Relevant bibliographies by topics / Reaction of aniline

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

Academic literature on the topic 'Reaction of aniline'

Author: Grafiati
Published: 5 June 2025
Last updated: 1 August 2025

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Journal articles on the topic "Reaction of aniline"

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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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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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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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Heichert, Christoph, and Horst Hartmann. "On the Formation of Mauvein: Mechanistic Considerations and Preparative Results." Zeitschrift für Naturforschung B 64, no. 6 (2009): 747–55. http://dx.doi.org/10.1515/znb-2009-0622.

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The reaction of aniline (AH2) with an oxidizing agent in acidic solution gives rise to the formation of a mixture of products containing, besides a variety of oligoanilines named as Aniline Black or Polyaniline, Mauvein as a deeply purple phenazine derivative. Although this Mauvein synthesis was developed by W.H. Perkin more than 150 years ago and has opened the era of industrial dyestuff chemistry, the detailed mechanism of this reaction has remained rather unclear until today. The elucidation of the mechanism of the Mauvein formation as an oxidative coupling process of AH2 is hindered by the
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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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Asheri, Osman, Sayyed Mostafa Habibi-Khorassani, and Mehdi Shahraki. "A Study on the Kinetics and Mechanism of the One-Pot Formation of 3,4,5-Substituted Furan-2(5H)-Ones in the Presence of Lactic Acid: Effect of Different Substituents." Progress in Reaction Kinetics and Mechanism 43, no. 3-4 (2018): 286–99. http://dx.doi.org/10.3184/146867818x15319903829218.

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The kinetics of the reaction between para-substituted anilines and dimethyl acetylenedicarboxylate (DMAD) with derivatives of benzaldehyde for the one-pot formation of 3,4,5-substituted furan-2(5 H)-ones in the presence of lactic acid as a catalyst have been studied spectrophotometrically at different temperatures. A mechanism involving four steps was proposed for the reactions, all of which followed second-order kinetics. The partial orders with respect to substituted aniline and DMAD were one and one and the reactions revealed zero-order kinetics for benzaldehyde and its derivatives. Changin
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Huang, Jun, Linyong Li, Haoguo Chen, Tiebo Xiao, Yuwei He, and Lei Zhou. "Silver-catalyzed geminal aminofluorination of diazoketones with anilines and N-fluorobenzenesulphonimide." Organic Chemistry Frontiers 4, no. 4 (2017): 529–33. http://dx.doi.org/10.1039/c6qo00813e.

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A silver-catalyzed three-component reaction of diazoketones, anilines and NFSI is developed. The reaction provides a new method for gem-aminofluorination of acceptor diazo compounds with aniline as the nitrogen source and NFSI as the fluorine source.
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Al-Howsaway, Hamida O. M., Magda F. Fathalla, Ali A. El-Bardan, and Ezzat A. Hamed. "Reaction of 4-Chloro-3,5-Dinitrobenzotrifluoride with Aniline Derivatives. Substituent Effects." Journal of Chemical Research 2007, no. 9 (2007): 509–12. http://dx.doi.org/10.3184/030823407x240926.

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N-(2,6-Dinitro-4-trifluoromethylphenyl)aniline derivatives were prepared by anilino-dechlorination of 4-chloro-3, 5-dinitrobenzotrifluoride. IR, UV and 1H NMR studies suggested an intramolecular hydrogen bond between the amino hydrogen and one o-nitro group. An addition-elimination mechanism was suggested based on the second-order kinetics and the dependence of rates on the nature and the position of the substituent in the aniline ring, as well as the high negative values of ρ(-3.14, −3.16, −3.01). Such values indicate a positive charge on the aniline nitrogen in the transition state and that
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Qin, Ling, G. N. R. Tripathi, and Robert H. Schüler. "Radiation Chemical Studies of the Oxidation of Aniline in Aqueous Solution." Zeitschrift für Naturforschung A 40, no. 10 (1985): 1026–39. http://dx.doi.org/10.1515/zna-1985-1009.

