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The aim of this investigation was to compare the performance of three typical oil field carbon dioxide corrosion inhibitors in controlling preferential weld corrosion (PWC) of X65 pipeline steel in artificial seawater (3.5 weight per cent) saturated with carbon dioxide at one bar pressure.

A novel rotating cylinder electrode (RCE) apparatus was used to evaluate the effect of flow on the inhibition for the weld metal (WM), heat-affected zone (HAZ) and parent material. To fulfill this objective, the galvanic currents flowing between the weld regions were recorded using parallel zero-resistance ammeters, and the self-corrosion rates of the couples were obtained by linear polarization resistance measurements.

The results showed that when 30 ppm of green oil field inhibitors were present in the service environment, a current reversal took place, resulting in accelerated weld corrosion. At high shear stress, the currents increased and further reversals occurred. The inhibitors were more effective in controlling the self-corrosion rates of the parent material than of the WM and HAZ material. It was concluded that PWC was caused by unstable conditions in which the inhibitor film was selectively disrupted from the WM and HAZ, but remained effective on the parent material.

Electrochemical corrosion rate measurements were carried out using an RCE produced from the different regions of the weld. An advantage of using the RCE is that the hydrodynamic conditions are very well defined, and it is feasible to translate the conditions that are known to exist in a production pipeline to those used in laboratory tests.

Corrosion inhibitors for copper immersed in emulsion were investigated by experiments and theoretical calculations, and this study aims to propose a new inhibition mechanism of the inhibitors having protective effects for copper corrosion.

Adsorption behavior of penta-heterocycles (thiophene, 1,2,5-oxadiazole, furan, 2 H-1,2,3-triazole, pyrrole and 1,2,5-thiadiazole) as corrosion inhibitors for copper immersed in oil-in-water (O/W) emulsions was investigated by weight loss, electrochemical tests, morphological characterization and theoretical calculations.

The orders of inhibition effect are furan < pyrrole < thiophene < 1,2,5-oxadiazole < 2H-1,2,3-triazole < 1,2,5-thiadiazole, and 1,2,5-thiadiazole at 0.5 mM has the best inhibition effect for copper immersed in emulsion. The results of scanning probe microscope, scanning electron microscope and electrochemical test show that a protective barrier can be formed on the surface of copper substrate with six corrosion inhibitors, thus effectively inhibiting the corrosion of copper mainly through chemisorption and following Langmuir’s adsorption isotherm.

Quantum chemical and molecular dynamic simulations demonstrate that all these compounds attached to Cu matrix with a flat-adsorption mode to prevent the emulsion corrode copper. Adsorbed inhibitors act as a barrier at Cu matrix to block corrosion and improve hydrophobicity.

The purpose of this investigation was to evaluate the protective ability of 2-amino-N-octadecylacetamide (AOA) and 2-amino-N-octadecyl-3-(4-hydroxyphenyl) propionamide (AOHP) as corrosion inhibitors for N80 steel in 15 per cent hydrochloric acid (HCl), which may find application as eco-friendly corrosion inhibitors in acidizing processes in the petroleum industry. Due to scale plugging in the well bore, there can be a decline in the crude production rate, and an acidization operation has to be carried out, normally by using 15 per cent HCl to remove the scale plugging. To reduce the aggressive attack of HCl on tubing and casing materials (N80 steel), inhibitors are added to the acid solution during the acidifying process.

Different concentrations of the synthesized inhibitors AOA and AOHP were added to the test solution (15 per cent HCl), and the corrosion inhibition efficiencies of these inhibitors for N80 steel were calculated from weight loss determinations, potentiodynamic polarization scans and alternating current (AC) impedance measurements. The influence of temperature (298-323 K) on the inhibition behavior was studied. Surface examinations were performed by means of Fourier transform infrared spectra and scanning electron microscope.

