Academic literature on the topic 'Anion'

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Journal articles on the topic "Anion"

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Talanov, M. V., V. B. Shirokov, and V. M. Talanov. "Anion order in perovskites: a group-theoretical analysis." Acta Crystallographica Section A Foundations and Advances 72, no. 2 (2016): 222–35. http://dx.doi.org/10.1107/s2053273315022147.

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Anion ordering in the structure of cubic perovskite has been investigated by the group-theoretical method. The possibility of the existence of 261 ordered low-symmetry structures, each with a unique space-group symmetry, is established. These results include five binary and 14 ternary anion superstructures. The 261 idealized anion-ordered perovskite structures are considered as aristotypes, giving rise to different derivatives. The structures of these derivatives are formed by tilting ofBO6octahedra, distortions caused by the cooperative Jahn–Teller effect and other physical effects. Some deri
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Wilkinson, Hazel S., and William T. A. Harrison. "Hexane-1,6-diammonium bis(dihydrogenarsenate): infinite anionic layers containing R 6 6(24) loops." Acta Crystallographica Section E Structure Reports Online 63, no. 3 (2007): m902—m904. http://dx.doi.org/10.1107/s1600536807007672.

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The title compound, C6H18N2 2+·2H2AsO4 −, contains a network of doubly protonated centrosymmetric hexane-1,6-diammonium cations and dihydrogenarsenate anions. These species interact by way of cation-to-anion N—H...O and anion-to-anion O—H...O hydrogen bonds, the latter leading to infinite sheets of the H2AsO4 − anions.
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Attiogbe, Francis K., Samar K. Bose, Wei Wang, Alastair McNeillie, and Raymond C. Francis. "The peroxymonocarbonate anions as pulp bleaching agents. Part 1. Results with lignin model compounds and chemical pulps." BioResources 5, no. 4 (2010): 2208–20. http://dx.doi.org/10.15376/biores.5.4.2208-2220.

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The peroxymonocarbonate mono-anion (HCO4─) is generated when the bicarbonate anion is added to a H2O2 solution. The mono-anion is believed to have a pKa value of ca. 10 and as such would start dissociating to the di-anion (CO42─) at pH ca. 8. The mono-anion should demonstrate electrophilic properties, while the di-anion should be a nucleophile. In an alkaline, non-sulfur pulping process such as soda/AQ, Na2CO3 could be obtained from the chemical recovery system and carbonated with CO2 from a flue gas stream to produce NaHCO3. In such a case only H2O2 would need to be purchased to generate the
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Peñas-Sanjuán, Antonio, Celeste García-Gallarín, María L. Godino-Salido, Rafael López-Garzón, Michele Melchionna, and Manuel Melguizo. "Carbon-Supported Hyperbranched Polyethyleneimines: Exploring into Polyamine/Anion Interactions to Design Efficient Polymer-Based Energy and Scavenger Materials." Polymers 17, no. 6 (2025): 786. https://doi.org/10.3390/polym17060786.

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The anion-complexation mechanism and anion-adsorption capacity of a hybrid material based on hyperbranched polyethyleneimine (HBPEI) covalently bonded onto an activated carbon (AC) is presented. The anion-scavenger behavior of this hybrid material toward CrO42−, PO43−, AsO43− and HgCl42− was explored by direct potentiometric and adsorption measurements, which revealed a novel approach to predict the interactions between the supported polymeric complexing units and the different anions. The results were analyzed by considering the reactivity data of the HBPEI/anion (HBPEI free in solution) and
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Parthé, Erwin. "Crystal chemical information to be obtained from the bond-number equality concept." Acta Crystallographica Section B Structural Science 62, no. 2 (2006): 335–37. http://dx.doi.org/10.1107/s0108768106003065.