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Oxidation of aniline in aqueous solution by ·OH radicals proceeds predominantly via addition to the ring followed by elimination of OH- on the microsecond time scale to form the aniline radical cation. Direct oxidation by electron transfer accounts for less than 4% of the ·OH reactions. The different hydroxycyclohexadienyl isomers produced by ·OH addition decay at different rates with this decay catalyzed both by protons and phosphate. In basic solution the resultant radical cation deprotonates to form the anilino radical. The p Ka for the equilibrium between the acidic and basic forms of this
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Holze, Rudolf. "Radical Intermediates in Electrochemical Polymer-Forming Reactions." Collection of Czechoslovak Chemical Communications 65, no. 6 (2000): 899–923. http://dx.doi.org/10.1135/cccc20000899.

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The role of organic radicals in the formation of functional polymers, in particular intrinsically conducting polymers, is reviewed. New results recently obtained with in situ spectroscopic methods illustrating the influence of the molecular structure of monomers (aniline and substituted anilines) in the behaviour of radical intermediates are presented. The stabilising influence of substituents at various positions of the aniline molecule is evaluated and compared based on conceivable structures of reaction intermediates.
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Dissertations / Theses on the topic "Reaction of aniline"

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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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Rannou, Patrice. "Poly(aniline) : synthèse, mise en oeuvre et vieillissement." Université Joseph Fourier (Grenoble ; 1971-2015), 1998. http://www.theses.fr/1998GRE10080.

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Ce travail est consacré à la synthèse, la mise en œuvre et le vieillissement d'un polymère conducteur (pc) : la polyaniline (pani). Deux morphologies ont été étudiées : des poudres divisées de pani dopee par l'acide chlorhydrique (pani-hci) et des films de pani dopee par l'acide camphre sulfonique (csa) obtenus par l'évaporation de solutions dans le m-cresol. Dans une première partie, nous présentons la synthèse chimique basse température par voie oxydante de la pani. Le contrôle des paramètres de synthèse a permis de préciser le mécanisme de polymérisation et d'obtenir des polymères de masse
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Doridot, Gabriel. "Etude de la transformation d'aminocyclopropanes élaborés dans le cadre d'une stratégie de synthèse de 14-azastéroïdes." Phd thesis, Université Paris Sud - Paris XI, 2011. http://tel.archives-ouvertes.fr/tel-00937934.

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Au cours de ces travaux de thèse, une voie de synthèse de différentes cyclopropylamines a été développée. Leur fonctionnalisation a ensuite été mise en œuvre à l'aide de réactions de métallation ou de couplages croisés catalysés au palladium. Les cyclopropylamines ainsi fonctionnalisées furent alors soumises à des conditions de cyclisation dans le but d'obtenir tout ou partie d'une structure 14-azastéroïde. Si notre modèle, dont la synthèse s'est construite autour d'une aniline, nous a permis d'obtenir la structure des cycles B, C et D d'un 14-azastéroïde, nous n'avons pas été en mesure d'obte
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Rabbitt, Lynsey C. "Some kinetic and equilibrium studies of the reactions of nitrobenzofurazan derivatives with nucleophiles." Thesis, Durham University, 2000. http://etheses.dur.ac.uk/4623/.

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The reactions of 4,6-dinitrobenzofuroxan, (DNBF) with aniline and six of its N- and ring- substituted derivatives have been studied. It is known that aniline usually reacts as a nitrogen nucleophile, forming nitrogen-bonded σ-adducts with trinitrobenzene, (TNB) in the presence of a strong base. However, in acidic solutions, a-adducts are formed with bonding between a ring carbon atom of the anilines and the 7-position of DNBF. A value of 2.0 for k(_H)/k(_D), the kinetic isotope effect, indicates that bond formation is largely rate determining in the substitution pathway. Estimates were made fo
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RAMADAN, DOAA REDA MOHAMED. "PALLADIUM CATALYZED REACTIONS: REDUCTIVE CYCLIZATION OF NITROARENES, AND OXIDATIVE CARBONYLATION OF ANILINE." Doctoral thesis, Università degli Studi di Milano, 2021. http://hdl.handle.net/2434/819652.