AOA and AOHP at 150-ppm concentration showed a maximum efficiency of 90.04 and 94.97 per cent, respectively, at 298 K in 15 per cent HCl solution. Both the inhibitors acted as mixed corrosion inhibitors. The adsorption of the corrosion inhibitors at the surface of the N80 steel was the underlying mechanism of corrosion inhibition.

This paper reports the preliminary laboratory results of inhibitors AOA and AOHP for the corrosion prevention of N80 steel casings and tubulars exposed to HCl and may be of practical help to petroleum engineers for carrying out acidization in oil wells after further investigation of the compound at higher temperature.

The purpose of this paper is to evaluate the corrosion inhibitor performance in acid medium through the determination of Fe2+ ions present based on reaction kinetics of steel with the acid. The use of corrosion inhibitors has been an excellent technique for protecting carbon steel pipes acidizing operations in oil wells. The inhibitor forms a chemical barrier on the metal surface that prevents or reduces attack by the acidic media.

The experimental study provides a methodology to evaluate the performance of corrosion inhibitors in an acid medium, preferentially of concentrated hydrochloric acid. The process consists essentially of total immersion coupons of carbon steel, with continuous stirring, controlled temperature and quantitative determinations of iron ions from the dissolution of steel. The additions of commercial corrosion inhibitor base of ethoxylated amines of high molecular weight in an acid medium showed excellent performance at a temperature ranging from 25 to 45°C.

This paper presents the mechanisms of protection, performance graphs and calculations of the activation energies of the addition of corrosion inhibitors in an acidic medium.

The originality of this essay is to evaluate and correlate the performance of corrosion inhibitors with the activation energy in experimental conditions.

The purpose of this paper was to find a simple and easy-operated method for filtering eco-friendly corrosion inhibitors.

The molecular structures and atomic electronegativities of the four kinds of natural reagents, iota-Carrageenan, sodium alginate, sodium dodecanesulphonate (SDS) and sodium dodecylbenzene sulfonate were calculated by Gaussian and Natural Bond Orbital, and the corrosion inhibition rates were forecasted by the calculated results. Then, the realistic corrosion inhibition efficiency were confirmed by electrochemical impedance spectroscopy and potentiodynamic polarization tests in 3.5 Wt.% sodium chloride corrosive solutions. At the same time, the function of pefloxacin mesylate (PM) was explored in this paper polarization tests in 3.5 Wt.% sodium chloride corrosive solutions.

Results showed that the order calculated by the chemical software was correct, and the corrosion inhibition of SDS was the best. Optimum addition of PM not only can reduce microbial corrosion but also can improve the corrosion inhibition by spatial cooperation.

This method can be used to filter eco-friendly corrosion inhibitors quickly. PM can be also used to improve the corrosion inhibition rate of corrosion inhibitors.

The present method to filter corrosion inhibitors was time-consuming, which needed lots of experiments to verify the corrosion inhibitive efficiency. The calculated method was simpler than others, which need complicated calculation process.

This study aims to investigate the effect of vapor phase corrosion inhibitor (VCI) imidazoline, quinoline and urea on E36 ship steel in simulated marine atmospheric environment.

The inhibitive effect was investigated by weight loss, potentiodynamic polarization, electrochemical impedance and Raman spectroscopy.

The corrosion process was inhibited by adsorption of the three VCIs on the surface of ship steel. The corrosion inhibition mechanism is the adsorption film type. The corrosion inhibitor adsorbs on the metal surface to prevent Cl^- from reaching the surface of the substrate, so as to achieve the corrosion inhibition effect.

To the best of the authors’ knowledge, the work described was original research that has not been published previously and not under consideration for publication elsewhere, in whole or in part.

The purpose of this paper is to understand corrosion behavior of copper and aluminum in monopropylene glycol-based heat transfer fluid by using synthetic and green inhibitors.

Weight loss, potentiodynamic and impedance measurements were applied to specimens to obtain their electrochemical characteristics and corrosion behaviors. Ageing test was applied to the fluids that contain different corrosion inhibitors to see the effect of inhibitors on fluid structure, and surface morphologies were examined by scanning electron microscopy (SEM).