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Based on the bond-number equality concept an equation is derived for anion complexes of normal valence compounds with triangularly and/or tetrahedrally coordinated central atoms and anions having one, two, three and four bonds to central atoms: %Δ = 4 − (n/m′) × [2 − %A [1] + %A [3] + 2 × %A [4]]. %Δ is the ratio of the number of central atoms with triangular anion coordination to the sum of all central atoms in the anion complex. n/m′ is the ratio of the number of all A anions to the number of all central atoms C′ in the anion complex. %A [1] is the ratio of the number of anions with one bond
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Sun, Jing, Qing Shan Li, Wei Hong, Biao Zhan, Guo Wei Wang, and Guang Zhong Xing. "The Two-Step Process for the Production of Anion Acrylic Fiber." Applied Mechanics and Materials 320 (May 2013): 615–18. http://dx.doi.org/10.4028/www.scientific.net/amm.320.615.

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This article describes the preparation process of the anion acrylic and its test. In this study, using natural mineral nanomaterials prepared anion additives, using a two-step prepared anion acrylic fiber. Has been tested, the anion acrylic the indicators are good, the anion release can reach 1430 anions / cm3, and can be widely used in clothing, textile, medical and other fields.
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Schefe, C. R., M. Watt, W. J. Slattery, and P. M. Mele. "Organic anions in the rhizosphere of Al-tolerant and Al-sensitive wheat lines grown in an acid soil in controlled and field environments." Soil Research 46, no. 3 (2008): 257. http://dx.doi.org/10.1071/sr07139.

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Several sampling methods were investigated for the quantification of organic anions in the rhizosphere of Al-tolerant (ET8) and Al-sensitive (ES8) wheat plants in soil systems. Controlled environment studies used anion exchange membranes to collect rhizosphere organic anions (from root tips and mature regions of nodal roots) from ET8 and ES8 plants at the 6-leaf stage in a glasshouse environment. Using the anion exchange membranes, a selection of organic anions were detected on the tips and mature regions of roots, with ET8 and ES8 having similar rhizosphere organic anion profiles. The field e
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Wilkinson, Hazel S., and William T. A. Harrison. "2-Methylpiperazinium bis(dihydrogenarsenate)." Acta Crystallographica Section E Structure Reports Online 63, no. 3 (2007): m900—m901. http://dx.doi.org/10.1107/s1600536807008392.

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The title compound, C5H14N2 2+·2H2AsO4 −, contains a network of centrosymmetric doubly protonated 2-methylpiperazinium cations, showing disorder of the methyl group, accompanied by dihydogenarsenate anions. The component species interact by way of cation-to-anion N—H...O and anion-to-anion O—H...O hydrogen bonds, the latter leading to infinite sheets of the H2AsO4 − anions containing R 6 6(24) supramolecular loops.
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Cervera, Maria, and Jordi Marquet. "Effects of superoxide anion generated from aromatic radical anions produced in nucleophilic aromatic photosubstitution reactions." Canadian Journal of Chemistry 76, no. 6 (1998): 966–69. http://dx.doi.org/10.1139/v98-044.

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Superoxide anion is generated from aromatic radical anions produced in nucleophilic aromatic photosubstitutions when the reactions are carried out in non-deoxygenated solutions of polar aprotic solvents. Superoxide anion thus generated displaces cyanide anion from acetonitrile and benzyl cyanide, ethoxide anion from ethyl acetate, and methanesulfenate anion from dimethyl sulfoxide. Hence, non-deoxygenated polar aprotic solvents should be avoided in nucleophilic aromatic photosubstitution reactions.Key words: superoxide, fluoride, nucleophilic aromatic photosubstitution.
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Li, Lei, Yu-Jian Hong, Dong-Yang Chen, Wang-Chuan Xiao та Mei-Jin Lin. "Anion–π interactions in lithium–organic redox flow batteries". Chemical Communications 55, № 16 (2019): 2364–67. http://dx.doi.org/10.1039/c8cc09834d.

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The interactions between the electrolyte anions and electron-deficient redox-active organic molecules (anion–π interactions) have strong influences on the battery properties due to the anion–π-induced formation of radical anions or sandwich-like aggregates.
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Dissertations / Theses on the topic "Anion"

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Drumright, Ray E. "Radical anion rearrangements. aryl cyclopropyl ketyl anions." Diss., This resource online, 1991. http://scholar.lib.vt.edu/theses/available/etd-07282008-134853/.

