Academic literature on the topic 'Anilincs'

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Journal articles on the topic "Anilincs"

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M., Karthikeyan, Ghammami S., S. Bhuvam shwari D., and P. Elango K. "Preferential solvation effect on the kinetics of oxidation of parasubstituted anilines by tetramethylammonium fluorochromate." Journal of Indian Chemical Society Vol. 84, April 2007 (2007): 359–64. https://doi.org/10.5281/zenodo.5817057.

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Department of Chemistry, Gandhigram Rural University, Gandhigram-624 302, Tamilnadu, India <em>E-mail</em>: drkpelango@rediffmail.com Department of Chemistry, Faculty of Science, Imam Khomeini International University, Ghazvin. Iran <em>Manuscript received 11 December 2006, accepted 14 February 2007</em> Tetramethylammonium fluorochromate (TMAFC) oxidation of <em>para</em>-substituted aniline. in varying mole fractions of benzene in 2-methylpropan-2-ol, in the presence of <em>p</em>-toluenesulfonic acid (PTS) i.&nbsp;first-order in TMAFC and PTS and is zero-order with respect to substrate. The
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Kumbhare, Nayan, and Varsha Dhurvey. "Studies of Aniline and it’s Derivatives on Various Organ Systems: A Mini Review." International Journal of Scientific Research in Biological Sciences 12, no. 2 (2025): 21–31. https://doi.org/10.26438/ijsrbs.v12i2.672.

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Certain chemical pollutants in the environment can change a variety of biological processes. Anilines are widely used in the manufacturing of plants, colours, medications, pesticides, and herbicides. This review aims to highlight the destructive, dangerous and altering effects of aniline on various organisms. We believe that this study will provide helpful information regarding aniline's toxicological research, which will help in the formulation of acceptable guidelines for aniline usage.
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Shteinberg, Leon. "INFLUENCE OF SUBSTITUTES ON THE RATE OF THE REACTION OF ORTHOSUBSTITUTED BENZOIC ACIDS WTH ANILINE, CATALYZED BY POLYBUTOXYTITANATES." Ukrainian Chemistry Journal 87, no. 3 (2021): 18–40. http://dx.doi.org/10.33609/2708-129x.87.03.2021.18-40.

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The polybutoxytitanates catalysis of aniline acylation by orthosubstituted benzoic acids leads to the production of substituted benzanilides. Catalytic rate constants of the second order reaction (the first with respect to aniline and ortho-substituted benzoic acid; boiling ortho=xylene, 145°C) correlate well according to the Hammett and Bronsted equations with straight line segments with ρ=1.93 and α=0.66, in contrast to the reaction of aniline with meta- and parasubstituted benzoic acids and substituted anilines with benzoic acid. This dependence drops out 2=nitrobenzoic and 1=naphthoic acid
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Lewis, Frederick D., Jill M. Wagner-Brennan, and Alan M. Miller. "Article." Canadian Journal of Chemistry 77, no. 5-6 (1999): 595–604. http://dx.doi.org/10.1139/v98-229.

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The photophysical and photochemical behavior of several aniline spacer - styrene molecules in which the spacer is a short polymethylene chain has been investigated. Long wavelength excitation selectively excites the aniline chromophore which undergoes intramolecular quenching by the styrene to yield an intramolecular exciplex. Exciplex fluorescence is observed for both of the tertiary anilines investigated and for one of the three secondary anilines. More rapid exciplex formation in nonpolar vs. polar solvents is attributed to the necessity of desolvating the polar aniline singlet in polar sol
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Gorokhov, Valery Yu, and Tatiana V. Makhova. "Para-(aza,thio)xanthenylated anilines in the pereaminination reaction." Butlerov Communications 60, no. 10 (2019): 32–35. http://dx.doi.org/10.37952/roi-jbc-01/19-60-10-32.