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Palladium Catalyzed Reactions: Reductive Cyclization of Nitroarenes, and Oxidative Carbonylation of Aniline Abstract: The thesis is divided into two main chapters: reductive cyclization of nitroarenes, and oxidative carbonylation of aniline. The first chapter involves developing a catalytic system for carbazoles synthesis through reductive cyclization of 2-nitrobiphenyls employing phenyl formate as an in-situ source of CO. Thus, the synthetic chemist can avoid handling pressurized CO lines and perform the reaction in a pressure tube, a cheap and readily available tool for any laborat
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Radianingtyas, Helia. "Development of a biofilm reactor process for the treatment of 4-chloroaniline." Thesis, University of Kent, 2000. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.314266.

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Mendiratta, Arjun. "Reductive coupling and related reactions with Mo and Ti tris- anilides." Thesis, Massachusetts Institute of Technology, 2005. http://hdl.handle.net/1721.1/32483.

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Thesis (Ph. D.)--Massachusetts Institute of Technology, Dept. of Chemistry, 2005.<br>Vita.<br>Includes bibliographical references.<br>Chapter 1: The capability of Mo(N[t-BulAr)₃ to act as a powerful one, two, and three electron reductant have been previously demonstrated. In this work, we show that Mo(NIt-BulAr)₃ forms a metastable adduct with the moderate [pi] acid PhCN; coordination of PhCN activates the nitrile carbon towards reaction with a variety of one-electron reagents such as dichalcogenides, nitric oxide, hydrogen atom donors, cobaltocene, and elemental phosphorus. Evidence is presen
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ELKACEMI, KACEM. "Etude electrochimique de divers conducteurs organiques." Paris 6, 1986. http://www.theses.fr/1986PA066399.

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Etude electrochimique des sels de radicaux ioniques organiques, des complexes par transfert de charge et des radicaux ioniques. Donnees sur les composes conducteurs, formes par oxydation du tetrathiofulvalene (ttf) en presence de differents anions (scn**(-), no::(3)**(-) et mncl::(3)**(-)), par oxydation de tmttf dans l'acetonitrile en presence de scn**(-) et par reduction de tcnq en presence de differents cations. Donnees, aussi, sur les proprietes optiques et electrochimiques des films conducteurs de polyaniline
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HADDAD-FAHED, OMAIMA. "Catalyse micellaire de reactions de substitution nucleophile aromatique comportant des reactifs electriquement charges." Paris 6, 1987. http://www.theses.fr/1987PA066419.

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Liu, Kun. "Catalytic Asymmetric Synthesis of Chiral Cyclic Amines and Axially Chiral Anilides by Phase-Transfer Catalyzed Reactions." 京都大学 (Kyoto University), 2012. http://hdl.handle.net/2433/158098.

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Books on the topic "Reaction of aniline"

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Simard, Robert D. An EPR study of the intermediates formed in the reaction between aluminium atoms and aniline. Laurentian University, 2005.

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Wroby, Norman William. Reaction Between Dimethyl Aniline and Benzene Sulfonyl Chloride. Creative Media Partners, LLC, 2021.

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Aniline: Structural/Physical Properties, Reactions and Environmental Effects. Nova Science Pub Inc, 2013.

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Book chapters on the topic "Reaction of aniline"

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Sharma, Virender K., Zoltan Homonnay, Karolina Siskova, Libor Machala, and Radek Zboril. "Mössbauer investigation of the reaction of ferrate(VI) with sulfamethoxazole and aniline in alkaline medium." In LACAME 2012. Springer Netherlands, 2013. http://dx.doi.org/10.1007/978-94-007-6482-8_1.