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Sun, Zhanhu [Verfasser]. "Quinoline-based anion receptors and anion-pi interactions / Zhanhu Sun." Aachen : Hochschulbibliothek der Rheinisch-Westfälischen Technischen Hochschule Aachen, 2013. http://d-nb.info/1042551367/34.

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Wang, Zhiming 1958. "Anion Exchange and Competition in Layered Double Hydroxides." Thesis, University of North Texas, 1997. https://digital.library.unt.edu/ark:/67531/metadc332481/.

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Exchange reactions of anions, especially ferrocyanide and carbonate, with layered double hydroxides (LDHs) were investigated in relation to the origin of life on the early Earth. The effect on ferrocyanide exchange of concentration, pH, reaction time and cations are discussed. It was found that there were two different kinds of ferrocyanide species: one was that intercalated into the layered structure, occupying a site of D symmetry within the LDHs, while in the other, the ferrocyanide group retains full O symmetry. In addition, very low concentration, ferrocyanide associated with LDH will cha
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Andrews, Django H. "Anion photoelectron spectroscopy." Diss., Connect to online resource, 2006. http://gateway.proquest.com/openurl?url_ver=Z39.88-2004&rft_val_fmt=info:ofi/fmt:kev:mtx:dissertation&res_dat=xri:pqdiss&rft_dat=xri:pqdiss:3239380.

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Wietek, Jonas. "Anion Conducting Channelrhodopsins." Doctoral thesis, Humboldt-Universität zu Berlin, 2018. http://dx.doi.org/10.18452/19325.

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Seit mehr als 10 Jahren kann biologische Aktivität durch eine Vielzahl photosensorischer Proteine beeinflusst werden. In diesem als Optogenetik bezeichneten Forschungsgebiet, werden Kationen leitende Kanalrhodopsine (CCRs) als lichtinduzierte neuronale Aktivatoren eingesetzt. Diese Arbeit soll zur Vervollständigung von optogenetischen Werkzeugen durch die Entwicklung Anionen leitender Kanalrhodopsine (ACRs) dienen, um die bestehenden Nachteile mikrobieller lichtgetriebener Ionenpumpen zu überwinden, die bislang zur neuronale Inhibition genutzt wurden. Der Austausch von E90 in C. reinhardtii K
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Calin, Nathalie. "Etude thermique de quelques sels d'hétéropolymolybdates : mise en évidence d'interactions anion-anion et anion-cation à l'état solide." Lille 1, 2001. https://pepite-depot.univ-lille.fr/LIBRE/Th_Num/2001/50376-2001-119.pdf.

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Les polyoxométallates et plus particulièrement les hétéropolymolybdates sont des composés très recherchés en catalyse, homogène ou hétérogène. A l'état solide, leur comportement réactif dépend de nombreux paramètres dont la nature des contre-ions présents, le type de molécules de solvatation, le système cristallin et leur evolution thermique. Plusieurs sels (sodium, potassium, alkyl(aryl)ammonium) des ions dodécamolybdophosphate (3-), vanadoundécamolybdophosphate (4-) et de structures apparentées (octadécamolybdophosphate (6-)) ont été préparés. Ils ont été étudiés en solution par polarographi
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Ferguson, Richard. "Fluorescent Anion Sensing and Anion Templated Assembly of Interpenetrated Molecular Architectures." Thesis, University of Oxford, 2008. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.491446.

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The main aim: of this project is to develop novel acyclic and macrocyclic hosts for the binding and fluorescent sensing of anionic guests in solution. In addition the use of these hosts in anion templated interpenetrated architectures was exploited. Chapter One introduces the field of supramolecular chemistry and gives a brief description of the non-covalent forces employed in supramolecular host design. A description of the areas of anion binding and the more sophisticated discipline of anion sensing is given. The Chapter concludes with a discussion of the phenomenon of selfassembly and in pa
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Sekizaki, Shuichi. "Development of conducting cation radical salts with flexible organic anions : tetracyanoallyl anion derivatives." 京都大学 (Kyoto University), 2006. http://hdl.handle.net/2433/144214.