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It is known that the biochemical enzymatic reaction of the reversible transfer of an amino group from an amino-acid to a keto-acid is called a transamination reaction. However, the transamination reaction is applicable not only for biochemical enzymatic reactions, but is also often used in organic synthesis to produce aromatic azomethines. As objects of study in the transamination reaction, we selected substituted N-benzylidenanilines (imines, Schiff bases) and anilines, containing a biologically active heterocyclic fragment in the para-position of the aniline ring. We have shown the feasibili
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Crampton, Michael R., Lynsey C. Rabbitt, and François Terrier. "Electrophilic aromatic substitution in substituted anilines; kinetics of the reaction with 4,6-dinitrobenzofuroxan." Canadian Journal of Chemistry 77, no. 5-6 (1999): 639–46. http://dx.doi.org/10.1139/v99-033.

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Kinetic results are reported for reaction of aniline and six of its N- and ring-substituted derivatives with 4,6-dinitrobenzofuroxan (DNBF) in water - dimethyl sulfoxide mixtures. In acidic solution σ-adducts, the result of electrophilic substitution in the anilines, are formed with bonding between a ring-carbon atom of the anilines and the 7-position of DNBF. Reaction normally occurs at the 4-position of the aniline unless this carries a substituent, when reaction occurs at the 2-position. A value of 2.0 for kH/kD, the kinetic isotope effect, indicates that in the reaction with aniline bond f
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Kon, Yoshihiro, Shota Tsurumi, Shunsuke Yamada, Toshiyuki Yokoi, and Tadahiro Fujitani. "Selective monoallylation of anilines to N-allyl anilines using reusable zirconium dioxide supported tungsten oxide solid catalyst." RSC Advances 12, no. 19 (2022): 11877–84. http://dx.doi.org/10.1039/d2ra00198e.

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We present a 10 wt% WO3/ZrO2 catalyzed monoallylation reaction of anilines to give various N-allyl anilines in good yields. The developed catalytic reaction is applicable to the continuous flow synthesis of N-allyl aniline with 97% selectivity.
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Hurtova, Martina, Daniela Brdová, Bára Křížkovská, et al. "Nitrogen-Containing Flavonoids-Preparation and Biological Activity." Acs Omega 9, no. 32 (2024): 34938–50. https://doi.org/10.1021/acsomega.4c04627.

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In this work, we report the application of Buchwald-Hartwig amination for the preparation of new derivatives of quercetin and luteolin. Our investigation delves into the impact of aniline moiety on antioxidant, and anti-inflammatory activity, cytotoxicity, and the ability of flavonoids to modulate drug-resistance mechanisms in bacteria. The anti-inflammatory activity disappeared after the introduction of aniline into the flavonoids and the cytotoxicity remained low. Although the ability of quercetin and luteolin to modulate bacterial resistance to antibiotics has already been published, this i
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Mieriņa, Inese, Darja Kostjuņina, Dārta Zelma Skrastiņa, and Mara Jure. "Synthesis and Antiradical Activity of 2-Arylidenemalonic Acid Dianilides." Key Engineering Materials 850 (June 2020): 230–35. http://dx.doi.org/10.4028/www.scientific.net/kem.850.230.

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The most common cinnamoyl anilines are avenanthramides, which are natural antioxidants found in oats. This is a rather uncommon and not well-investigated group of antioxidants. This paper deals with 2-arylidenemalonic acid dianilides – cinnamoyl anilines which are decorated with an additional arylaminocarbonyl moiety at α-position of double bond. The DPPH scavenging activity of the title compounds is slightly lower in comparison to the corresponding cinnamoyl anilines. On the other hand, the title dianilides are more active than cinnamic acid anilides containing an additional carboxylic group
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Wiberg, Kenneth B. "Substituent Effects on the Acidity of Weak Acids. 4. Anilinium Ions." Collection of Czechoslovak Chemical Communications 69, no. 12 (2004): 2183–92. http://dx.doi.org/10.1135/cccc20042183.

