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Relevant bibliographies by topics / Imidazole Compounds

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Academic literature on the topic 'Imidazole Compounds'

Author: Grafiati

Published: 5 June 2025

Last updated: 1 August 2025

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Journal articles on the topic "Imidazole Compounds"

1

Aly, Ashraf A. "Base Catalyzed Synthesis of Novel Fused-Imidazoles from N-Vinyl-1H-imidazole." Zeitschrift für Naturforschung B 60, no. 1 (2005): 106–12. http://dx.doi.org/10.1515/znb-2005-0116.

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Syntheses of various classes of fused-imidazoles are reported. The key to their successful synthesis depends on the reaction of N-vinyl-1H-imidazole with the π-deficient compounds under basic conditions. Reaction of the target imidazole with 1,1,2,2-tetracyanoethylene and dimethyl acetylenedicarboxylate afforded pyrrolo[1,2-a]imidazoles. On the other site, reaction of the target imidazole with 2-dicyanomethyleneindane-1,3-dione, 2,3-dicyano-1,4-naphthoquinone gave indanylimidazolo- [1,2-a]azepine and imidazolo[2,1-a]phenanthridine derivatives, respectively. Under basic reaction condition, vari

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Ganguly, Swastika, Vatsal Vithlani, Anup Kesharwani, et al. "Synthesis, antibacterial and potential anti-HIV activity of some novel imidazole analogs." Acta Pharmaceutica 61, no. 2 (2011): 187–201. http://dx.doi.org/10.2478/v10007-011-0018-2.

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Synthesis, antibacterial and potential anti-HIV activity of some novel imidazole analogs A series of 1-(2-methyl-4-nitro-imidazol-1-yl)-3-arylaminopropan-2-ones (2a-e), 2-methyl-5-nitro-1-{2-[arylmethoxy] ethyl}-1H-imidazoles (5a-d), and N-(3-hydroxyphenyl)-2-(substituted imidazol-1-yl)alkanamides (8a-e) were synthesized with the aim to develop novel imidazole analogs with broad-spectrum chemotherapeutic properties. Title compounds were evaluated for their anti-HIV and antibacterial activities.

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Gerasimova, Elena L., Elena R. Gazizullina, Maria V. Borisova, et al. "Design and Antioxidant Properties of Bifunctional 2H-Imidazole-Derived Phenolic Compounds—A New Family of Effective Inhibitors for Oxidative Stress-Associated Destructive Processes." Molecules 26, no. 21 (2021): 6534. http://dx.doi.org/10.3390/molecules26216534.

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The synthesis of inhibitors for oxidative stress-associated destructive processes based on 2H-imidazole-derived phenolic compounds affording the bifunctional 2H-imidazole-derived phenolic compounds in good-to-excellent yields was reported. In particular, a series of bifunctional organic molecules of the 5-aryl-2H-imidazole family of various architectures bearing both electron-donating and electron-withdrawing substituents in the aryl fragment along with the different arrangements of the hydroxy groups in the polyphenol moiety, namely derivatives of phloroglucinol, pyrogallol, hydroxyquinol, in

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Lipson, Victoria V., Tetiana L. Pavlovska, Nataliya V. Svetlichnaya, et al. "Novel (2-amino-4-arylimidazolyl)propanoic acids and pyrrolo[1,2-c]imidazoles via the domino reactions of 2-amino-4-arylimidazoles with carbonyl and methylene active compounds." Beilstein Journal of Organic Chemistry 15 (May 6, 2019): 1032–45. http://dx.doi.org/10.3762/bjoc.15.101.