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Zain, S. A. M. "Novel inorganic anion exchangers." Thesis, University of Salford, 1988. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.234769.

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Swinburne, Adam Neil. "Induced-fit anion sensing." Thesis, Durham University, 2011. http://etheses.dur.ac.uk/579/.

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Anions have many important roles in biological systems, as well as in the environment and as such there is significant interest in their binding and sensing. In induced-fit anion sensing, the binding of an anion causes a shift in the equilibrium of conformers of the molecule, which in turn may lead to a change in a physical property. In this thesis four experimental chapters describe the synthesis and anion sensing properties of a series of induced-fit anion sensors derived from a hexa-substituted triethylbenzene and diphenylacetylene motif. Chapter one provides an introduction to anion recogn
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Books on the topic "Anion"

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Stibor, Ivan, ed. Anion Sensing. Springer Berlin Heidelberg, 2005. http://dx.doi.org/10.1007/b101055.

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Stoddart, J. Fraser, ed. Anion Receptor Chemistry. Royal Society of Chemistry, 2007. http://dx.doi.org/10.1039/9781847552471.

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Bowman-James, Kristin, Antonio Bianchi, and Enrique García-España, eds. Anion Coordination Chemistry. Wiley-VCH Verlag GmbH & Co. KGaA, 2011. http://dx.doi.org/10.1002/9783527639502.

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A, Gale Philip, and Cho Won-Seob, eds. Anion receptor chemistry. Royal Society of Chemistry, 2006.

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Gale, Philip A., W. Dehaen, and E. Alcade. Anion recognition in supramolecular chemistry. Springer, 2010.

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Krueger, James Harry. Cation and anion chemistry. O.S.U. Book Stores, 1986.

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Syed Abdul Malik Bin Syed Zain. Novel inorganic anion exchangers. University of Salford, 1988.

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Fahlke, Christoph, ed. Anion Channels and Transporters. Springer International Publishing, 2024. http://dx.doi.org/10.1007/978-3-031-51346-6.

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Gale, Philip A., and Wim Dehaen, eds. Anion Recognition in Supramolecular Chemistry. Springer Berlin Heidelberg, 2010. http://dx.doi.org/10.1007/978-3-642-15444-7.

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An, Liang, and T. S. Zhao, eds. Anion Exchange Membrane Fuel Cells. Springer International Publishing, 2018. http://dx.doi.org/10.1007/978-3-319-71371-7.

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Book chapters on the topic "Anion"

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Bährle-Rapp, Marina. "Anion." In Springer Lexikon Kosmetik und Körperpflege. Springer Berlin Heidelberg, 2007. http://dx.doi.org/10.1007/978-3-540-71095-0_653.

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Charnley, Steven B. "Anion." In Encyclopedia of Astrobiology. Springer Berlin Heidelberg, 2014. http://dx.doi.org/10.1007/978-3-642-27833-4_80-5.

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Charnley, Steven B. "Anion." In Encyclopedia of Astrobiology. Springer Berlin Heidelberg, 2015. http://dx.doi.org/10.1007/978-3-662-44185-5_80.

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Böning, Dieter, Michael I. Lindinger, Damian M. Bailey, et al. "Anion." In Encyclopedia of Exercise Medicine in Health and Disease. Springer Berlin Heidelberg, 2012. http://dx.doi.org/10.1007/978-3-540-29807-6_2094.

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Charnley, Steven B. "Anion." In Encyclopedia of Astrobiology. Springer Berlin Heidelberg, 2023. http://dx.doi.org/10.1007/978-3-662-65093-6_80.