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The gas phase acidity of anilinium ions has been calculated at a number of theoretical levels from B3LYP/6-311++G** to MP2 and CCSD/6-311++G(2dp,2pd). The highest level calculations find anilinium ion and p-protonated aniline to have essentially the same energy, in agreement with experimental studies. They also give a proton affinity for aniline that is in very good agreement with the experimental value. The B3LYP and MP2 calculations are less successful, with B3LYP favoring p-protonation and MP2 favoring N-protonation for aniline. Despite this difficulty, the calculated effect of substituents
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Dissertations / Theses on the topic "Anilincs"

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Xie, Xiaoman [Verfasser]. "Anaerobic degradation of phenol and aniline by the sulfate-reducing bacterium Desulfatiglans anilini / Xiaoman Xie." Konstanz : KOPS Universität Konstanz, 2019. http://d-nb.info/123320338X/34.

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Santos, Isabela Ferreira Sodré dos. "Investigação da correlação morfologia/estrutura nos produtos da polimerização da anilina com persulfato de amônio." Universidade de São Paulo, 2013. http://www.teses.usp.br/teses/disponiveis/46/46136/tde-22102013-104923/.

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É verificado que materiais nano/micro estruturado, com morfologia definida possui propriedades melhoradas em relação às formas macro. Essa constatação justifica o crescente número de rotas diferentes para se sintetizar polianilina numa ampla gama de morfologias diferentes e tamanhos definidos, através de variações na síntese padrão de polianilina. Utilizando uma dessas rotas que leva a produto com morfologia esférica, em estudo anterior do nosso grupo foi mostrado que o produto principal é adutos de anilinas constituídos por adutos tipo 1,4-Michael entre anilina e benzoquinona monoimina e segm
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Jbarah, Abdel Aziz. "Spectroelectrochemistry of Substituted Anilines." Doctoral thesis, Universitätsbibliothek Chemnitz, 2006. http://nbn-resolving.de/urn:nbn:de:swb:ch1-200601985.

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Die Elektrochemie und die Spektroelektrochemie von Nitroanilinen (ortho-, meta- und para- Isomere) und deren entsprechenden Diaminoverbindungen (ortho-, meta- und para-Phenylendiamin) wurden an zwei verschiedenen Elektroden (Platin und Gold) und in zwei Elektrolytlösungen (saure und neutrale Perchloratlösung) untersucht. Die erhaltenen Messergebnisse wurden als Referenz für die spektroelektrochemische Untersuchung von Polyvinylaminen mit o- oder p- Nitroanilinsubstituenten verwendet. Es wurden außerdem spektroelektrochemische Untersuchungen mit anderen Polyvinylaminen, die das Wurster Kationra
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Martendal, Adriano. "Ciclização intramolecular de 2-(w-Bromoalquiloxi) anilinas /." Florianópolis, SC, 1999. http://repositorio.ufsc.br/xmlui/handle/123456789/81026.

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Dissertação (Mestrado) - Universidade Federal de Santa Catarina, Centro de Ciências Físicas e Matemáticas.<br>Made available in DSpace on 2012-10-18T21:59:36Z (GMT). No. of bitstreams: 0Bitstream added on 2016-01-09T04:30:12Z : No. of bitstreams: 1 161180.pdf: 3717444 bytes, checksum: a542739122a1b4e91024f9a09b9542ec (MD5)<br>Ciclizações intramoleculares podem ser estudadas como modelos miméticos de catálise enzimática. Esses modelos fundamentam-se no princípio de que os parâmetros físico-químicos que governam a reatividade entre dois grupamentos funcionais em uma reação intramolecular, esteja
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Fedotova, Alena. "Amines aromatiques stériquement encombrées dans la réaction d'aza-Michael : effets de solvant et haute pression." Thesis, Normandie, 2018. http://www.theses.fr/2018NORMR056/document.

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Au cours de cette thèse, nous avons rapporté que la combinaison unique de l'hexafluoroisopropanol (HFIP), utilisé comme solvant, et des conditions hyperbares (10-15 kbar) permet une addition sans précédent de nucléophiles-1,4 pauvres, comme les amines aromatiques, sur des récepteurs Michael encombrés, sans promoteur externe. De plus, l'addition d'hétéro-Michael d'anilines fonctionnellement substituées sur des esters insaturés-α,β est définie par la différence d'acidité entre le solvant et l'amine. La réaction avec des anilines plus basiques se déroule facilement dans le méthanol. En revanche,
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Zahrtmann, Nanette. "Pd-catalysed Carbonylations of Anilines in Ionic Liquid." Doctoral thesis, Universitat Rovira i Virgili, 2017. http://hdl.handle.net/10803/450855.