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The unexpectedly uncatalyzed reaction between 2-amino-4-arylimidazoles, aromatic aldehydes and Meldrum’s acid has selectively led to the corresponding Knoevenagel–Michael adducts containing a free amino group in the imidazole fragment. The adducts derived from Meldrum’s acid have been smoothly converted into 1,7-diaryl-3-amino-6,7-dihydro-5H-pyrrolo[1,2-c]imidazol-5-ones and 3-(2-amino-4-aryl-1H-imidazol-5-yl)-3-arylpropanoic acids. The interaction of 2-amino-4-arylimidazoles with aromatic aldehydes or isatins and acyclic methylene active compounds has led to the formation of pyrrolo[1,2-c]imi

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Demchenko, Sergii, Roman Lesyk, Oleh Yadlovskyi, et al. "Synthesis, Antibacterial and Antifungal Activity of New 3-Aryl-5H-pyrrolo[1,2-a]imidazole and 5H-Imidazo[1,2-a]azepine Quaternary Salts." Molecules 26, no. 14 (2021): 4253. http://dx.doi.org/10.3390/molecules26144253.

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A series of novel 3-aryl-5H-pyrrolo[1,2-a]imidazole and 5H-imidazo[1,2-a]azepine quaternary salts were synthesized in 58–85% yields via the reaction of 3-aryl-6, 7-dihydro-5H-pyrrolo[1,2-a]imidazoles or 3-aryl-6,7,8,9-tetrahydro-5H-imidazo[1,2-a]azepines and various alkylating reagents. All compounds were characterized by 1H NMR, 13C NMR, and LC-MS. The conducted screening studies of the in vitro antimicrobial activity of the new quaternary salts derivatives established that 15 of the 18 newly synthesized compounds show antibacterial and antifungal activity. Synthesized 3-(3,4-dichlorohenyl)-1

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Mutoh, Katsuya, Hiroki Arai, Yoichi Kobayashi, and Jiro Abe. "Photo-control of the thermal radical recombination reaction: photochromism of an azobenzene-bridged imidazole dimer." Pure and Applied Chemistry 87, no. 6 (2015): 511–23. http://dx.doi.org/10.1515/pac-2014-0910.

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AbstractAmong various kinds of photochromic compounds, bridged imidazole dimers have been known as fast photo-switch molecules. Bridged imidazole dimers have opened up various potential applications to photochromic lenses and real-time holographic displays. The optical properties of bridged imidazole dimers strongly depend on the bridging moiety to tether two imidazole rings. Therefore, the control of the bridging structure by introducing another photochromic moiety would increase the versatility of bridged imidazole dimers. In this study, we designed and synthesized a new type of the bridged

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Ashok, S. R., and M. K. Shivananda. "Synthesis and Characterization and Antifungal Screening Studies of Some Novel Imidazole Derivatives." 1 8, no. 1 (2022): 39–43. http://dx.doi.org/10.46632/jemm/8/1/7.

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Imidazole derivatives are five-mamboed heterocyclic having nitrogen, and oxygen atoms in their ring structure and exhibiting potent as well as wide range of pharmacological activities. Current investigations of imidazole derivatives have provided information that these derivatives may have applications in antimicrobial, antifungal, antiviral, as well as antidiabitic treatments. Fen bam is an imidazole derivative developed by McNeil Laboratories in the late 1970s as a novel anxiolytic drug with an at-the-time-unidentified molecular target in the brain. The imidazole ring system is present in im

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Rani, Nidhi, Praveen Kumar, Randhir Singh, Damião P. de Sousa, and Prerna Sharma. "Current and Future Prospective of a Versatile Moiety: Imidazole." Current Drug Targets 21, no. 11 (2020): 1130–55. http://dx.doi.org/10.2174/1389450121666200530203247.

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Imidazole containing compounds have been a very much explored field since ancient times. Subsequently, it constitutes a significant moiety for the new drug development. A variety of compounds having imidazole moiety have been synthesized, evaluated and marketed for the treatment of various diseases such as antifungal, antiepileptic, ACE inhibitors and so on, as shown in the figure. The search for imidazole containing compounds with more selective biological potency with low side effects continues to be an active area of research in medicinal chemistry. This review is in an effort to highlight

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Sultana, Shameem, and G. Shiva Kumar. "Synthesis, Antimicrobial and Antitubercular Activity of Novel Imidazole Carboxamides." Asian Journal of Chemistry 35, no. 5 (2023): 1276–82. http://dx.doi.org/10.14233/ajchem.2023.27823.