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Itakura, Ryuji, Jun Watanabe, Taiki Asano, and Kaoru Yamanouchi. "Reaction dynamics of hydrogen bonded aniline-ammonia clusters in intense laser fields by tandem mass spectroscopy." In Ultrafast Phenomena XIII. Springer Berlin Heidelberg, 2003. http://dx.doi.org/10.1007/978-3-642-59319-2_33.

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Gallego, Mar Gómez, and Miguel A. Sierra. "Level 3 - Case 39 Periodinane-Mediated Cyclization of Anilides." In Organic Reaction Mechanisms. Springer Berlin Heidelberg, 2004. http://dx.doi.org/10.1007/978-3-642-18788-9_39.

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Doraiswamy, L. K. "Reactor Design for Complex Reactions." In Organic Synthesis Engineering. Oxford University Press, 2001. http://dx.doi.org/10.1093/oso/9780195096897.003.0018.

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Procedures were formulated in Chapter 5 for treating complex reactions. We now turn to the design of reactors for such reactions. Continuing with the ethylation reaction, we consider the following reactor types for which design procedures were formulated earlier in Chapter 4 for simple reactions: batch reactors, continuous stirred reactors (or mixed-flow reactors), and plug-flow reactors. However, we use the following less formal nomenclature: A = aniline, B = ethanol, C = monoethyaniline, D = water, E = diethylaniline, F = diethyl ether, and G = ethylene. The four independent reactions then b
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Aitken, R. A. "Reaction of a Hindered Aniline with Selenium Oxychloride." In Five-Membered Hetarenes with Three or More Heteroatoms. Georg Thieme Verlag KG, 2004. http://dx.doi.org/10.1055/sos-sd-013-01224.

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Yamazaki, S., and K. Yamamoto. "Condensation Reaction of the Carboxy Group with Aniline Derivatives." In Six-Membered Hetarenes with Two Unlike or More than Two Heteroatoms and Fully Unsaturated Larger-Ring Heterocycles. Georg Thieme Verlag KG, 2004. http://dx.doi.org/10.1055/sos-sd-017-00016.

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B, Suresh, and Dr G. Vanmathi. "CATALYTIC ACTIVITY OF ELECTRON BEAM IRRADIATED Pd/C ON 2-METHYL NITRO BENZENE." In Futuristic Trends in Chemical Material Sciences & Nano Technology Volume 3 Book 15. Iterative International Publishers, Selfypage Developers Pvt Ltd, 2024. http://dx.doi.org/10.58532/v3becs15p8ch2.

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In this study nitro compounds viz., 2 – methyl nitro benzene was reduced by 10% Pd/C (50% wet) to 2 – methyl aniline and it is confirmed from MASS and NMR studies. The product yield was 70%. The hydrogenation was complete in 9.30 h. The catalysts were then irradiated by electron beam to various dosages from 0 kGy, 150 kGy, 200 kGy and 250 kGy using Microtron &amp; RF Linac. The reduction reactions were conducted under similar conditions using irradiated 10% Pd/C samples. Now the product yield was 93%. The hydrogenation was fast and completed within 2 h 30 min. With the electron beam irradiated
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Taber, Douglass F. "Substituted Benzenes: The Alvarez- Manzaneda Synthesis of (–)-Akaol A." In Organic Synthesis. Oxford University Press, 2015. http://dx.doi.org/10.1093/oso/9780190200794.003.0063.

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Ramin Ghorbani-Vaghei of Bu-Ali Sina University devised (Tetrahedron Lett. 2012, 53, 2325) conditions for the bromination of an electron-deficient arene such as 1. Yonghong Gu of the University of Science and Technology of China found (Tetrahedron Lett. 2011, 52, 4324) that an electron-rich anilide 3 could be oxidized to 4. Sukbok Chang of KAIST (J. Am. Chem. Soc. 2012, 134, 2528) and Kouichi Ohe of Kyoto University (Chem. Commun. 2012, 48, 3127) devised protocols for the oxidative cyanation of 5 to 6. Phenylazocarboxylates and triazenes are stable, but have the reaction chemistry of diazonium
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Doraiswamy, L. K. "Catalysis by Solids, 2 : The Catalyst and Its Microenvironment." In Organic Synthesis Engineering. Oxford University Press, 2001. http://dx.doi.org/10.1093/oso/9780195096897.003.0013.

