2013
DOI: 10.1016/j.corsci.2012.11.031
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Corrosion inhibition of carbon steel using novel N-(2-(2-mercaptoacetoxy)ethyl)-N,N-dimethyl dodecan-1-aminium bromide during acid pickling

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Cited by 254 publications
(87 citation statements)
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“…In each experiment, triplicate samples of the precleaned and weighed MS substrates were freely suspended in different test solutions. The test MS substrates were recovered after 24 of immersion, thoroughly cleaned using the chemical method for cleaning rust products as previously reported [14], and reweighed using a digital analytical balance with a sensitivity of 0.1 mg. The standard deviation values among parallel triplicate experiments were found to be smaller than 5%, indicating good reproducibility.…”
Section: Corrosion Studiesmentioning
confidence: 99%
“…In each experiment, triplicate samples of the precleaned and weighed MS substrates were freely suspended in different test solutions. The test MS substrates were recovered after 24 of immersion, thoroughly cleaned using the chemical method for cleaning rust products as previously reported [14], and reweighed using a digital analytical balance with a sensitivity of 0.1 mg. The standard deviation values among parallel triplicate experiments were found to be smaller than 5%, indicating good reproducibility.…”
Section: Corrosion Studiesmentioning
confidence: 99%
“…Recently, more corrosion publications contained substantial quantum chemical calculations and molecular dynamics simulations [98][99][100]. Such calculations are usually used to explore the relationship between the inhibitor molecular properties and their corrosion inhibition efficiencies.…”
Section: Quantum Chemical Studies and Molecular Modeling Approachesmentioning
confidence: 99%
“…This might be due to the fact that amine groups act as bases in the strong acidic medium. 13 In the case of corrosion rates, since they show the same trend as the I corr values, they are not discussed further here. Figure 2(a) that the I corr values of Tris-C n decrease as the concentration of Tris-C n increases, implying that the retardation of corrosion takes place in this system.…”
Section: Resultsmentioning
confidence: 90%
“…For the synthesis of 2,4,6-tris(n-carboxyalkylamino)-1,3,5-triazine, cyanuric chloride (Aldrich, 99%, St. Louis, MO, USA), glycine (Sigma, ≥99%, St. Louis, MO, USA), β-alanine (Aldrich, 99%), γ-aminobutyric acid (Sigma, ≥99%), 5-aminopentanoic acid (Aldrich, 97%), 6-aminocaproic acid (Sigma, ≥99%) were used. The chemical structures of 2,4,6-tris(n-carboxyalkylamino)-1,3,5-triazine derivatives were characterized by using 300 MHz 1 H NMR and 13 C NMR (Bruker, Cambridge, UK), FTS165 FT-IR (Bio-Rad, Hercules, CA, USA), 1112 Series flash elemental analyzer (EA) (Thermo Finnigan, Pipersville, PA, USA), and JMS-700 and JMS-DX303 mass spectrometer (MS) (Jeol, Tokyo, Japan) instruments. As the NMR solvent, deuterated trifluoroacetic acid (TFA-d 4 ) or dimethyl sulfoxide (DMSO-d 6 ) was used, and tetramethylsilane was used as the internal standard for calibrating the chemical shifts of The 2,4,6-tris(n-carboxyalkylamino)-1,3,5-triazine derivatives were prepared by a nucleophilic aromatic substitution reaction (S N Ar) of a primary amine with cyanuric chloride.…”
Section: Methodsmentioning
confidence: 99%