Relevant bibliographies by topics / Phosphonic acid

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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 'Phosphonic acid'

Author: Grafiati
Published: 4 June 2021
Last updated: 25 July 2025

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Journal articles on the topic "Phosphonic acid"

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Maurya, Sandip, Katie Lim, Zhendong Hu, Hongfei Jia, Jeffrey Michael Klein, and Yu Seung Kim. "Alkyl Phosphonic Acids: An Alternative to Phosphoric Acid in HT-Pemfcs." ECS Meeting Abstracts MA2022-02, no. 41 (2022): 1510. http://dx.doi.org/10.1149/ma2022-02411510mtgabs.

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Phosphoric acid has received the most attention as a choice of electrolyte for a high-temperature proton exchange membrane fuel cell (HT-PEMFC). Phosphoric acid has many attractive properties such as high anhydrous conductivity, good compatibility with hydrocarbon membranes, and thermal stability [1], which enables high fuel cell performance under anhydrous and elevated operating temperatures (140-180 oC) [2-3]. However, phosphoric acid has undesirable properties such as high catalyst poisoning, high evaporation rate at > 200 oC, and low acid retention from the doped membrane. Alkyl phospho
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Weinberger, Christian, Tatjana Heckel, Patrick Schnippering, et al. "Straightforward Immobilization of Phosphonic Acids and Phosphoric Acid Esters on Mesoporous Silica and Their Application in an Asymmetric Aldol Reaction." Nanomaterials 9, no. 2 (2019): 249. http://dx.doi.org/10.3390/nano9020249.

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The combined benefits of moisture-stable phosphonic acids and mesoporous silica materials (SBA-15 and MCM-41) as large-surface-area solid supports offer new opportunities for several applications, such as catalysis or drug delivery. We present a comprehensive study of a straightforward synthesis method via direct immobilization of several phosphonic acids and phosphoric acid esters on various mesoporous silicas in a Dean–Stark apparatus with toluene as the solvent. Due to the utilization of azeotropic distillation, there was no need to dry phosphonic acids, phosphoric acid esters, solvents, or
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Arunagiri, Karthik, Andrew Jark-Wah Wong, Luis A. Briceno-Mena, Michael John Janik, Jose A. Romagnoli, and Christopher G. Arges. "Deconvolution of Charge-Transfer, Mass Transfer, and Ohmic Resistances of Phosphonic Acid-Sulfonic Acid Ionomer Binders in Electrochemical Hydrogen Pumps." ECS Meeting Abstracts MA2023-02, no. 39 (2023): 1928. http://dx.doi.org/10.1149/ma2023-02391928mtgabs.

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Ion-pair high-temperature polymer electrolyte membranes (HT-PEMs) paired with phosphonic acid ionomer electrode binders have substantially improved the performance of HT-PEM electrochemical hydrogen pumps (EHPs)1, 2 and fuel cells3. Recently, blending poly(pentafluorstyrene-co-tetrafluorostyrene phosphonic acid) (PTFSPA) with NafionTM improved ionomer conductivity under anhydrous conditions in the temperature range of 100 °C to 250 °C. Using the said polymer blend as an electrode binder resulted in a 2 W.cm-2 peak power density of fuel cells4 at 240 °C (a HT-PEM fuel cell record). However, muc
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Khanvilkar, Aditya N., and Ashutosh V. Bedekar. "Synthesis and characterization of chiral aza-macrocycles and study of their enantiomer recognition ability for organo-phosphoric acid and phosphonic acid derivatives by 31P NMR and fluorescence spectroscopy." Organic & Biomolecular Chemistry 14, no. 9 (2016): 2742–48. http://dx.doi.org/10.1039/c5ob02616d.

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Two diastereomers of optically active N,O-containing new macrocycles with dual chirality were synthesized and evaluated for chiral discrimination of organo phosphoric and phosphonic acids by <sup>31</sup>P NMR and fluorescence spectroscopy.
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Turgis, Raphaël, Antoine Leydier, Guilhem Arrachart, et al. "Uranium Extraction from Phosphoric Acid Using Bifunctional Amido-Phosphonic Acid Ligands." Solvent Extraction and Ion Exchange 32, no. 5 (2014): 478–91. http://dx.doi.org/10.1080/07366299.2014.898435.