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A series of novel imidazole carboxamide derivatives (6a-j) were synthesized in moderate to good yields via the oxidative esterification of 1H-imidazole-4-cabaldehyde (1) with phenol (4) followed by the aminolysis of various substituted anilines (5a-j) in the presence of 1,3-bis(2,6-diisopropylphenyl)imidazol-2-ylidene (2) (IPr, 10 mol%) and TEMPO (3) in toluene. All the compounds were characterized by IR, 1H NMR, 13C NMR and mass spectral data. The synthesized compounds were assessed in vitro for their antimicrobial and antitubercular potential. Among the synthesized compounds 6a, 6f and 6g ha

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Loubidi, M., M. Lorion, A. El Hakmaoui, P. Bernard, M. Akssira, and G. Guillaumet. "One-Step Synthesis of 1H-Imidazo[1,5-a]imidazole Scaffolds and Access to their Polyheterocycles." Synthesis 51, no. 21 (2019): 3973–80. http://dx.doi.org/10.1055/s-0039-1690182.

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In this work, we continue our adventure in the chemistry of 5-5 tri-nitrogen bicycles. We disclose herein a one-step reaction to synthesize 1H-imidazo[1,5-a]imidazoles with different substituents introduced through the use of a wide range of aldehydes and isocyanides by using a Groebke–Blackburn–Bienaymé multicomponent reaction. The aim is to build a new library of 1H-imidazo[1,5-a]imidazole scaffolds. This bicycle was then modified to access new nitrogen-containing polycyclic compounds.

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Dissertations / Theses on the topic "Imidazole Compounds"

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Palamar, A. O. "Antimicrobial and antifungal activity of certain imidazole compounds." Thesis, БДМУ, 2021. http://dspace.bsmu.edu.ua:8080/xmlui/handle/123456789/18908.

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Ta, Hue Thu. "Reactions of 5-(3-alkyltriazeno)imidazole-4-carboxamide." Thesis, University of Newcastle Upon Tyne, 1990. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.315657.

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Trnka, Michael J. "Photoaffinity labeling of cytochrome P450s with imidazole-tethered benzophenone compounds /." Thesis, Connect to this title online; UW restricted, 2004. http://hdl.handle.net/1773/8516.

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Etogo, Anthony O. "Late transition metal chemistry of imidazole-based N-heterocyclic carbene ligands synthesis, characterization and luminescence /." abstract and full text PDF (free order & download UNR users only), 2006. http://0-gateway.proquest.com.innopac.library.unr.edu/openurl?url_ver=Z39.88-2004&rft_val_fmt=info:ofi/fmt:kev:mtx:dissertation&res_dat=xri:pqdiss&rft_dat=xri:pqdiss:3209961.

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Moleko, Pulleng. "The coordination and extractive chemistry of the later 3d transition metal ions with N, N'-donor imidazole-based ligands." Thesis, Nelson Mandela Metropolitan University, 2014. http://hdl.handle.net/10948/8382.

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The application of bidentate N,N'-donor ligands, such as 2,2'-biimidazole (BIIMH2) and 2,2'-pyridylimidazole (PIMH) and (1H-benzimidazol-2yl)-N-methylmethanamine (BIMAH), in the solvent extraction of base metal ions from an acidic sulfate/sulfonate medium was investigated. PIMH and BIMAH showed selectivity for Ni(II) with the only interfering ion being Cu(II) in the pH range 1.2-1.8 but BIIMH2 lacked selectivity. The extraction patterns observed were influenced by stereochemical aspects, and this agreed well with the envisaged design of nickel(II)-specific extractants through stereochemical “t

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Banerjee, Kamalendu. "Reproductive performance and cocoon charecters of Bombyx mori L. with reference to regulated feeding and treatments with methoprene and imidazole compounds." Thesis, University of North Bengal, 1998. http://hdl.handle.net/123456789/1092.