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Gooch, Jan W. "Anion." In Encyclopedic Dictionary of Polymers. Springer New York, 2011. http://dx.doi.org/10.1007/978-1-4419-6247-8_661.

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Gooch, Jan W. "Anion." In Encyclopedic Dictionary of Polymers. Springer New York, 2011. http://dx.doi.org/10.1007/978-1-4419-6247-8_13127.

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Gale, Philip A., and Claudia Caltagirone. "Anion Sensors." In Chemosensors. John Wiley & Sons, Inc., 2011. http://dx.doi.org/10.1002/9781118019580.ch19.

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Agúndez, Marcelino. "C3N− Anion." In Encyclopedia of Astrobiology. Springer Berlin Heidelberg, 2023. http://dx.doi.org/10.1007/978-3-662-65093-6_5517.

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Marcelino, Agúndez. "C5N− Anion." In Encyclopedia of Astrobiology. Springer Berlin Heidelberg, 2023. http://dx.doi.org/10.1007/978-3-662-65093-6_5518.

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Conference papers on the topic "Anion"

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McIntyre, J. F., and T. S. Dow. ""Intergranular Corrosion Behavior of Aluminum Alloys Exposed to Artificial Seawater in the Presence of Nitrate Anion"." In CORROSION 1991. NACE International, 1991. https://doi.org/10.5006/c1991-91501.

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Abstract Research was conducted to better understand the nature of a synergistic attack of 7XXX aluminum alloys exposed to artificial seawater and nitrate anions. In the presence of nitrate anion, intergranular corrosion of these alloys was accelerated. The importance of grain boundary microstructure and chemical composition on intergranular corrosion is discussed with respect to intermetallic reactivity and connectivity.
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Murray, John N. "Activation of the Al-Zn-In Anode; Effects of the Test Solution Composition." In CORROSION 2006. NACE International, 2006. https://doi.org/10.5006/c2006-06682.

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Abstract The majority of investigations of Al-Zn-In sacrificial anode alloys has involved determining the electrochemical behavior in natural or substitute ocean water. Several investigators have noted that the activation process “needs” chloride ion (Cl-) and there are at least two publications suggesting the sulfate (SO4=) anion inhibits aluminum corrosion and/or indium activated alloy capability. Therefore, activation testing was conducted with a variety of anions including mixed chloride/sulfate solutions of various combinations and concentrations. The results are presented and discussed.
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Yomura, Y., and T. Adaniya. "Electrodeposited Chromate Films on Coated Steel Sheets." In CORROSION 1988. NACE International, 1988. https://doi.org/10.5006/c1988-88177.

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Abstract Ion permeability of electrodeposied chromate film was investigated in an attempt to develop an effective coating system for corrosion protection. The occurence of selective permeability was successfully demonstrated by measuring membrane potential. Although as-electrodeposited chromate film was an anion-selective film (i.e. anions permeate preferencially), "oxoacid-treated" chormate films were cation-selective films (i.e. cations permeate preferencially). A double-layered chromate coating which consisted of as-electrodeposited layer and oxoacid-treated layer performed well for contain
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Ghanbari, Elmira, Alireza Saatchi, Danyil Kovalov, Bruno Kursten, and Digby D. Macdonald. "The Influence of Halide Ions on the Passivity Breakdown of Carbon Steel Based on the Point Defect Model." In CORROSION 2018. NACE International, 2018. https://doi.org/10.5006/c2018-11025.

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Abstract An important factor in determining the breakdown of the barrier layer of the passive film on carbon steel in halide-containing solutions is the anion size. In this study, the influence of the size of aggressive anions on the passivity breakdown of UNS K02700 grade carbon steel exposed to saturated Ca(OH)2 solutions with the addition of different halides was investigated by using the potentiodynamic polarization (PDP) experiments. The PDP results were interpreted by using a mechanistic description based on the Point Defect Model (PDM). The experimental results revealed a linear depende
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Ciaraldi, S. W. "Some Limitations on the Use of 13Cr Alloys for Corrosive Gas and Oil Production." In CORROSION 1990. NACE International, 1990. https://doi.org/10.5006/c1990-90071.