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Bruckmann, J., C. Krüger, C. W. Lehmann, W. Leitner, J. Rust, and C. Six. "Ethylenebis(phosphonic acid)." Acta Crystallographica Section C Crystal Structure Communications 55, no. 4 (1999): 695–96. http://dx.doi.org/10.1107/s0108270198016448.

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Köken, Nesrin. "Polymers containing amino bis(methylene phosphonic acid) groups for scale inhibition." Pigment & Resin Technology 48, no. 1 (2019): 73–83. http://dx.doi.org/10.1108/prt-01-2017-0007.

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Purpose The purpose of this paper is to prepare poly[allyl amino bis(methylene phosphonic acid)-ran-acrylic acid]s by two different routes. In the first route, poly(allyl amine-ran-acrylic acid)s were produced by radical copolymerization of a mixture of ally amine and acrylic acid, then converted into poly[allyl amino bis(methylene phosphonic acid)-ran-acrylic acid]s by the Mannich reaction with a mixture of formaldehyde and phosphonic acid. In the second route, allyl amino bis(methylene phosphonic acid) monomer was synthesized and copolymerised with acrylic acid. The aim of this work is to pr
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Sevrain, Charlotte M., Mathieu Berchel, Hélène Couthon, and Paul-Alain Jaffrès. "Phosphonic acid: preparation and applications." Beilstein Journal of Organic Chemistry 13 (October 20, 2017): 2186–213. http://dx.doi.org/10.3762/bjoc.13.219.

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The phosphonic acid functional group, which is characterized by a phosphorus atom bonded to three oxygen atoms (two hydroxy groups and one P=O double bond) and one carbon atom, is employed for many applications due to its structural analogy with the phosphate moiety or to its coordination or supramolecular properties. Phosphonic acids were used for their bioactive properties (drug, pro-drug), for bone targeting, for the design of supramolecular or hybrid materials, for the functionalization of surfaces, for analytical purposes, for medical imaging or as phosphoantigen. These applications are c
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Su, Debao, Cai Yun Guo, Roger D. Willett, Brian Scott, Robert L. Kirchmeier, and Jean'ne M. Shreeve. "Synthesis of trans-1,2-difluoroethenediylbis(phosphonic acid) and other unsaturated phosphonic acids." Journal of the American Chemical Society 112, no. 8 (1990): 3152–55. http://dx.doi.org/10.1021/ja00164a042.

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Paladini, A., C. Calcagni, T. Di Palma та ін. "Laser production of gas phase complexes of metalα-aminophosphonic acid mixtures and their role in chiral recognition". International Journal of Photoenergy 3, № 4 (2001): 217–21. http://dx.doi.org/10.1155/s1110662x01000290.

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Clusters between first-group metal ions and chiralα-aminophosphonic acids have been readily generated by Pulsed Laser Ablation (PLA) and by Electrospray Ionization (ESI) and their fragmentation investigated by mass spectrometry. The complexes studied have the general formula[Me(I)Cl2]+, where Me(I) is H, Li, Na, or K, C is (R)-(—)-(1-aminoethyl) phosphonic acid(ER)and (S)-(+)-(1-aminoethyl) phosphonic acid(ES),(1R)-(+)-(1-amino-2-methylpropyl) phosphonic acid(PR)and (1S)-(—)-(1-amino-2-methylpropyl) phosphonic acid(PS),(1R)-(-)-(1-amino-hexyl) phosphonic acid (HR) and (1S)-(+)-(1-amino-hexyl)
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Dissertations / Theses on the topic "Phosphonic acid"

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McNichols, Brett William. "Synthesis and Application of Styryl Phosphonic and Cinnamic Acid Derivatives." Thesis, Colorado School of Mines, 2017. http://pqdtopen.proquest.com/#viewpdf?dispub=10624231.

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<p> Styryl phosphonic and cinnamic acid derivatives have been gaining attention as key candidates to modulate specific electrode properties in organic electronic devices such as work function, surface energies, wettability, and electron charge transfer kinetics that lead to increased efficiency, operational range, and device lifetimes. Very few of these acids are commercially available. The driving factor behind this research is to explore simple, high yield, and inexpensive synthetic routes towards synthesis of these acids. Herein, the novel synthesis of vinyl phosphonic acids (VPAs) and thei
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Oquendo, Galarza Luis E. "Modification of Indium Tin Oxide Surfaces with Phosphonic Acid Functionalized Phthalocyanines." Diss., The University of Arizona, 2014. http://hdl.handle.net/10150/344225.

