange and Ionisation in Collisions Between Positive Ions." In Atomic Processes in Electron-Ion and Ion-Ion Collisions, 333–56. Boston, MA: Springer US, 1986. http://dx.doi.org/10.1007/978-1-4684-5224-2_12.

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Meares, Patrick. "Ion Exchange Membranes: Principles, Production and Processes." In Ion Exchange: Science and Technology, 529–58. Dordrecht: Springer Netherlands, 1986. http://dx.doi.org/10.1007/978-94-009-4376-6_20.

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Janev, R. K. "Theory of Charge Exchange and Ionization in Ion-Atom (Ion) Collisions." In Atomic Processes in Electron-Ion and Ion-Ion Collisions, 239–69. Boston, MA: Springer US, 1986. http://dx.doi.org/10.1007/978-1-4684-5224-2_9.

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Williams, Robert J. P. "The Importance of Ion Exchange Processes in Living Systems." In Recent Developments in Ion Exchange, 3–15. Dordrecht: Springer Netherlands, 1990. http://dx.doi.org/10.1007/978-94-009-0777-5_1.

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Tondeur, D., and G. Grevillot. "Parametric Ion-Exchange Processes (Parametric Pumping and Allied Techniques)." In Ion Exchange: Science and Technology, 369–99. Dordrecht: Springer Netherlands, 1986. http://dx.doi.org/10.1007/978-94-009-4376-6_14.

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Conference papers on the topic "Metallurgy - Ion exchange processes"

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Trassl, R. "Ion-ion charge-exchange collisions and applications." In The 12th topical conference on atomic processes in plasmas. AIP, 2000. http://dx.doi.org/10.1063/1.1361787.

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Tervonen, A., S. Honkanen, and M. Leppihalme. "Ion-Exchange Processes In Glass For Fabrication Of Waveguide Couplers." In 1987 Symposium on the Technologies for Optoelectronics, edited by Giancarlo C. Righini and Oliverio D. Soares. SPIE, 1988. http://dx.doi.org/10.1117/12.943465.

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Oya, Takumi, and Suguru Sassa. "Development of ion exchange purification for advanced materials contain siloxane polymer." In Advances in Patterning Materials and Processes XXXVII, edited by Roel Gronheid and Daniel P. Sanders. SPIE, 2020. http://dx.doi.org/10.1117/12.2553654.

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Zelenskii, A. N., S. A. Kokhanovskii, V. G. Polushkin, and K. N. Vishnevskii. "Investigation of spin-exchange processes in the optically polarized ion source." In Production and neutralization of negative ions and beams. AIP, 1990. http://dx.doi.org/10.1063/1.39614.

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Prieto, Xesus, Jesus Linares, and Carlos Montero. "Perturbative method to modelize ion-exchange processes: application to surface waveguides." In Advanced Imaging and Network Technologies, edited by Giancarlo C. Righini. SPIE, 1996. http://dx.doi.org/10.1117/12.262449.

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Shu-Yin Tsao and Chao-Yi Tai. "The development of nano-structured plasmonic composite by two-step ion-exchange processes." In 2012 IEEE 12th International Conference on Nanotechnology (IEEE-NANO). IEEE, 2012. http://dx.doi.org/10.1109/nano.2012.6322190.

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Meychik, N. R., Yu I. Nikolaeva, and M. A. Kushunina. "Ion-exchange properties of root cell walls and their significance for some physiological processes." In IX Congress of society physiologists of plants of Russia "Plant physiology is the basis for creating plants of the future". Kazan University Press, 2019. http://dx.doi.org/10.26907/978-5-00130-204-9-2019-285.

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Miron, Alexandra Raluca. "USE OF ION EXCHANGE PROCESSES ON WEAK ACID RESINS FOR NICKEL REMOVAL FROM WASTE WATERS." In 15th International Multidisciplinary Scientific GeoConference SGEM2015. Stef92 Technology, 2011. http://dx.doi.org/10.5593/sgem2015/b51/s20.133.

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Marzuki, Ahmad, Seran Daton Gregorius, Ika Widhianingsih, Siti Lestari, and Joko Suryawan. "Planar optical waveguides fabricated by Ag+/K+-Na+ ion exchange in soda lime glass." In INTERNATIONAL CONFERENCE OF CHEMICAL AND MATERIAL ENGINEERING (ICCME) 2015: Green Technology for Sustainable Chemical Products and Processes. AIP Publishing LLC, 2015. http://dx.doi.org/10.1063/1.4938319.

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Chungyi Chou, Yuehwa Yu, Chingyuan Chang, Chengfang Lin, and Nengchou Shang. "The combination of ozonation and ion exchange processes for treatment of a municipal wastewater plant effluent." In 2011 International Conference on Electric Technology and Civil Engineering (ICETCE). IEEE, 2011. http://dx.doi.org/10.1109/icetce.2011.5775819.

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Reports on the topic "Metallurgy - Ion exchange processes"

1

Wallace, R. M. Ion Exchange Membrane Processes. Office of Scientific and Technical Information (OSTI), October 2002. http://dx.doi.org/10.2172/804675.

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McGrail, B. P., D. K. Shuh, J. G. Darab, and D. R. Baer. Ion-exchange processes and mechanisms in glasses. Office of Scientific and Technical Information (OSTI), June 1998. http://dx.doi.org/10.2172/13687.

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McGrail, B. Peter, D. R. Baer, J. G. Darab, j. p. Icenhower, and D. K. Shuh. Ion Exchange Processes and Mechanisms in Glasses. Office of Scientific and Technical Information (OSTI), June 2000. http://dx.doi.org/10.2172/829972.

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McGrail, B. P., J. P. Icenhower, J. G. Darab, D. k. Shuh, D. R. Baer, V. Shutthanandan, S. Thevuthasan, et al. Ion-Exchange Processes and Mechanisms in Glasses. Office of Scientific and Technical Information (OSTI), December 2001. http://dx.doi.org/10.2172/830030.

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McGrail, B. Peter, and David K. Shuh. Ion-Exchange Processes and Mechanisms in Glasses. Office of Scientific and Technical Information (OSTI), June 1999. http://dx.doi.org/10.2172/829970.

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Espinoza, Jacob, Mary Barr, and Wayne Smith. Denitration of Rocky Flats Ion-Exchange Resins: Recommendation of Denitration Processes, October 19, 1995. Office of Scientific and Technical Information (OSTI), December 1998. http://dx.doi.org/10.2172/2610.

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