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Aquesta tesi descriu l'estudi de diversos catalitzadors de pal·ladi amb lligands donants de fòsfor i nitrogen disponibles al mercat, ja sigui com l'únic lligant o en combinació amb carbens N-heterocíclics. Els sistemes de pal·ladi es van aplicar en carbonilació de anilines per a la formació d'amides i urees. La tesi es divideix en quatre capítols. El primer capítol és una breu introducció a la chemisty carbonilació de catalitzadors de pal·ladi homogenis. També es discuteix reaccions de carbonilació impliquen líquids iònics i catalitzadors SILP. El segon capítol tracta de la formació d'amid
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Allott, Philip Hugh. "The thermochemistry of bromination of phenols and anilines." Thesis, Royal Holloway, University of London, 1986. http://repository.royalholloway.ac.uk/items/45ee4bfb-9be1-4500-9d03-2b883899c5cb/1/.

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A method has been developed for bromination of aromatic compounds in aqueous solution in an isoperibol calorimeter. The enthalpies of bromination of phenol to 2,4,6-tribromophenol and of aniline, 2-bromo-aniline, 4-bromoaniline and 2,4-dibromoaniline to 2,4,6-tribromo-aniline were measured using this method. These values were used to derive the standard enthalpies of formation of 2,4,6-tribromophenol, 2-bromoaniline, 4-bromoaniline, 2,4-dibromoaniline and 2,4,6-tribromo-aniline. The enthalpies of combustion of 2,4,6-tribromophenol and 2,4,6-tribromoaniline were measured using a rotating-bomb c
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Soper, Jake D. "Reactions at nitrogenous ligands on oxidizing group 8 metal centers /." Thesis, Connect to this title online; UW restricted, 2003. http://hdl.handle.net/1773/8589.

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Olalekan, Temitope Elizabeth. "Synthesis, characterisation and biological activity of 2-(methylthiomethyl)anilines, 2-(methylthio)anilines, their Schiff-base derivatives and metal(II) (Co, Ni, Cu) complexes." Thesis, Rhodes University, 2013. http://hdl.handle.net/10962/d1020868.

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A series of 31 sulfur-nitrogen donor ligands and 64 metal(II) complexes have been investigated. The thiomethylated aniline ligands 2–(methylthiomethyl)aniline 2MT and 2–(methylthio)aniline 2MA were synthesized with their substituted derivatives (-Me, -MeO, -Cl, -Br, -NO2) to serve as chelating agents. These ligands behave as bidentate ligands with SN donor group with Co(II), Ni(II) and Cu(II). The Co(II) and Ni(II) complexes have the ML2Cl2 molecular formula while the Cu(II) complexes formed with MLCl2 stoichiometry where L is the bidentate ligand. The ligands and their metal(II) complexes hav
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Desai, Salil Dileep Kirsch Lee E. "Ortho substitution effects on the acidic and alkaline hydrolyses of formanilides." [Iowa City, Iowa] : University of Iowa, 2009. http://ir.uiowa.edu/etd/353.

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Books on the topic "Anilincs"

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Rappoport, Zvi, ed. The Chemistry of Anilines. John Wiley & Sons, Ltd, 2007. http://dx.doi.org/10.1002/9780470871737.

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Zvi, Rappoport, ed. The chemistry of anilines. Wiley, 2007.

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Canada, Canada Environment Canada, and Canada Health Canada, eds. Aniline. Environment Canada, 1994.

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I, Boeckhout C., Netherlands. Directoraat-Generaal van de Arbeid., and TAUW Infra Consult bv, eds. Werkterreinanalyse van aniline. Directoraat-Generaal van de Arbeid van het Ministerie van Sociale Zaken en Werkgelegenheid, 1991.

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Zok, Sabine. Metabolismus substituierter Aniline beim Zebrabärbling. [s.n.], 1991.

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Great Britain. Health and Safety Executive., ed. Aniline: Risk assessment document EH72/8. HSE Books, 1997.

