2019
DOI: 10.1016/j.molstruc.2019.06.070
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Performance and computational studies of two soluble pyran derivatives as corrosion inhibitors for mild steel in HCl

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Cited by 92 publications
(26 citation statements)
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“…Figure 2 represents the inhibition efficiency and the corrosion rate of the studied inhibitor KYNA. This inference establish the prosperous inhibitory action for the KYNA is obtained which should be attributed to the formation of a protective film at the metal/solution interface [13] Electrochemical experiments…”
Section: Weight Loss Studiessupporting
confidence: 56%
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“…Figure 2 represents the inhibition efficiency and the corrosion rate of the studied inhibitor KYNA. This inference establish the prosperous inhibitory action for the KYNA is obtained which should be attributed to the formation of a protective film at the metal/solution interface [13] Electrochemical experiments…”
Section: Weight Loss Studiessupporting
confidence: 56%
“…From Fig. 6, it can be seen that with the addition of KYNA, both the anodic as well as cathodic curves shifted toward lower current density, which indicates that in the presence of KYNA, both the anodic dissolution of iron and the cathodic evaluation of hydrogen gas are inhibited [13]. These experimental results indicate that the addition of KYNA may affect the anodic and the cathodic corrosion reaction.…”
Section: Electrochemical Polarization (Ep) Studiesmentioning
confidence: 81%
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“…Inhibitive ability, which is denoted by η % is remarkably increased with the addition of CI leaf extract. It suggests that there is an adsorption of CI leaf extract molecules and the formation of a protective film on the surface of mild steel [35]. In addition to the results, it is found from the literature that if E corr is greater than ± 85 mV / SCE compared to the blank acid solution, the inhibitor may be classified as a cathodic or anodic type whereas, if the E corr value is less than ± mV / SCE, the inhibitor may be classified as a mixed type [36].…”
Section: Potentiodynamic Polarization Measurementsmentioning
confidence: 99%
“…In contrast, in 4H-pyran, the saturated carbon is in position 4. 4Hpyran was first isolated, prepared and distinguished in 1962 by the pyrolysis of 2acetoxy-3,4-dihydro-2H-pyran [4], and found to be very unstable, particularly in the presence of air, 4H-pyran does not readily match the corresponding dihydropyran and beryllium ion, which readily decomposes in an aqueous medium [5]. Although pyrenes themselves are of little importance in chemistry, many of their derivatives are essential biological molecules [6], such as pyranoflavonoids, and pyranones are also important derivatives, which are natural products, an example of which is coumarin [7].…”
Section: Introductionmentioning
confidence: 99%