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The overall efficiency of organic photovoltaics cells (OPVs) is influenced by the nature of the charge injection barrier at the transparent conducting oxide (TCO) bottom contact. Modification of the transparent conducting oxide (TCO)/organic interface with an electroactive molecular monolayer will potentially create a robust ohmic contact that will influence the efficiency of hole injection into the TCO. Asymmetric zinc Phthalocyanines (ZnPc) with a flexible phosphonic acid (PA) linker have been synthesized and used to modify indium tin oxide (ITO) surfaces. The adsorption of PA functionalized
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Centrone, Charla Anne. "Synthesis of C-phosphonic acid, C-phosphinic acid, and C-sulfone analogs of decaprenolphosphoarabinose inhibitors of mycobacterial arabinosyltransferases /." Connect to this title online, 2003. http://rave.ohiolink.edu/etdc/view?acc%5Fnum=osu1054062979.

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Thesis (Ph. D.)--Ohio State University, 2003.<br>Document formatted into pages; contains xvi, 371 p.; also contains graphics. Includes bibliographical references. Abstract available online via OhioLINK's ETD Center; full text release delayed at author's request until 2005 May 5.
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Sebah, Majda. "Novel Synthetic and Evaluation Studies on Phosphonic Acid Functlonalised Periodic Hybrid Materials." Thesis, Queen Mary, University of London, 2010. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.520461.

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Hotchkiss, Peter J. "The design, synthesis, and use of phosphonic acids for the surface modification of metal oxides." Diss., Atlanta, Ga. : Georgia Institute of Technology, 2008. http://hdl.handle.net/1853/31836.

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Thesis (Ph.D)--Chemistry and Biochemistry, Georgia Institute of Technology, 2009.<br>Committee Chair: Marder, Seth; Committee Member: Bredas, Jean-Luc; Committee Member: Kroger, Nils; Committee Member: Perry, Joe; Committee Member: Sandhage, Ken. Part of the SMARTech Electronic Thesis and Dissertation Collection.
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Senior, Geoffrey David. "The role of dissolved metal ionic species in the phosphonic acid flotation of cassiterite." Thesis, University of British Columbia, 1987. http://hdl.handle.net/2429/27527.

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The techniques of X-ray photoelectron spectroscopy (XPS), secondary ionization mass spectroscopy, chemical abstraction analysis and microelectrophoresis were used to confirm the existence of iron films on cassiterite grains recovered from the tin concentrator of Renison Limited (Australia). All analyses indicated the level of surface iron contamination to be far in excess of that characteristic of the bulk mineral lattice. No evidence was found in XPS analyses to support the contention that this iron represented lattice iron that had accumulated on the surface due to migration through the latt
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Wood, Christopher Alan. "Theoretical investigation of polar zinc oxide surface modification via phosphonic acid self-assembled monolayers." Thesis, Georgia Institute of Technology, 2012. http://hdl.handle.net/1853/43584.

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The interface of a zinc-terminated polar zinc oxide surface (0002) with a series of chemisorbed fluorinated benzylphosphonic acids has been studied using density functional theory. The calculations indicate that there is a substantial change in the binding energies and work function modification depending on the binding motif. The results also indicate that there is a pronounced difference in the magnitude and trends of the factors determining the total change in work function. The oxygen core-level binding shifts have been calculated and compared to available experimental data.
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Labalme, Etienne. "Synthesis and characterizations of new fluorinated membranes bearing pendant phosphonic acid groups for PEMFC application." Thesis, Montpellier, Ecole nationale supérieure de chimie, 2013. http://www.theses.fr/2013ENCM0013.

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Ce travail de thèse s'inscrit dans la continuité des travaux de recherche réalisés sur le développent de nouvelles membranes échangeuses de protons pour piles à combustibles de type PEMFC, porteuses de groupements protogènes acides phosphoniques. L'objectif de ces travaux est d'apporter des solutions permettant l'amélioration des propriétés physico-chimiques d'un copolymère phosphoné, le poly(CTFE-alt-VEPA) obtenu à partir de la polymérisation radicalaire de vinyl éthers et de CTFE. La première stratégie employée est une stratégie Blend. Elle consiste à ajouter un polymère fluoré commercial, l
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Helfrich, Marcus Robert. "Preliminary investigations into the development of novel layered phosphonic acid vesicles for targeted drug delivery applications /." view abstract or download file of text, 2002. http://wwwlib.umi.com/cr/uoregon/fullcit?p3045088.