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United States. Agency for Toxic Substances and Disease Registry. and Research Triangle Institute, eds. Toxicological profile for methylenedianiline. U.S. Dept. of Health and Human Services, Public Health Service, Agency for Toxic Substances and Disease Registry, 1998.

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Syracuse Research Corporation. Center for Chemical Hazard Assessment. Monograph on human exposure to chemicals in the workplace : aniline: Final report. National Cancer Institute, Division of Cancer Etiology, 1985.

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Parzer, Sebastian. Friedrich Engelhorn: BASF-Gründer - Unternehmer - Investor (1865-1902). Wernersche Verlagsgesellschaft, 2014.

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National Institute for Occupational Safety and Health, ed. Morton International Chemical Company, Patterson [i.e. Paterson], New Jersey. U.S. Dept. of Health and Human Services, Public Health Service, Centers for Disease Control and Prevention, National Institute for Occupational Safety and Health, 1994.

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Book chapters on the topic "Anilincs"

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Gooch, Jan W. "Anilides." In Encyclopedic Dictionary of Polymers. Springer New York, 2011. http://dx.doi.org/10.1007/978-1-4419-6247-8_643.

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Lide, David R. "Aniline." In Handbook of Organic Solvents. CRC Press, 2024. http://dx.doi.org/10.1201/9781003575191-18.

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Gooch, Jan W. "Aniline." In Encyclopedic Dictionary of Polymers. Springer New York, 2011. http://dx.doi.org/10.1007/978-1-4419-6247-8_644.

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Patnaik, Pradyot. "Aniline." In Handbook of Environmental Analysis. CRC Press, 2017. http://dx.doi.org/10.1201/9781315151946-69.

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Gooch, Jan W. "Aniline Dye." In Encyclopedic Dictionary of Polymers. Springer New York, 2011. http://dx.doi.org/10.1007/978-1-4419-6247-8_646.

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Gooch, Jan W. "Aniline Ink." In Encyclopedic Dictionary of Polymers. Springer New York, 2011. http://dx.doi.org/10.1007/978-1-4419-6247-8_649.

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Gooch, Jan W. "Aniline Number." In Encyclopedic Dictionary of Polymers. Springer New York, 2011. http://dx.doi.org/10.1007/978-1-4419-6247-8_650.

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Gooch, Jan W. "Aniline Pigments." In Encyclopedic Dictionary of Polymers. Springer New York, 2011. http://dx.doi.org/10.1007/978-1-4419-6247-8_651.

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Gooch, Jan W. "Aniline Point." In Encyclopedic Dictionary of Polymers. Springer New York, 2011. http://dx.doi.org/10.1007/978-1-4419-6247-8_652.

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Gooch, Jan W. "Aniline Printing." In Encyclopedic Dictionary of Polymers. Springer New York, 2011. http://dx.doi.org/10.1007/978-1-4419-6247-8_653.

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Conference papers on the topic "Anilincs"

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Haskaj, Adelina, Musaj Pacarizi, Sonja Lepitkova, Berat Sinan, Bahri Sinani, and Elida Dreshaj. "THE POTENTIAL COMPLEXING IMPACT OF SOME ORGANIC COMPOUNDS AMINE AND CARBOXYL GROUPS ON TRANSITION METALS." In 24th SGEM International Multidisciplinary Scientific GeoConference 24. STEF92 Technology, 2024. https://doi.org/10.5593/sgem2024/4.1/s18.42.

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Environmental water chemistry is substantially aided by modern electrochemical research. Sensitive voltammetric techniques are much more useful for metal species in natural waters, where complexation with organic molecules predominates. Many environmental electrochemists are still interested in determining the stability constants of metal ion complexes with various ionic species found in natural waterways. The aim of this work is to investigate the possible influence of complexation of amine and carboxyl groups of some organic molecules (with EDTA, NTA and aniline, using differential pulse pol
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Sterczewski, Lukasz A., Jakub Mnich, and Jaroslaw Sotor. "Multi-Octave THz Generation and Detection at MHz Repetition Rates using the Organic Nonlinear Crystal PNPA." In CLEO: Science and Innovations. Optica Publishing Group, 2024. http://dx.doi.org/10.1364/cleo_si.2024.sm2p.5.

