Corrosion Inhibition Mechanism Research Articles

Gleditsia sinensic extract as green corrosion inhibitor for N80 steel in 1 M HCl

The inhibition efficiency of gleditsia sinensic extract (GSE) as green corrosion inhibitor for N80 steel has been evaluated by weightlessness test, electrochemical impedance spectroscopy (EIS) study, Potentiodynamic polarization (PDP) measurement and Density Functional Theory (DFT) calculations in 1M HCl solution. Consequently, the inhibition efficiency of GSE is increased with the concentrations, immersion time and corrosion temperature (except 60 °C). After 144 h of immersion at 30 °C, the inhibition efficiency of GSE at a concentration of 500 mg/L was as high as 92.34 %. The adsorption process was spontaneous exothermic and conformed to Langmuir's law of adsorption, while Tafel's analysis showed that GSE is a mixed type of inhibitor. In addition, the corrosion products have been examined by scanning electron microscopy (SEM) analysis, X-Ray Diffractomer (XRD) testing, Fourier transform infrared spectroscopy (FTIR-ATR), UV-Vis spectroscopy and contact angle (CA) measurements. Furthermore, the corrosion inhibition mechanism has also been investigated.

Strain effects on corrosion inhibition in stress corrosion of tubing steel

In this investigation, we explored the corrosion inhibition mechanism of an imidazoline quaternary ammonium salt (IQA) on J55 steel in simulated annulus environment through a series of experiments, including electrochemical testing, stress corrosion immersion experiments, and hydrogen permeation testing. Our findings reveal that IQA functions as a mixed-type inhibitor, exerting its inhibitory action through chemical adsorption. Notably, it exhibits a stronger inhibitory effect on the anodic dissolution reaction compared to the cathodic hydrogen evolution reaction. Despite the minor influence of tensile plastic strain on the average inhibition efficiency, it notably exacerbates pitting and initiates stress corrosion cracking. This underscores the limitation of average inhibition efficiency in accurately assessing IQA's efficacy against stress corrosion. Additionally, hydrogen permeation experiments and electrochemical testing demonstrate that plastic strain diminishes IQA's inhibitory effect on the cathodic hydrogen evolution reaction, facilitating hydrogen diffusion into the steel substrate and thereby exacerbating stress corrosion in J55 steel. Consequently, at low IQA inhibitor concentrations (as in this study, 12.5 mg L−1), despite high average inhibition efficiency, it proves ineffective in mitigating stress corrosion.

Experimental and theoretical computational study of corrosion inhibitors in the cobalt bulk chemical mechanical polishing (CMP) process

Cobalt is a potential substitute for copper as local interconnects in sub-10 nm interconnects, the chemical mechanical polishing (CMP) of which is quite challenging due to the high chemical reactivity of Co. By using a combination of experiments and theoretical calculations, the optimum corrosion inhibitor of Co is identified and the corrosion inhibition mechanism of TTLYK on Co is further investigated. It investigates the effects of various corrosion inhibitors, including potassium oleate, dodecyl benzene sulphonic acid, octyl hydroxamic acid, and 2,2′-[[(methyl-1H-benzotriazol-1yl) methyl] imino] bis-ethanol (TTLYK) on Co through chemical mechanical polishing and static etching experiments. The results show that among various corrosion inhibitors, TTLYK presents the best corrosion inhibition effect. When the basic slurry contains 10 mM TTLYK, the corrosion inhibition efficiency could reach 96.23 %, the material removal rates of Co is 161.79 nm/min, the static etching rates is 0.85 nm/min, and the material removal selectivity ratio of Co and Ti is 39:1. The results fully meet the requirements of the Co bulk CMP process. It is revealed TTLYK could form a protective layer with a synergistic physical and chemical adsorption on Co, in which the chemical adsorption occurs through the formation of CoN bonds. The adsorption of TTLYK could decelerate the transformation of CoO and Co(OH)2 to Co3O4, and the as formed Co-TTLYK complex provides the main corrosion inhibition.

Insights into the newly synthesized bi- Mannich base for carbon steel corrosion inhibition in H2S and HCl solution

Adding corrosion inhibitors is considered to be a cost-effective way to inhibit metal corrosion. In this study, we report the synthesis of a bi-mannich base corrosion inhibitor (BMT) with an impressive inhibition efficiency on carbon steel in H2S and HCl co-existing solution. At the BMT concentration of 9 ppm, the inhibition efficiency (η) of 96.9%, 97.6% and 98.0% were determined by weight loss, potentiodynamic polarization and electrochemical impedance spectroscopy, respectively. The adsorption of BMT on the carbon steel surface follows the Langmuir adsorption isotherm, and the calculated free energy indicates that the adsorption is a spontaneous process. This research also delves into understanding the adsorption behavior and corrosion inhibition mechanism of BMT on carbon steel surfaces through quantum chemistry calculations. The results of this study provide guidance for the application of BMT as a corrosion inhibitor in sour and acid environments.