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Milde, Bianca. "(Ethynyl-)Ferrocenyl Phosphine Palladium Complexes and (Bis-)Phosphinoimidazol(e/ium) Compounds and their Application in Homogeneous Catalysis." Doctoral thesis, Universitätsbibliothek Chemnitz, 2012. http://nbn-resolving.de/urn:nbn:de:bsz:ch1-qucosa-90521.

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Die vorliegende Dissertation beschäftigt sich mit der Synthese, der Charakterisierung und der Anwendung neuartiger Phosphane in homogenkatalytischen Reaktionen. Dabei wurden die Ferrocenyl- und Ferrocenylethinylphosphan-Palladium und Ferrocenylethinylphosphan-Ruthenium Komplexe in der Palladium-vermittelten Mizoroki-Heck- und Suzuki-Miyaura-Reaktion sowie der Ruthenium-katalysierten Synthese von β-Oxopropylestern verwendet. Der Schwerpunkt lag dabei auf der Untersuchung des Einflusses der elektronischen und räumlichen Eigenschaften der Phosphanliganden auf die Aktivität und Produktivität der e

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Arrué-Muñoz, Ramón. "Magnétisme coopératif dans des composés de coordination à base de Cu(II), Ni(II) et Co(II) et ligands imidazole carboxyliques." Thesis, Rennes 1, 2014. http://www.theses.fr/2014REN1S113/document.

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La présente thèse traite de la synthèse à température ambiante et pression atmosphérique de différents composés de coordination hybrides organique-inorganiques. La partie inorganique de ces composés est constituée d’éléments de transition de la première période 3dn divalents: cobalt, nickel et cuivre. Les ligands utilisés constituent la partie organique de ces composés. Les ligands employés sont l’acide-1H-imidazol-4-carboxilique (H2IMC) et l’acide-1H-imidazol-4,5-dicarboxílique (H3IMDC). La composante inorganique Mx+ est introduite dans le composé terminal en utilisant le précurseur métalliqu

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Björk, Malin. "Synthesis of sulfur and seleniumn heterocycles, including derivatives of imidazopyridine and benzimidazole /." Stockholm, 2005. http://diss.kib.ki.se/2005/91-7140-597-6/.

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Langlet, Abraham. "Nitration of Oxo-pyramidines and Oxo-imidazoles." Doctoral thesis, KTH, Kemi, 2006. http://urn.kb.se/resolve?urn=urn:nbn:se:kth:diva-601.

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This thesis is mainly focused on the reactions of oxo-pyrimidines and oxo-imidazoles with nitric acid in sulfuric acid and properties of the gem-dinitro products formed in this process. Low temperature nitrations of 2-methylimidazoles produced – in addition to the known 2-methyl-5(4)-nitroimidazole – 2-(dinitromethylene)-5,5-dinitro-4-imidazolidinone and parabanic acid. This tetranitro compound was also obtained via nitration of 2-methyl-4,4-dihydro-(1H)-5- imidazolone. Thermal decomposition of 2-(dinitromethylene)-5,5-dinitro-4-imidazolidinone yielded 2-(dinitromethylene)-4,5-imidazolidinedio

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Books on the topic "Imidazole Compounds"

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1931-, Volodarsky Leonid B., ed. Imidazoline nitroxides. CRC Press, 1988.

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Hofmann, Klaus. Chemistry of Heterocyclic Compounds, Imidazole and Its Derivatives. Wiley & Sons, Incorporated, John, 2008.

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Preston, P. N. Chemistry of Heterocyclic Compounds, Condensed Imidazoles, 5-5 Ring Systems. Wiley & Sons, Incorporated, John, 2007.

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Gupta, Radha R., Vandana Gupta, and Mahendra Kumar. Heterocyclic Chemistry II: Five-Membered Heterocycles (Heterocyclic Chemistry). Springer, 1999.