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Thesis (Ph. D.)--University of Oregon, 2002.<br>Typescript. Includes vita and abstract. Includes bibliographical references (leaves 184-193). Also available for download via the World Wide Web; free to University of Oregon users. Address: http://wwwlib.umi.com/cr/uoregon/fullcit?p3045088.
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Wells, Christopher J. "The equilibrium characteristics of aqueous cobalt and nickel mixtures with the extractant bis-(2-ethylhexyl)-phosphonic acid." Thesis, University of Ottawa (Canada), 1991. http://hdl.handle.net/10393/7545.

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In this work, binary solutions of cobalt and nickel in aqueous ammonium sulfate solutions were extracted using a simple shake-out technique with a mixed organic phase consisting of the extractant bis-(2-ethylhexyl)phosphonic acid (PC-88A), the modifier tributyl phosphate, and the diluent Esso Varsol DX3641. It was found that the optimum pH for the separation of cobalt and nickel was 5.0, and that the separation of the ions was a complex function of the porportion of cobalt and nickel in the equilibrium phases. The maximum metal loading of the organic phase, based on the population of dimer ext
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Books on the topic "Phosphonic acid"

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P, Kukharʹ V., ed. Aminophosphonic and aminophosphinic acids: Chemistry and biological activity. Wiley, 2000.

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University, Iowa, ed. Synthesis of novel fluorinated phosphonic acid electroly for phosphoric acid fuel cells. Final report, January 1s1989-June 30, 1991. Iowa Univ., 1992.

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Frazier, A. W. Redistribution of impurities in wet-process phosphoric acid / A.W. Frzier, Y.K. Kim. National Fertilizer Development Center, Tennessee Valley Authority, 1988.

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Federal Energy Technology Center (U.S.), ed. Phosphoric acid fuel cell commercialization. U.S. Dept. of Energy, Office of Fossil Energy, Federal Energy Technology Center, 1998.

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El-Razik, Salah Mahrose Abd. Extraction of phosphoric acid from phosphateore. University of Salford, 1990.

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Hanrahan, Jane. The synthesis of substituted phosphonic acids. typescript, 1995.

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J, Kohler John, and National Fertilizer & Environmental Research Center (U.S.), eds. Aluminum removal from phosphoric acid as chukhrovite. National Fertilizer and Environmental Research Center, Tennessee Valley Authority, 1992.

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Norwood, Verrill M. Characterization of flourine-, aluminum-, silicon-, and phosphorus-containing complexes in wet-process phosphoric acid using nuclear magnetic resonance spectroscopy. Chemical Research, Tennessee Valley Authority, National Fertilizer Development Center, 1989.

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J, Fantel R., and United States. Bureau of Mines., eds. Phosphate availability and supply: A minerals availability appraisal. U.S. Dept. of the Interior, Bureau of Mines, 1988.

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1870-1925, Lang W. R., ed. The determination of boric acid, alone, and in the presence of phosphoric acid. University Library, pub. by the Librarian, 1997.

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Book chapters on the topic "Phosphonic acid"

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Bährle-Rapp, Marina. "Aminotrimethylene Phosphonic Acid." In Springer Lexikon Kosmetik und Körperpflege. Springer Berlin Heidelberg, 2007. http://dx.doi.org/10.1007/978-3-540-71095-0_506.

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Bährle-Rapp, Marina. "Diethylenetriamine Pentamethylene Phosphonic Acid." In Springer Lexikon Kosmetik und Körperpflege. Springer Berlin Heidelberg, 2007. http://dx.doi.org/10.1007/978-3-540-71095-0_2936.

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Jyo, Akinori, Kenji Okada, Masao Tamada, Tamikazu Kume, Takanobu Sugo, and Masato Tazaki. "Bifunctional Cation Exchange Fibers Having Phosphonic and Sulfonic Acid Groups." In Chemistry for the Protection of the Environment 4. Springer US, 2005. http://dx.doi.org/10.1007/0-387-27448-0_4.