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Generation and detection of broadband THz radiation using the PNPA ((E)-4-((4-nitrobenzylidene)amino)-N-phenyl-aniline) crystal at MHz repetition rates is demonstrated. Compatibility with nanojoule pump pulses at telecommunication wavelengths makes this medium attractive for compact THz spectrometers.
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Jauhari, Smita, and Bhupendra Mistry. "“Study of the Inhibitive Effect of Novel Quinoline Schiff Base on Corrosion of Mild Steel in HCl Solution”." In CORROSION 2013. NACE International, 2013. https://doi.org/10.5006/c2013-02326.

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Abstract Schiff base 4-Chloro-N-[(2-chloroquinolin-3-yl)methylene]aniline was synthesized, and its inhibitive effect for mild steel in 1M HCl solution was investigated by weight loss measurement and electrochemical tests.From the weight loss measurements and electrochemical tests, it was observed that the inhibition efficiency increases with the increase in the Schiff base concentration and reaches a maximum at the optimum concentration. This is further confirmed by the decrease in corrosion rate. It is found that the system follows Langmuir adsorption isotherm.
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Jauhari, Smita, and Bhupendra Mistry. "Study of the Inhibitive Effect of Novel Schiff Base on Corrosion of HCL on Mild Steel." In CORROSION 2012. NACE International, 2012. https://doi.org/10.5006/c2012-01478.

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Abstract Schiff base (E)-3-chloro-N-((2-chloroquinolin-3-yl)methylene)aniline (CQA) was synthesized, and its inhibitive effect for mild steel in 1M HCl solution was investigated by weight loss measurement and electrochemical tests. From the weight loss measurements and electrochemical tests, it was observed that the inhibition efficiency increases with the increase in the Schiff base concentration and reaches a maximum at the optimum concentration. This is further confirmed by the decrease in corrosion rate. It is found that the system follows Langmuir adsorption isotherm.
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Omotosho, Olugbenga Adeshola, Joshua Olusegun Okeniyi, and Abimbola Patricia Idowu Popoola. "Corrosion Inhibition of Stainless Steel in 0.5 M HCl by C6H5NH2." In CORROSION 2018. NACE International, 2018. https://doi.org/10.5006/c2018-10807.

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Abstract In this study, different concentrations of C6H5NH2 (Aniline) were employed for investigating its corrosion inhibition of stainless steel in 0.5 M HCl. Corrosion rate measurements at 28°C, 45°C and 60°C were obtained from a linear sweep voltametry instrument and analyzed for inhibition efficiency and apparent activation energy in the presence and absence of C6H5NH2. Results showed that C6H5NH2 generally exhibited excellent inhibition effects on stainless steel corrosion at the higher temperatures, i.e. the 45°C and 60°C, at which the self-protectiveness of the stainless steel metal app
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Li, Jie, Boya Zhang, Xuanjie Zhang, Yixuan Li, Xiao Yuan, and Xingwen Li. "Effect of Large Linking Groups on the Electrical and Thermal Properties of Aniline Cured Epoxy Resins." In 2024 3rd International Conference on Power Systems and Electrical Technology (PSET). IEEE, 2024. https://doi.org/10.1109/pset62496.2024.10808806.

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Kon, Yoshihiro. "Selective monoallylation of anilines to form fine chemicals using allyl alcohol derived from glycerol." In 2022 AOCS Annual Meeting & Expo. American Oil Chemists' Society (AOCS), 2022. http://dx.doi.org/10.21748/mjrr3569.

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Glycerol is an important starting material for the production of value-added chemicals such as electronic materials and pharmaceuticals. We herein present a selective allylation reaction using allyl alcohol which is given from glycerol. First, we show the rhenium catalyzed high-yielding synthesis of allyl alcohol from glycerol through deoxydehydration reaction. Next, the selective N-allyl aniline synthesis from allyl alcohol with aniline is performed. The well-dispersed tungsten oxide supported on zirconium oxide can catalyze the reaction to produce the corresponding mono-allyl compound over
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Pattanayak, Soumya Sundar, Tushar Bachhar, and Swagatadeb Sahoo. "Dielectric Relaxation Phenomena of Aniline and Substituted Anilines with Acetonitrile Under 9.36 GHz Electric Field." In 2018 3rd International Conference for Convergence in Technology (I2CT). IEEE, 2018. http://dx.doi.org/10.1109/i2ct.2018.8529794.