In-depth study of a newly synthesized imidazole derivative as an eco-friendly corrosion inhibitor for mild steel in 1 M HCl: Theoretical, electrochemical, and surface analysis perspectives

The present study is concerned with the corrosion inhibition and adsorption behaviour of a series of novel imidazole derivatives. The compounds under investigation are 5,5-diphenyl-3-propyl-2-(propylthio)-3,5-dihydro-4 H-imidazol-4-one (AM3) and 3-allyl-2-(allylthio)-5,5-diphenyl-3,5-dihydro-4 H-imidazol-4-one (AM6). The objective of this study is to evaluate the efficacy of 5,5-diphenyl-3,5-dihydro-4 H-imidazol-4-one (AM6) as a corrosion inhibitor on mild steel immersed in a 1.0 M hydrochloric acid medium. This comprehensive study assesses the efficacy of these derivatives through a range of electrochemical and spectroscopic analysis techniques. Additionally, polarisation curves, electrochemical impedance spectroscopy and advanced computer simulations were employed to evaluate the efficacy and inhibition mechanism of imidazole derivatives, thereby facilitating a more profound understanding of their anticorrosive capacity. The results obtained from potentiodynamic polarisation (PDP), electrochemical frequency modulation (EFM) and electrochemical impedance spectroscopy (EIS) measurements demonstrate that the inhibition efficiency increases with increasing imidazole derivative concentration. Conversely, an inverse relationship is observed between inhibition efficiency and temperature. The thermodynamic parameters ΔG°_ads and ΔH°_ads corroborate the conclusion that the adsorption process is predominantly chemical in nature. Scanning electron microscopy (SEM), energy dispersive X-ray spectroscopy (EDX) and X-ray photoelectron spectroscopy (XPS) were employed to characterise the surface morphology. The maximum protection afforded by imidazole derivatives was 95.2 % and 93 % for compounds AM3 and AM6, respectively. Polarisation curves indicated that imidazole derivatives exhibited mixed inhibition behaviour. Surface analysis demonstrated that imidazole derivatives were effectively adsorbed onto the carbon surface, thereby significantly reducing acid damage. This finding was corroborated by DFT calculations, as well as Monte Carlo (MC) and molecular dynamics (MD) simulations. These simulations provided a comprehensive insight into the adsorption of imidazole and its protonated form onto the carbon surface, offering valuable insight into the corrosion inhibition mechanism.

Corrosion inhibition performance and mechanism of triethanolamine-triisopropanolamine rust inhibitor in the simulated concrete pore solution

In this research, aiming to deal with the accelerated corrosion deterioration of steel reinforcement in reinforced concrete in harsh environments, a highly efficient rust inhibitor (triethanolamine (TEA)-triisopropanolamine (TIPA)) (abbreviated as TT), which TEA and TIPA compounded in a ratio 4:6, was proposed. The synergistic rust inhibition effect of TEA and TIPA on steel in the simulated concrete pore solution (SCPS), and its corrosion inhibition performance were investigated by electrochemical impedance spectroscopy (EIS), potentiodynamic polarization (PDP), dry and wet cycling, and scanning electron microscopy (SEM) measurements. The results showed that TT inhibitor could obviously inhibit the corrosion of steel in the SCPS and could inhibit both cathode and anode. The electrochemical corrosion inhibition performance was the most excellent at the dosage of 1.0 %, and the maximum corrosion inhibition efficiency (η1) reached 95.39 %. After 150 times of dry and wet cycling, the percentage of the corrosion area (S), and corrosion inhibition efficiency (η2) with 1.0 % TT inhibitor were 9.3 % and 84.03 %, respectively, and the mass loss rate (M) decreased by 68.4 %, indicating a better rust inhibition performance. The adsorption of the TT inhibitor conformed to the Langmuir adsorption isotherm and inhibited the corrosion of steel by forming a protective film on steel surface through physicochemical adsorption. This study is of great significance to provide new perspectives and improvement measures to build up the deterioration and extend the service life of reinforced concrete in harsh environments.