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Phuc, Dang Hoang, Thi-Hiep Nguyen, Vo Van Toi, and Phan Van Tien. "Fabrication of Hyaluronan – Chitosan – Polyvinyl Phosphonic Acid Hydrogel for Bioglue Applications." In IFMBE Proceedings. Springer International Publishing, 2015. http://dx.doi.org/10.1007/978-3-319-11776-8_80.

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Wei, Zhang, Lu Xinchun, Liu Yuhong, Pan Guoshun, and Luo Jianbin. "Chemical Mechanical Polishing of Copper in Organic Phosphonic Acid System Slurry." In Advanced Tribology. Springer Berlin Heidelberg, 2009. http://dx.doi.org/10.1007/978-3-642-03653-8_310.

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Paszternák, A., Ilona Felhősi, Z. Keresztes, and Erika Kálmán. "Formation and Structure of Alkyl-Phosphonic Acid Layers on Passive Iron." In Materials Science Forum. Trans Tech Publications Ltd., 2007. http://dx.doi.org/10.4028/0-87849-426-x.239.

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Franck, Fabrice, Olga Górnicka, and Kazimierz Strzałka. "Effect of Phosphonic Acid Esters on Photoconversion of Protochlorophyllide in Barley Etioplasts." In Regulation of Chloroplast Biogenesis. Springer US, 1992. http://dx.doi.org/10.1007/978-1-4615-3366-5_33.

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Tuan, Le Quoc, Dang Hoang Phuc, Vo Van Toi, and Thi-Hiep Nguyen. "Fabrication of In Situ Cross-Linking Polyvinyl Phosphonic Acid - Chitosan Hydrogel for Wound Applications." In IFMBE Proceedings. Springer International Publishing, 2015. http://dx.doi.org/10.1007/978-3-319-11776-8_77.

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Winkelmann, Jochen. "Diffusion coefficient of P-(2-ethylhexyl)-phosphonic acid mono-(2-ethylhexyl)ester in heptane." In Diffusion in Gases, Liquids and Electrolytes. Springer Berlin Heidelberg, 2018. http://dx.doi.org/10.1007/978-3-662-54089-3_1093.

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Zhou, Limin, Hongbin Zou, Jieyun Jin, Zhirong Liu, and Taian Luo. "Preparation of phosphonic acid-functionalized silica magnetic microspheres for uranium(VI) adsorption from aqueous solutions." In Advances in Energy and Environment Research. CRC Press, 2017. http://dx.doi.org/10.1201/9781315212876-22.

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Conference papers on the topic "Phosphonic acid"

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Amjad, Zahid, and Amannie Kweik. "Formation and Control of Iron-Based Deposits in Industrial Water Systems." In CORROSION 2016. NACE International, 2016. https://doi.org/10.5006/c2016-07591.

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Abstract In this work, the performance of phosphonates as ferric (Fe3+) ions stabilization and iron oxide (Fe2O3) dispersing agents for aqueous system has been investigated. The phosphonates tested include: 2-hydroxyphosphono acetic acid (HPA), 1-hydroxyethylidine 1,1-diphosphonic acid (HEDP), aminotris (methylene phosphonic acid) (AMP), 2-phosphono-butane 1,2,4-tricarboxylic acid (PBTC), and polyamino polyether methylene phosphonic acid (PAPEMP). Results suggest that performance of phosphonates strongly depends on several factors including phosphonate concentration, reaction time, and phospho
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Hamdi, Mohab, Amannie Kweik, Ahmad Almakrani, and Zahid Amjad. "Extending Phosphonates Performance in Simulated Cooling Waters." In CORROSION 2018. NACE International, 2018. https://doi.org/10.5006/c2018-11054.

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Abstract Organic phosphonates are a family of compounds widely used as mineral scale and corrosion inhibitors in a variety of applications in industrial processes. The phenomena of scale and corrosion inhibition has been studied extensively. This study reports the tolerance of phosphonates with hardness ions under a variety of test conditions (i.e., temperature, type and concentration of hardness ions, total dissolved solids, etc.). The phosphonates tested include: hydroxyphosphono acetic acid, HPA; aminotris(methylene phosphonic acid), AMP; 1-hydroxyethylidine 1,1-diphosphonic acid, HEDP; 2-p
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Cushner, M. C., J. L. Przybylinski, and J. W. Ruggeri. "How Temperature and pH Affect the Performance of Barium Sulfate Inhibitors." In CORROSION 1988. NACE International, 1988. https://doi.org/10.5006/c1988-88428.