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Book chapters on the topic "Imidazole Compounds"

1

Pardasani, R. T., and P. Pardasani. "Magnetic properties of hetero-bimetallic, Cu-Zn, imidazolate-bridged complex with glycylalanine and imidazole." In Magnetic Properties of Paramagnetic Compounds. Springer Berlin Heidelberg, 2017. http://dx.doi.org/10.1007/978-3-662-54237-8_368.

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Pardasani, R. T., and P. Pardasani. "Magnetic properties of homo-bimetallic, Cu-Cu, imidazolate-bridged complex with glycylalanine and imidazole." In Magnetic Properties of Paramagnetic Compounds. Springer Berlin Heidelberg, 2017. http://dx.doi.org/10.1007/978-3-662-54237-8_507.

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Pardasani, R. T., and P. Pardasani. "Magnetic properties of tetracyanonotrosylchromate(I) complex with imidazole." In Magnetic Properties of Paramagnetic Compounds. Springer Berlin Heidelberg, 2017. http://dx.doi.org/10.1007/978-3-662-49202-4_463.

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Pardasani, R. T., and P. Pardasani. "Magnetic properties of aqua-glycylglycinato-imidazole-copper(II)." In Magnetic Properties of Paramagnetic Compounds. Springer Berlin Heidelberg, 2017. http://dx.doi.org/10.1007/978-3-662-53974-3_455.

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Pardasani, R. T., and P. Pardasani. "Magnetic properties of copper(II) complex with imidazole." In Magnetic Properties of Paramagnetic Compounds. Springer Berlin Heidelberg, 2017. http://dx.doi.org/10.1007/978-3-662-53974-3_618.

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Pardasani, R. T., and P. Pardasani. "Magnetic properties of nitrosodicyanomethanide cobalt(II) complex with imidazole." In Magnetic Properties of Paramagnetic Compounds. Springer Berlin Heidelberg, 2017. http://dx.doi.org/10.1007/978-3-662-53971-2_404.

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Pardasani, R. T., and P. Pardasani. "Magnetic properties of imidazole-bridged tetranuclear copper(II) complex." In Magnetic Properties of Paramagnetic Compounds. Springer Berlin Heidelberg, 2017. http://dx.doi.org/10.1007/978-3-662-53974-3_365.

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Pardasani, R. T., and P. Pardasani. "Magnetic properties of copper(II) complex with imidazole derivative." In Magnetic Properties of Paramagnetic Compounds. Springer Berlin Heidelberg, 2017. http://dx.doi.org/10.1007/978-3-662-53974-3_470.

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Pardasani, R. T., and P. Pardasani. "Magnetic properties of copper(II) complex with glycylalanine and imidazole." In Magnetic Properties of Paramagnetic Compounds. Springer Berlin Heidelberg, 2017. http://dx.doi.org/10.1007/978-3-662-54237-8_22.

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Pardasani, R. T., and P. Pardasani. "Magnetic properties of copper(II) complex with glycylalanine and imidazole." In Magnetic Properties of Paramagnetic Compounds. Springer Berlin Heidelberg, 2017. http://dx.doi.org/10.1007/978-3-662-54237-8_307.

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Conference papers on the topic "Imidazole Compounds"

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Mannan, Abdul, A. C. Ferrel-Alvarez, Victor H. Ponce Valderrama, and H. Castaneda. "Interfacial Characterization of C1018 Using Ionic Liquids and Organic Imidazoline Compound." In CONFERENCE 2025. AMPP, 2025. https://doi.org/10.5006/c2025-00608.