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Abstract Laboratory investigations and field experience continue to define the application limits of 13Cr alloys. Recent stress corrosion cracking tests have developed a direct relationship between tolerable H2S levels and acetate anion contents of test brines. Strength level was found to be an important variable in the chloride-induced cracking of nickel containing alloys. Corrosion related service failures have been attributed to organic acid levels of produced fluids and flow related effects. Laboratory tests have demonstrated acetate anions to significantly influence corrosion behavior. A
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Cummings, Arthur L., Fred C. Veatch, and Alfred E. Keller. "Corrosion and Corrosion Control Methods in Amine Systems Containing H2S." In CORROSION 1997. NACE International, 1997. https://doi.org/10.5006/c1997-97341.

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Abstract Overall H2S-amine system corrosion rates are determined by the rate of acid oxidation of iron by dissolved forms of H2S and CO2 in highly buffered basic solutions. Rates of interference with the laydown or removal of the protective layer of iron sulfide corrosion product from the free metal are also part of the equation. These two phenomena are functions of the concentration and form of the oxidizing acid, the solution temperature, the fluid velocity, and the concentration of heat stable salt anions. The effect of solution pH, cation content and different heat stable salt anions on th
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Andrew, B. E. "Monitoring of Microbiological Metabolites by Ion Chromatography." In CORROSION 1988. NACE International, 1988. https://doi.org/10.5006/c1988-88089.

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Abstract Ion chromatography is a useful analytical technique for obtaining quantitative data with respect to microbiological metabolites on surfaces and in bulk solution. Case histories include anaerobic degradation of nitrite in bulk solution and on steel surfaces, resulting in microbiologically induced corrosion. Aerobic degradation of nitrite in a cooling water system will illustrate the importance of selecting appropriate simulation conditions. Short-chain fatty acids in emulsion coolants are generated by microbiological action, and can contribute to product corrosion. These metabolites ar
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Varjonen, O. A., and T. J. Hakkarainen. "Corrosion Behaviour of Titanium (Grade 5) in Alkaline Hydrogen Peroxide Bleaching Solution - Laboratory Experiments." In CORROSION 1994. NACE International, 1994. https://doi.org/10.5006/c1994-94425.

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Abstract General corrosion occurred when titanium (Grade 5) was exposed to hot alkaline hydrogen peroxide solutions (9<pH<11, CH2O2 = 2000 - 3500 mg/l). The uniform corrosion was fairly rapid and it has been verified by electrochemical and weight loss measurements. Both measurements showed comparable results. The uniform corrosion behaviour of titanium appeared to depend on both the high pH-value and on the concentration of hydrogen peroxide in the solutions. A critical pH-value for titanium can be determined when the hydrogen peroxide concentration is kept at a constant level. T
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AMINUDDIN, Muhammad Syahir. "Monocationic and dicationic phosphonium based ionic liquids: Synthesis and properties." In Decarbonization Technology: ICDT2024. Materials Research Forum LLC, 2025. https://doi.org/10.21741/9781644903575-1.

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Abstract. In the current work, two monocationic ionic liquids (MILs) and two dicationic ionic liquids (DILs) with similar trihexyl(tetradecyl)phosphonium cation, [P66614]+ and different metal chloride anions such as trichlorostannate anion, [SnCl3]-, pentachlorozirconate anion, [ZrCl5]-, tetrachloronickelate(II) anion, [NiCl4]2- and tetrachlorocuprate(II) anion, [CuCl4]2- were successfully synthesized and characterized, respectively. The structures of ILs were confirmed using FT-IR spectroscopy and CHNS elemental analysis. The effect of temperature and anion type on thermophysical properties s
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Alves, Adrielly, and Régis Casimiro Leal. "Theoretical study of the mechanism of chromogenic chemodosimeters in the detection of sulfhydryl (SH–) and hydroxyl (OH–) anions." In VIII Simpósio de Estrutura Eletrônica e Dinâmica Molecular. Universidade de Brasília, 2020. http://dx.doi.org/10.21826/viiiseedmol2020128.