The corrosion tests showed that synthetic inhibitors have better anti-corrosion potential than green inhibitors.

Like the synthetic corrosion inhibitors, there is growing interest in green inhibitors. Synthetic corrosion inhibitors are expensive and toxic for live beings, but green inhibitors from naturel sources are easy to reach and non-toxic for live beings and environment.

For solar heating systems, there is a need to select the correct heat transfer fluid; corrosion behavior of fluid plays a major role in the operation because the big part of the heating system consists of copper and aluminum close to ferrius metals and stainless steel.

The purpose of this paper is to make people aware of organic corrosion inhibitors.

As it is a literature review paper, no specific method is used.

It has been found that plant extracts and oils show inhibition efficiency up to 98 percent, so it is certain that plant extracts and oils are effective corrosion inhibitors and can be successfully used at the industrial level.

Plant extracts and oils are also found to be non‐toxic, highly efficient, renewable and cheap. But less effort has been given towards the identification of which compound is active in the extract.

The paper shows detailed account of the inhibitors obtained from plants, which are used as natural corrosion inhibitors.

The purpose of this study was to investigate the performances of three inhibitors in controlling corrosion of local mild steel products in distilled water and a simulated salt solution.

Corrosion inhibition of mild steel was investigated using electrochemical techniques. Untreated and inhibitor treated specimens were fully immersed in two test solutions, distilled water and the simulated solution of 2.0 wt.% NaCl and 1.0 wt.% Na2SO₄.

During full immersion in the simulated salt solution, sodium dihydrogen orthophosphate was not effective at all, resulting in even higher corrosion rates than that of the untreated specimens. Sodium benzoate was effective for three days only. Dicyclohexylamine nitrite was the most effective of them all, keeping its effectiveness for as much as 20 days. When the specimens were immersed in distilled water, all three inhibitors were effective during the 60 days of immersion while dicyclohexylamine nitrite and sodium benzoate treated specimens performed better than those treated with sodium dihydrogen orthophosphate.

The objective of this research was to investigate the performances of three inhibitors – sodium dihydrogen orthophosphate (inorganic) at 10 mM concentration, dicyclohexylamine nitrite (organic) and sodium benzoate (organic) at 100 mM concentration – in controlling the corrosion of local mild steel products fully immersed in two test solutions, distilled water and the simulated salt solution. All three inhibitors are film forming and anodic type inhibitors. According to the authors' literature review, this study is original and will add value to the studies of inhibition of steel corrosion under similar environments.

The purpose of this paper is to study the corrosion inhibition performance of an eco-friendly drug clozapine on the corrosion of copper in 1.0 M nitric acid and 0.5 M sulfuric acid solutions.

The corrosion inhibition nature of inhibitor molecule was evaluated by weight loss, electrochemical impedance spectroscopy and potentiodynamic polarization studies. An attempt was made to correlate the molecular properties of neutral and protonated forms of inhibitor molecule using quantum chemical calculations. The effect of temperature on the corrosion inhibition efficiency was also studied using electrochemical impedance spectroscopy. The potential of zero charge was determined to explain the mechanism of corrosion inhibition.

The studies on corrosion inhibition performance of clozapine showed that it has good corrosion inhibition efficiency on the corrosion of copper in 1.0 M nitric acid and 0.5 M sulfuric acid solutions. The adsorption of clozapine molecules onto the copper surface obeyed the Langmuir adsorption isotherm. The value of free energy of adsorption calculated is very close to −40 kJmol⁻¹, indicating that the adsorption is through electrostatic coulombic attraction and chemisorption. The decrease in the value of energy of activation with the addition of inhibitor also shows the chemisorption of the inhibitor on the metal surface. The potential of zero charge and quantum chemical studies confirmed that the protonated molecules also get involved in the corrosion inhibition process through physisorption.

The present work indicates that clozapine can act as a good corrosion inhibitor for the corrosion of copper in acid media.