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Abstract In the recent development of advanced chemicals used to influence the electrolyte/substrate interface; novel ILs have made subsequent progress in affecting the kinetics of the electrochemical reactions in a sustainable manner. In this research, the Imidazole-based IL [EMIM Ac] and conventional organic Imidazoline inhibitor were investigated for their effectiveness upon carbon steel alloy C1018 coupons in a 3.5 wt% NaCl environment. To study their corrosion behavior, electrochemical techniques were employed at a stationary state, maintaining 60°C with increasing inhibitor concentration

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Yang, Dongrui, Omar Rosas, and Homero Castaneda. "Comparison of the Corrosion Inhibiting Properties of Imidazole Based Ionic Liquids on API X52 Steel in Carbon Dioxide Saturated NaCl Solution." In CORROSION 2014. NACE International, 2014. https://doi.org/10.5006/c2014-4357.

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Abstract The aim of this work is to investigate the corrosion inhibiting efficiency of four imidazolium ionic liquids in carbon dioxide saturated NaCl Brine solution by using electrochemical and surface analysis testing methods. The four compounds are 1-Ethyl-3-methylimidazolium chloride (Emc), 1-Butyl-3-methylimidazolium chloride (Bmc), 1-Hexyl-3-methylimidazolium chloride (Hmc), and 1-Decyl-3-methylimidazolium chloride (Dmc). Under the testing conditions, compound Dmc showed the highest inhibition efficiency. After 24 hours of immersion time in the inhibiting solution, the inhibiting efficie

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Olivo, J. M. Domínguez, Shuyun Cao, D. Young, B. Brown, and S. Nesic. "Effect of Corrosion Inhibitor Head Group on the Electrochemical Processes Governing CO2 Corrosion." In CORROSION 2020. NACE International, 2020. https://doi.org/10.5006/c2020-14925.

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Abstract The use of corrosion inhibitors is a common practice used to mitigate internal pipeline corrosion in the oil and gas industry. An organic corrosion inhibitor is a molecule comprised of a head group (hydrophilic part) and an alkyl tail (hydrophobic part). Despite the significant amount of work associating the effect of the head group with the mode of adsorption of the inhibitor (such as bonding, effect on the tilt angle of the tail, and hysteresis), there is a lack of research relating the effect of the head group with the electrochemical processes governing the corrosion of mild steel

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Gough, M. A., W. H. Durnie, E. K. Auty, and Bill Hedges. "Characterization, Isolation and Performance Characteristics of Imidazolines." In CORROSION 2002. NACE International, 2002. https://doi.org/10.5006/c2002-02301.

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Abstract Imidazolines have been used in the area of corrosion inhibition since at least the mid 1940's when it was shown that long chain organic compounds with polar functional groups had corrosion inhibition properties when applied to oil-field environments. Many fundamental studies involving imidazoline-type compounds have been conducted and reported but although many acknowledge that conventional imidazoline contains multiple species, i.e., imidazoline, amide precursor etc., none have endeavoured to separate/isolate the various components. Therefore, the extent to which each of the componen

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Quraishi, M. A., and V. Bhardwaj. "Inhibition of Metallic Corrosion by Some 2-Cinnamyl Imidazoline Salts under Vapor Phase Conditions." In CORROSION 2003. NACE International, 2003. https://doi.org/10.5006/c2003-03365.

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Abstract Four organic volatile corrosion inhibitors (VCIs) were synthesized using 2-cinnamyl imidazoline with various acids such as salicylic acid, maleic acid, nitrobenzoic acid and phthalic acid and evaluated as corrosion inhibitors of mild steel, brass and copper by weight loss method. Eschke test method, sodium chloride inoculation test method and sulfur dioxide (SO2) test method were also carried out to investigate the corrosion inhibiting effect of the compounds. All the investigated VCIs exhibited good inhibition efficiency (IE) for all the metals. Phthalate salt showed best result amon

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Du, Min, and Bin Jiang Jing Zhang. "Study on Inhibition Behavior of Dissymmetric BIS-Quaternary Ammonium with Imidazoline Ring." In CORROSION 2010. NACE International, 2010. https://doi.org/10.5006/c2010-10150.

