Significance of Hammett and Taft substituent constants on bonding potential of organic corrosion inhibitors: Tailoring of reactivity and performance
By changing the electron density at donor sites (also called adsorption or coordination sites),
the substituents significantly impact the coordination proficiency of organic inhibitors. The …
the substituents significantly impact the coordination proficiency of organic inhibitors. The …
Substituents effect on corrosion inhibition performance of organic compounds in aggressive ionic solutions: a review
One of the factors that limit the use of synthetic organic compounds as corrosion inhibitors is
the series of trials associated with traditional syntheses that have to be carried out in the …
the series of trials associated with traditional syntheses that have to be carried out in the …
Corrosion inhibition of steel using different families of organic compounds: Past and present progress
Application of organic compounds as corrosion inhibitors, particularly heterocyclic
compounds, is one of the most economical and effective corrosion mitigation methods of …
compounds, is one of the most economical and effective corrosion mitigation methods of …
[PDF][PDF] Evaluation of performance of corrosion inhibitors using adsorption isotherm models: an overview
E Ituen, O Akaranta, A James - Chem. Sci. Int. J, 2017 - researchgate.net
Adsorption isotherm models are an important tool for describing interaction of corrosion
inhibitors with metal surfaces which they are aimed to protect. In this paper, key adsorption …
inhibitors with metal surfaces which they are aimed to protect. In this paper, key adsorption …
Colloidal and interface aqueous chemistry of dyes: Past, present and future scenarios in corrosion mitigation
The most effective corrosion inhibitors are organic compounds, especially heterocyclic ones
with a certain balance of hydrophilicity, hydrophobicity, and conjugation. Most dyes develop …
with a certain balance of hydrophilicity, hydrophobicity, and conjugation. Most dyes develop …
Imidazoles as highly effective heterocyclic corrosion inhibitors for metals and alloys in aqueous electrolytes: A review
Imidazole represents a special class of heterocyclic compounds that possesses several
industrial and biological activities. Imidazole and its derivatives are extensively employed as …
industrial and biological activities. Imidazole and its derivatives are extensively employed as …
A detailed experimental performance of 4-quinolone derivatives as corrosion inhibitors for mild steel in acid media combined with first-principles DFT simulations of …
CM Fernandes, ARP Costa, MC Leite, V Martins… - Journal of Molecular …, 2023 - Elsevier
Abstract Four 4-oxo-1, 4-dihydroquinoline-3-carboxylate derivatives were synthesized
through the Gould-Jacobs method and evaluated as corrosion inhibitors for 1020 mild steel …
through the Gould-Jacobs method and evaluated as corrosion inhibitors for 1020 mild steel …
1-(4-Nitrophenylo-imino)-1-(phenylhydrazono)-propan-2-one as corrosion inhibitor for mild steel in 1 M HCl solution: weight loss, electrochemical, thermodynamic and …
(4-Nitrophenylo-imino)-1-(phenylhydrazono)-propan-2-one (NO 2 AM) was studied as a
corrosion inhibitor for mild steel in 1 M HCl solution by weight loss, polarization …
corrosion inhibitor for mild steel in 1 M HCl solution by weight loss, polarization …
Recent advancements in corrosion inhibitor systems through carbon allotropes: Past, present, and future
Nano‐sized carbon allotropes, particularly graphene (G), graphene oxide (GO), single and
multi‐walled carbon nanotubes (CNTs, SWCNTs, and MWCNTs) and their chemically …
multi‐walled carbon nanotubes (CNTs, SWCNTs, and MWCNTs) and their chemically …
Experimental and theoretical investigation of the inhibitory effect of new pyridazine derivatives for the corrosion of mild steel in 1 M HCl
The effects of four pyridazine derivatives namely, 2-(6-chloropyridazin-3-yl)-2-
phenylacetonitrile (P1), 3-(6-chloro-3-pyridazinyl)-1H-indole (P2), 4-(6-chloropyridazin-3-yl) …
phenylacetonitrile (P1), 3-(6-chloro-3-pyridazinyl)-1H-indole (P2), 4-(6-chloropyridazin-3-yl) …