Carbon Dots for Anti‐Corrosion

AbstractCarbon dots (CDs) have garnered extensive attention owing to their excellent biocompatibility, elevated specific surface area, and facile functionalization, as well as their diverse methods of preparation. In recent times, CDs have been applied for anti‐corrosion and obtained some significant results. In this work, the preparation methods of CDs are first briefly introduced, and the relative merits of different approaches are highlighted. Subsequently, the application of CDs in the realm of corrosion inhibitors is discussed, and the corrosion inhibition effects and mechanism of nitrogen‐doped CDs, nitrogen and sulfur‐co‐doped CDs, as well as CDs functionalized with other elements and nitrogen‐co‐doped are summarized. Finally, the application of CDs and functionalized CD‐modified coatings for anti‐corrosion and their protective mechanism is analyzed in detail. This review summarizes recent progress in research related to CDs and heteroatom‐doped CDs in anti‐corrosion applications and anticipates the prospects and applications of CDs in corrosion protection. With their unique properties and versatile applications, CDs are expected to assume a progressively pivotal role in the advancement of cutting‐edge corrosion protection technologies.

Enhancement of wear and corrosion resistance of pulsed electrodeposited Ni–Mo amorphous/nanocrystalline coatings by heat treatment

In this study, Ni–Mo coatings with various sodium molybdate concentrations were designed and successfully electrodeposited. The effects of treatment with different temperatures (200 °C,400 °C, 600 °C) on the microstructure and properties of the best-performing coating (4 g/L) were investigated. The surface morphologies, elemental content, and phase structure of the prepared coatings were obtained and analyzed by SEM, EDS, XRD, WFI and TEM. The Ni–Mo coating after heat treatment at 400 °C formed the compact and uniform amorphous/nanocrystalline coating. As shown by the electrochemical and wear test. Heat treatment at 400 °C improved the coating properties, and the corrosion current density was decreased by 66 % to 6.2532 × 10−7 A/cm2. The wear rate reduced from 8.3 × 10−4 mm3/N·m to 3.6 × 10−4 mm3/N·m, and the average friction coefficient minimized to 0.079. Additionally, compared with the as-deposited coating, the microhardness reaches the maximum (1048 HV). The formation of the oxide layer and the intermetallic compound MoNi on the surface of the coating plays a carrying and hindering role, thus the surface of the coating shows excellent wear and corrosion resistance. In addition, the corrosion inhibition mechanism during the heat treatment of Ni–Mo coatings was further explored.

Green Corrosion Inhibitors for Metal and Alloys Protection in Contact with Aqueous Saline.

Corrosion is an inevitable and persistent issue that affects various metallic infrastructures, leading to significant economic losses and safety concerns, particularly in areas near or in contact with saline solutions such as seawater. Green corrosion inhibitors are compounds derived from natural sources that are biodegradable in various environments, offering a promising alternative to their conventional counterparts. Despite their potential, green corrosion inhibitors still face several limitations and challenges when exposed to NaCl environments. This comprehensive review delves into these limitations and associated challenges, shedding light on the progress made in addressing these issues and potential future developments as tools in corrosion management. Explicitly the following aspects are covered: (1) attributes of corrosion inhibitors, (2) general corrosion mechanism, (3) mechanism of corrosion inhibition in NaCl, (4) typical electrochemical and surface characterization techniques, (5) theoretical simulations by Density Functional Theory, and (6) corrosion testing standards and general guidelines for corrosion inhibitor selection. This review is expected to advance the knowledge of green corrosion inhibitors and promote further research and applications.

Study on the Performance and Mechanism of Morpholine Salt Volatile Corrosion Inhibitors on Carbon Steel

A series of morpholine salt volatile corrosion inhibitors (VCIs) were synthesized via solid-phase chemical reactions. The corrosion inhibition performance was assessed using evaporation weight loss, VCI capability, and corrosion weight loss tests. The corrosion inhibition mechanisms of the morpholine salt VCIs for carbon steel in atmospheric conditions were explored through electrochemical testing under thin film electrolytes, X-ray photoelectron spectroscopy (XPS), and computational simulations. Morpholine carbonate exhibited higher volatility. Corrosion weight loss tests showed an >85% reduction for steel treated with morpholine benzoate or morpholine carbonate. The inhibitors’ inhibition mechanism, elucidated through X-ray photoelectron spectroscopy (XPS) and computational simulations, revealed that morpholine carbonate and benzoate form protective layers via physical and chemical adsorption on the steel surface, coordinating with iron atoms through nitrogen and oxygen atoms. Quantum chemical calculations demonstrated that morpholine carbonate had stronger adsorption energy and electron transfer capabilities, indicating superior corrosion inhibition performance over morpholine benzoate.