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Yan, Shuxin, and Lee H. Spangler. "Nitrogen inversion mode in substituted anilines." In OSA Annual Meeting. Optica Publishing Group, 1992. http://dx.doi.org/10.1364/oam.1992.tul9.

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Antonac, Irena, Pavle Trošelj, Davor Margetić, Zoran Glasovac, and Mirjana Eckert-Maksić. "Microwave assisted carboxymethylation of anilines and phenols." In The 10th International Electronic Conference on Synthetic Organic Chemistry. MDPI, 2006. http://dx.doi.org/10.3390/ecsoc-10-01439.

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Reports on the topic "Anilincs"

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Feng, J., W. Zhang, A. G. MacDiarmid, and A. J. Epstein. Synthesis and Characterization of Oligomeric Anilines. Defense Technical Information Center, 1997. http://dx.doi.org/10.21236/ada330138.

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Zhou, H. C., and R. S. Duran. The Effect of Surface Pressure on Langmuir-Blodgett Polymerization of 2- Pentadecyl Aniline. Defense Technical Information Center, 1992. http://dx.doi.org/10.21236/ada250993.

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Bernstein, E. R., M. F. Hineman, S. K. Kim, and D. F. Kelley. Vibrational Dynamics of Aniline (N2)1 Clusters in Their First Excited Singlet State. Defense Technical Information Center, 1992. http://dx.doi.org/10.21236/ada245812.

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Huang, S. X., J. L. Gland, and D. A. Fischer. Aniline hydrogenolysis on the Pt(111) single crystal surface: Mechanisms for C-N bond activation. Office of Scientific and Technical Information (OSTI), 1993. http://dx.doi.org/10.2172/10117539.

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Essington, M. E., J. M. Bowen, R. A. Wills, and B. K. Hart. Adsorption of aniline and toluidines on montmorillonite: Implications for the disposal of shale oil production wastes. Office of Scientific and Technical Information (OSTI), 1992. http://dx.doi.org/10.2172/6745527.

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Essington, M. E., J. M. Bowen, R. A. Wills, and B. K. Hart. Adsorption of aniline and toluidines on montmorillonite: Implications for the disposal of shale oil production wastes. Office of Scientific and Technical Information (OSTI), 1992. http://dx.doi.org/10.2172/10133217.

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Ruangpornvisuti, Vithaya. Basicity investigation and structure optimization of polyaza-Calixarenes and stabilities of their complexes with metal cations. Chulalongkorn University, 2000. https://doi.org/10.58837/chula.res.2000.26.

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Abstract:
The structure of 25, 26, 27, 28-tetra(2-ethoxyaniline)calix[4]arene of cone (cL) and partial cone (pcL) conformations were optimized by PM3 of quantum chemical method. It has been found that cL structure is more stable than pcL conformation. The stabilization energies of protonation on four aniline-nitrogen atoms of both conformations of the ligand at 6-31G energy level, were obtained. The protonations process on the cL and pcL being 7 and 24 possible pathways, respectively, were evaluated. The basicity constants of partial cone conformation of 25, 26, 27, 28-tetra(2- ethoxyaniline)calix[4]are
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NIOSH skin notation (SK) profile: aniline [CAS No. 62-53-3]. U.S. Department of Health and Human Services, Public Health Service, Centers for Disease Control and Prevention, National Institute for Occupational Safety and Health, 2015. http://dx.doi.org/10.26616/nioshpub2015192.

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Request for assistance in preventing bladder cancer from exposure to o-toluidine and aniline. U.S. Department of Health and Human Services, Public Health Service, Centers for Disease Control, National Institute for Occupational Safety and Health, 1990. http://dx.doi.org/10.26616/nioshpub90116.

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