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Solid catalysts by their very nature involve diffusion of reactant fluids within their matrix. These fluids react even as they diffuse. Thus the problem of internal diffusion accompanied by reaction becomes important. Another problem of equal importance is the transport of the reactant from the fluid bulk to the catalyst surface—often referred to as external diffusion. Together these constitute the microenvironment of the catalyst pellet and form the subject matter of this chapter. Consider the reaction between aniline and methanol on pellets of alumina to give dimethylaniline: Let the pellets
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Patel, Ashok Raj, Geetika Patel, Arti Srivastava, Bhaskar Sharma, Goutam Kumar Patra, and Subhash Banerjee. "Nano-Catalysis in the Selective Oxidation of Alcohols and Anilines." In Diverse Strategies for Catalytic Reactions. BENTHAM SCIENCE PUBLISHERS, 2023. http://dx.doi.org/10.2174/9789815079036123020004.

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Recently, the development of eco-friendly and sustainable organic redox reactions has attracted considerable attention. In the classification of catalysis, the two categories, homogeneous and heterogeneous catalysis, have their own advantages and limitations. Thus, we need catalytic species that show properties like homogeneous and heterogeneous catalysts. Nano-catalysts fulfill the above requirements as it works as a “linker” between the homogeneous and heterogeneous catalysts. In past years, various heterogeneous nanomaterials have been used in different organic transformations as green cata
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Conference papers on the topic "Reaction of aniline"

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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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Quattrociocchi, Daniel Garcez Santos, Antonio Rafael de Oliveira, Douglas da Motta Pio, and Vinicius Rangel Campos. "Estudo teórico da formação da isatina e de seus derivados dimetoxilados pelo método Sandmeyer." In VIII Simpósio de Estrutura Eletrônica e Dinâmica Molecular. Universidade de Brasília, 2020. http://dx.doi.org/10.21826/viiiseedmol2020109.

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Isatin has been attracted the researchers attention due the structural versatility and can be used to synthesized other molecules with pharmacological activities. The Sandmeyer method is one of the most common methods for the synthesis of this molecule. Where the reaction with from aniline with chloral hydrate and hydroxyl amine occurs with good yield. When the same reaction is performed with dimethoxylated aniline show low yield or is not observed experimentally. These observations motivate this work and the justification for these facts are given in terms of thermodynamic parameters and by t
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Itakura, Ryuji. "Reaction dynamics of aniline-ammonia cluster ions in intense laser fields by tandem mass spectroscopy." In SCIENCE OF SUPERSTRONG FIELD INTERACTIONS: Seventh International Symposium of the Graduate University for Advanced Studies on Science of Superstrong Field Interactions. AIP, 2002. http://dx.doi.org/10.1063/1.1514287.

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Itakura, Ryuji, Jun Watanabe, Taiki Asano, and Kaoru Yamanouchi. "Reaction dynamics of hydrogen bonded aniline-ammonia clusters in intense laser fields by tandem mass spectroscopy." In International Conference on Ultrafast Phenomena. OSA, 2002. http://dx.doi.org/10.1364/up.2002.me13.

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de Lange, M. C. C., D. Thorn Leeson, A. H. Huizer, and C. A. G. O. Varma. "Features of the Dual Fluorescence of 4-N,N-dialkylaminoalkylbenzoates in Alkanes." In International Conference on Ultrafast Phenomena. Optica Publishing Group, 1992. http://dx.doi.org/10.1364/up.1992.mc34.