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Abstract Dissymmetric bis-quaternary ammonium with imidazoline ring was studied for inhibition behavior in 1.0 mol·L-1 hydrochloric acid solution at room temperature by mass loss, potentio-dynamic polarization, electrochemical impedance spectrum (EIS) and scanning electron microscopy (SEM). The result of mass loss indicated that the inhibition efficiency increased with the increase in inhibitor concentration and was over 98 % with the addition of 50 mg·L-1 inhibitor. Polarization data showed that the compound acted as a cathodic inhibitor for Q235 steel by changing the OCP to more negative val

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Wong, Jennifer E., and Neil Park. "Further Investigation on the Effect of Corrosion Inhibitor Actives on the Formation of Iron Carbonate on Carbon Steel." In CORROSION 2009. NACE International, 2009. https://doi.org/10.5006/c2009-09569.

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Abstract Many studies have been conducted on the action of corrosion inhibitors on corrosion product layers. There are varying opinions: the inhibitor may preferentially interact with the metallic surface or the existence of a corrosion scale enhances inhibitor adsorption. This paper will address the effect of the type of corrosion inhibitor active on the growth of iron carbonate. Our paper1 presented at NACExpo 2008 explored the synergistic interaction a quaternized amine compound has with iron carbonate. This work is a continuation and examines how imidazoline and phosphate ester compounds i

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Durnie, W. H., and M. A. Gough. "Characterization, Isolation and Performance Characteristics of Imidazolines. Part II. Development of Structure - Activity Relationships." In CORROSION 2003. NACE International, 2003. https://doi.org/10.5006/c2003-03336.

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Abstract Imidazolines have been used in the area of corrosion inhibition since at least the mid 1940’s when it was shown that long chain organic compounds with polar functional groups had corrosion inhibition properties when applied to oil-field environments. Part I. of this paper reported the synthesis, separation/isolation and performance characteristics of various imidazoline species synthesised from oleic acid (OA) and diethylenetriamine (DETA). These techniques have been employed in order to yield relatively ‘pure’ imidazolines for more detailed study. This paper presents the preliminary

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Menendez, Carlos M., and Zhengwei Liu. "Mechanistic Correlations between Single and Multicomponent Corrosion Inhibitor Blends for CO2 Corrosion Control." In CORROSION 2017. NACE International, 2017. https://doi.org/10.5006/c2017-09190.

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Abstract Information about the corrosion inhibition mechanism of multi-components blends and of their respective individual components is vital to identify the synergistic interactions needed to maximize performance. The mechanistic information was obtained employing such electrochemical techniques as linear polarization (LPR), electrochemical frequency modulation (EFM) and potentiodynamic polarization while using a rotating cylinder electrode (RCE) system under CO2 corrosion conditions. The employed electrochemical methods allow determination of anodic, cathodic or mixed corrosion inhibition

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Wang, Qiwei, Tao Chen, Hameed Al-Badairy, Sultan Alsubaie, Yasser Al-Jeshi, and Mohammad Alsidan. "A Further Look at the Impacts of Corrosion Inhibitor on Scale Prevention." In CONFERENCE 2022. AMPP, 2022. https://doi.org/10.5006/c2022-17676.

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Abstract In the previous work (paper C2021-16736), we presented the results on calcium carbonate deposition and inhibition in the presence of 50 ppm of corrosion inhibitors. Further studies were performed to investigate the influence of three corrosion inhibitors at high concentrations on calcium carbonate formation and the performance of scale inhibitors, to simulate the conditions where high corrosion inhibitor dosages are applied or during the early flow back stage after batch treatment. The active ingredients are, respectively, quaternary ammonium, phosphate ester and fatty acid; imidazoli

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Reports on the topic "Imidazole Compounds"

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Ramakrishnan, V. T., M. Vedachalam, and J. H. Boyer. Dense Compounds of C, H, N, and O Atoms. 2. Nitramine and Nitrosamine Derivatives of 2-Oxo- and 2-Iminooctahydroimidazo(4,5-d)Imidazole. Defense Technical Information Center, 1991. http://dx.doi.org/10.21236/ada238856.

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