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Abstract Carbon dioxide flooding is an Enhanced Oil Recovery (EOR) technique which has become more widespread in recent years. This technique often causes the reservoir fluids to become more acidic. This may result in difficulty in controlling barium sulfate deposition problems which were formerly manageable. Investigations employing seeded crystal growth tests and capillary blocking tests were carried out with simulated oilfield brines near pH 4 and pH 7 at 40°C and 80°C. This was done to demonstrate how temperature and pH affect the efficiency of barium sulfate inhibitors. Saturation Indices
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Carvalho, Larissa A., Gabriel B. Leoni, Jussara de M. Silva, et al. "Study of Aminophosphonic Acid Molecules as Corrosion Inhibitors." In CONFERENCE 2025. AMPP, 2025. https://doi.org/10.5006/c2025-00448.

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Abstract Some common corrosion and scale inhibitors possess similar molecular features, such as Lewis bases functional groups, which allow them to adsorb onto metal surfaces, minimizing scale and/or corrosion processes. Even though both types of inhibitors are indispensable for correct oil &amp; gas operations, there is a technological gap about how one can act as the other, especially in an aggressive medium as produced water. Thus, the present work evaluated the corrosion protection given by two commercially employed scale inhibitors (i) Diethylene Triamine-Pentamethylene Phosphonic Acid (DT
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Mansfeld, F., A. T. Allen, and M. W. Kendig. "An Impedance Spectroscopy Study of Corrosion Inhibition in Neutral, Aerated Media." In CORROSION 1985. NACE International, 1985. https://doi.org/10.5006/c1985-85377.

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Abstract Impedance spectra have been determined over a wide frequency range for 4340 steel rotating cylinder electrodes in Na2SO4, NaCl, tap water and deionized water containing NaNO2, Na2Cr4O7 and a mixture of phosphonic acid or polyacrylic acid with fatty amine as inhibitors. For systems with low corrosion rates (Rp ⩾ 106 Ω·cm2), measurements have to be extended to very low frequencies. From the frequency dependence of the impedence, important information concerning the mechanism of corrosion inhibition can be obtained. For the phosphonic acid/fatty amine inhibitor in NaCl and Na2SO4, it has
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Demadis, Konstantinos D., Argyro Spinthaki, Michaela Kamaratou, et al. "Control of Metal Silicate Scaling by Chemical Additives." In CORROSION 2019. NACE International, 2019. https://doi.org/10.5006/c2019-12863.

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Abstract Metal silicate deposits have been noted in several water treatment facilities, but they are more common in geothermal systems. Herein, chemical approaches for the inhibition of metal silicate formation will be presented, focusing on two silicate scales, namely, magnesium and aluminum silicate. First, results will reveal the true nature of these scales. Then, results will be presented on the inhibitory effect of several chemical additives. The additives evaluated are (poly)phosphonic acids. They are PBTC (2-phosphonobutane-1,2,4-tricarboxylic acid), HEDP (hydroxyethylidene-1,1-diphosph
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Feeney, Thomas J., Julian Petry, Abderrezak Torche, et al. "Understanding and Exploiting Interfacial Interactions Between Phosphonic Acid Functional Groups and Co-Evaporated Perovskites." In 2024 IEEE 52nd Photovoltaic Specialist Conference (PVSC). IEEE, 2024. http://dx.doi.org/10.1109/pvsc57443.2024.10749030.

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Groysman, A. "Protection of Structures from Corrosion in Wastes." In CORROSION 1992. NACE International, 1992. https://doi.org/10.5006/c1992-92430.

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Abstract The protective properties of waste- and atmosphere- resistant paint coatings (with rust converters) have been studied in laboratory and field conditions and have been examined at the purification installations for a long time (5-7 years). The protective properties of organic (NTPh - Nitrilo Trimethylene Phosphonic Acid, OEDPh - Oxy Ethylidene DiPhosphonic Acid, mixtures of aliphatic acids - wastes of petroleum manufacturing) and inorganic (phosphates, borates and some peroxosalts) corrosion inhibitors on carbon steel used for wastes of refineries and petroleum distributor enterprises
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Ko, Saebom, Yi-Tsung Lu, Xin Wang, Amy T. Kan, Chong Dai, and Mason B. Tomson. "Deposition Prevention and Removal of Sulfide Scales Using Novel Chemicals." In CORROSION 2020. NACE International, 2020. https://doi.org/10.5006/c2020-14934.