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Sulfide (S2−) is a biologically and environmentally important anion. Exposure to the sulfide anion can cause chronic, respiratory diseases and irritations in the skin and mucous membranes. The protonated HS− or H2S forms are more toxic than the S2− itself. A derivative of the family of 2,4,6-triaryl-pyrylium cations bearing an amine in the para position of the 4-aryl group is sensitive for detecting sulfide anions in solution. Through DFT calculations, performed at level B3LYP/6-31+G(d) in gas phase, these authors present the thermodynamic stability of the interaction of chemodosimeters derive
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Reports on the topic "Anion"

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Shukla, Manoj K., Luidmyla K. Sviatenko, Sergly I. Okovytyy, Danuta Leszczynska, and Jerzy Leszczynski. Catalytic Role of Solvated Electron in the Spontaneous Degradation of Insensitive Munition Compounds : Computational Chemistry Investigation. Engineer Research and Development Center (U.S.), 2021. http://dx.doi.org/10.21079/11681/41122.

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The DNAN (2,4-dinitroanisole), NTO (3-nitro-1,2,4-triazol-5-one), and NQ (nitroguanidine) are important insensitive energetic materials used in military applications. They may find their way to the environment during manufacturing, transportation, storage, training, and disposal. A detailed investigation of possible mechanisms for self-degradation of radical-anions formed by addition of solvated electron to DNAN, NTO, and NQ species was performed by computational study using the PCM(Pauling)/M06-2X/6-311++G(d,p) approach. Obtained results suggest that only NQ radical-anion is able for self-deg
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Jonathan L. Sessler. Supramolecular Chemistry of Selective Anion Recognition for Anions of Environmental Relevance. Office of Scientific and Technical Information (OSTI), 2007. http://dx.doi.org/10.2172/891664.

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Moyer, Bruce a., Debra A. Bostick, Christopher J. Fowler, et al. Supramolecular Chemistry of Selective Anion Recognition for Anions of Environmental Relevance. Office of Scientific and Technical Information (OSTI), 2005. http://dx.doi.org/10.2172/893098.

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Bowman-James, Kristin, George S. Wilson, and Bruce Moyer. Supramolecular Chemistry of Selective Anion Recognition for Anions of Environmental Relevance. Office of Scientific and Technical Information (OSTI), 2001. http://dx.doi.org/10.2172/834750.

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Bowman-James, Kristin, George S. Wilson, and Bruce Moyer. Supramolecular Chemistry of Selective Anion Recognition for Anions of Environmental Relevance. Office of Scientific and Technical Information (OSTI), 2002. http://dx.doi.org/10.2172/834752.

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Bowman-James, Kristin, and George S. Wilson. Supramolecular Chemistry of Selective Anion Recognition for Anions of Environmental Relevance. Office of Scientific and Technical Information (OSTI), 2003. http://dx.doi.org/10.2172/834754.

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Bowman-James, K., G. Wilson, and B. A. Moyer. Supramolecular Chemistry of Selective Anion Recognition for Anions of Environmental Relevance. Office of Scientific and Technical Information (OSTI), 2004. http://dx.doi.org/10.2172/835027.

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Bowman-James, Kristin, and Bruce A. Moyer. Supramolecular Chemistry of Selective Anion Recognition for Anions of Environmental Relevance. Office of Scientific and Technical Information (OSTI), 2004. http://dx.doi.org/10.2172/838638.

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Bowman-James, Kristen. Supramolecular Chemistry of Selective Anion Recognition for Anions of Environmental Relevance. Office of Scientific and Technical Information (OSTI), 2004. http://dx.doi.org/10.2172/850320.

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Sessler, Jonathan L. The Supramolecular Chemistry of Selective Anion Recognition for Anions of Environmental Relevance. Office of Scientific and Technical Information (OSTI), 2005. http://dx.doi.org/10.2172/884859.

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