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The appearance of a normal band FN and an anomalous band Fx, to the red of the former, in the fluorescence spectrum of solutions of 4-N,N-diethylaminoethylbenzoate in alkanes has been considered as evidence for the existence of a low energy twisted intramolecular charge transfer (TICT) excited state in electron acceptor substituted aniline derivatives [1]. Objections have been raised against this interpretation of the dual fluorescence [2]. Nevertheless, the TICT state seems to be widely accepted as a reasonable explanation of the phenomenon. Here we will present evidence that the long wavelen
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Chen, Dr Bin. "Green Hydrogen Production From Pig Manure Gasification in Supercritical Water." In 8th World Conference on Chemistry and Chemical Engineering and 8th World Conference on Advanced Materials, Nanoscience and Nanotechnology. Eurasia Conferences, 2025. https://doi.org/10.62422/978-81-981865-7-7-016.

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The world can produce 7.27×109 Kg of pig manure in only one year. Between 2018 and 2020, China's major livestock produced 1.27×1010 Kg of manure annually, of which pig manure accounted for one-eighth. Pig manure is overflowing with HMs, Escherichia coli, nitrogen, phosphorus, and carbon, contributing to global climate change and environmental pollution through nitrous oxide, ammonia, and bioaccumulation. Supercritical water gasification (SCWG) technology can convert pig manure into green hydrogen or hydrogen-rich gas, which has immense potential in waste-to-wealth conversion while controlling
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Feng, Hao, Xun Zhu, Rong Chen, and Qiang Liao. "Visualization Study on Two-Phase Flow Behaviors in the Gas-Liquid-Solid Microreactor for Hydrogenation of Nitrobenzene." In ASME 2016 Fluids Engineering Division Summer Meeting collocated with the ASME 2016 Heat Transfer Summer Conference and the ASME 2016 14th International Conference on Nanochannels, Microchannels, and Minichannels. American Society of Mechanical Engineers, 2016. http://dx.doi.org/10.1115/fedsm2016-1011.

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In this study, visualization study on the gas-liquid two phase flow characteristics in a gas-liquid-solid microchannel reactor was carried out. Palladium nanocatalyst was coated onto the polydopamine functionalized surface of the microchannel through eletroless deposition. The materials characterization results indicated that palladium nanocatalyst were well dispersed on the modified surface. The effects of both the gas and liquid flow rates as well as inlet nitrobenzene concentration on the two-phase flow characteristics were studied. The experimental results revealed that owing to the chemic
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Kinaci, Emre, Giuseppe Palmese, Joseph Stanzione, and Sarah Salazar. "Evaluation of hybridized bio-based building blocks as coating materials." In 2022 AOCS Annual Meeting & Expo. American Oil Chemists' Society (AOCS), 2022. http://dx.doi.org/10.21748/oyjf3899.

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Commercial epoxy resins are often the oligomeric reaction products of bisphenol A (BPA) with epichlorohydrin. BPA is a toxic petrochemical and a well-known endocrine disruptor which can mimic the body’s own hormones and may lead to several negative health effects. The most common curing agents are also the derivatives of toxic amines such as aniline, ethylene di-amine, and ammonia etc. which are under strict regulations and restrictions by TSCA and (REACH) agencies. Therefore; there is a growing demand to develop epoxy and amine systems from non- or less- toxic and annually renewable precurs
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9

Stadlbauer, Wolfgang, and Naresh Badgujar. "Reactions of Acetoacetates With Electron-deficient Anilines." In The 11th International Electronic Conference on Synthetic Organic Chemistry. MDPI, 2007. http://dx.doi.org/10.3390/ecsoc-11-01330.

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10

Aribowo, Slamet, Mas Ayu Elita Hafizah, Azwar Manaf, and Andreas. "Study of aniline polymerization reactions through the particle size formation in acidic and neutral medium." In PROCEEDINGS OF THE 3RD INTERNATIONAL CONFERENCE ON MATERIALS AND METALLURGICAL ENGINEERING AND TECHNOLOGY (ICOMMET 2017) : Advancing Innovation in Materials Science, Technology and Applications for Sustainable Future. Author(s), 2018. http://dx.doi.org/10.1063/1.5030278.

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