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Abstract Sulfide scales, such as ZnS or FeS, are not as common as carbonate and sulfate scales, but an effective way to control them has not been fully developed. Solubility of ZnS and FeS is extremely low. As a result, it does not require a great amount of metal ions to precipitate sulfide scales. Once they are deposited on the surface, it is difficult to remove them due to their low solubility. The objectives of this study are to identify more effective and efficient chemicals for prevention and removal of sulfide scale deposits and to understand the sulfide scale control mechanism of these
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Yeoman, A. M., and A. Harris. "Development of an All Organic Ferrous Metal Corrosion Inhibitor." In CORROSION 1986. NACE International, 1986. https://doi.org/10.5006/c1986-86014.

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Abstract A new organic additive for ferrous metal corrosion has been developed, a hydroxy-phosphonic acid (HPA) with carboxylate functionality. Formulations containing this new additive have shown good performance in cooling water simulation testing from pH 8 to 9 and system calcium levels of 300 to 700 ppm as calcium carbonate. Electrochemical investigations were used to develop hypotheses regarding its mechanisms of protection. These hypotheses were used to improve the cost performance of these treatment programs.
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Reports on the topic "Phosphonic acid"

1

Wagener, Ken. Precision Morphology in Sulfonic, Phosphonic, Boronic, and Carboxylic Acid Polyolefins. Defense Technical Information Center, 2013. http://dx.doi.org/10.21236/ada606523.

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2

Holcomb, Franklin H., Michael J. Binder, William R. Taylor, J. M. Torrey, and John F. Westerman. Phosphoric Acid Fuel Cells. Defense Technical Information Center, 2000. http://dx.doi.org/10.21236/ada391823.

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3

Okae, I., A. Seya, and M. Umemoto. Acid distribution in phosphoric acid fuel cells. Office of Scientific and Technical Information (OSTI), 1996. http://dx.doi.org/10.2172/460205.

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4

Murphy, Mr Thomas F. PR-226-9315-R01 Effects of Phosphoric Acid Treatment on Fusion-Bonded Epoxy Coating Performance. Pipeline Research Council International, Inc. (PRCI), 1994. http://dx.doi.org/10.55274/r0011905.

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Abstract:
The objective of the research was to establish whether phosphoric acid treatment of line pipe should routinely be undertaken before the application of FBE coatings where chloride contamination is not present; to determine the levels of treatment which enhance or cause deterioration on the steel surface; to establish any synergism that may exist between specific FOE coatings and phosphoric acid treatment; to determine if coating performance correlates to residual phosphate on the steel surface, and to provide end-user companies with data to enable the proper selection of surface treatments for
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5

Ray, R. J. Ion Chromatography Analysis of Dibutyl Phosphoric Acid. Office of Scientific and Technical Information (OSTI), 1998. http://dx.doi.org/10.2172/4867.

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6

Unger, Robert J., Scott Kenner, Michael J. Binder, and Franklin H. Holcomb. Phosphoric Acid Fuel Cells Test and Evaluation. Defense Technical Information Center, 2004. http://dx.doi.org/10.21236/ada431752.

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7

Pierce, R. A. Progress report on nitric-phosphoric acid oxidation. Office of Scientific and Technical Information (OSTI), 1994. http://dx.doi.org/10.2172/10194991.

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8

Smith, J. R., R. A. Pierce, and E. F. Sturcken. Nitric-phosphoric acid treatment of TRU wastes. Office of Scientific and Technical Information (OSTI), 1993. http://dx.doi.org/10.2172/10116383.

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9

Author, Not Given. Advanced water-cooled phosphoric acid fuel cell development. Office of Scientific and Technical Information (OSTI), 1992. http://dx.doi.org/10.2172/7039349.

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10

Pierce, R. A. Dibutyl Phosphoric Acid Solubility in High-Acid, Uranium-Bearing Solutions at SRS. Office of Scientific and Technical Information (OSTI), 1998. http://dx.doi.org/10.2172/4886.

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