N, S-carbon quantum dots as inhibitor in pickling process of heat exchangers for enhanced performance in multi-stage flash seawater desalination

The heat exchanger in multi-stage flash seawater desalination needs to be pickled during long-term service to remove oxidation products on the copper surface. In this paper, we introduce a method for preparing carbon quantum dots from biowaste, and explore their ability to inhibit the corrosion of copper in sulfuric acid and its corrosion inhibition mechanism. Firstly, the UV–vis spectra, microstructure, tissue composition of N, S-CDs were tested by Ultraviolet-visible spectrophotometer, TEM and Fourier transform infrared. Secondly, the effectiveness of N, S-CDs in preventing corrosion was analyzed by electrochemical testing. The electrochemical test results showed that the impedance value of the solution of 200 mg/L N, S-CDs was 94,440 Ω cm2 at 298 K， with corrosion inhibition efficiencies (η) of 99.89 %, 99.77 % and 99.72 % at 298 K, 308 K, and 318 K, respectively. Moreover, SEM, XPS and AFM were used to characterize the micro-morphology and composition both before and after corrosion. It is worth noting that we used the fluorescence properties of carbon quantum dots as fluorescent probes to deeply verify the corrosion inhibition mechanism of N, S-CDs on copper.

A purine derivative for the modulation of the corrosion behavior of nickel aluminum bronze in seawater: a comprehensive and in-depth investigation on the corrosion inhibition mechanism

6-mercaptopurine (SMP), recognized for its biological activity, is investigated for its corrosion inhibition mechanism on nickel-aluminum bronze (NAB) in seawater, demonstrating a high efficiency of 99.6%. The physical adsorption of SMP on the NAB surface contributes to the multilayer structural arrangement of SMP. The Cu+-SMP complex is generated on the surface of NAB, which possesses a corrosion protection effect. SMP alters the semiconductor properties of corrosion product layer and reduces the carrier concentration. SMP can adsorb better on uncorroded NAB surfaces. This study holds significant importance in unraveling the mechanisms behind the corrosion behavior of NAB surfaces regulated by SMP.

Synthesis, characterization, theoretical, and experimental evaluation of novel imidazolone − based compounds as eco-friendly corrosion inhibitors for mild steel

This study investigates the corrosion inhibition properties of two newly synthesized namely (E)-2-(2-benzylidenehydrazineyl)-5,5-diphenyl-3,5-dihydro-4H-imidazol-4-one denoted Ph-DDI and (E)-2-(2-(4-methylbenzylidene)hydrazineyl)-5,5-diphenyl-3,5-dihydro-4H-imidazol-4-one denoted CH3Ph-DDI, on mild steel (MS) in a 1 M HCl solution. These compounds demonstrated high inhibition efficiencies of 98.3 % and 98.7 %, respectively. Structural characterization was performed using FT-IR, 1H NMR, 13C NMR, and HRMS-ESI. Theoretical evaluations indicated high reactivity and potent inhibition capacity. Electrochemical tests confirmed a concentration-dependent inhibition effectiveness up to 328 K. Adsorption studies suggested that the compounds displace water molecules to form an adsorbed protective layer. Microscopy analysis provided insights into the corrosion inhibition mechanisms, confirming the formation of protective layers and iron/inhibitor complexes. Further molecular structure analysis using Monte Carlo (MC) simulations and density functional theory (DFT) calculations elucidated the structural features contributing to the compounds’ effective corrosion inhibition properties.

Sodium humate as green corrosion inhibition for enhanced corrosion resistance of EH40 ship plate steel

A new green corrosion inhibitor was extracted and prepared from available and inexpensive natural humic plant humus for the corrosion inhibition of EH40 steel in a 15 % HCl medium. The corrosion inhibition properties of SH were evaluated using weight loss, cyclic voltammetry, potentiodynamic polarization and electrochemical impedance spectroscopy. The morphology of EH40 steel was characterized using scanning electron microscopy, atomic force spectroscopy and x-ray photoelectron spectroscopy. It was found that, the optimum concentration of sodium humate was 1.0 gL−1 with an inhibition efficiency of above 95 %. The corresponding corrosion inhibition mechanism was proposed, in which the corrosion inhibitor formed a film on the surface of EH40 steel as a result of the synergistic adsorption effect of chemistry and physics, improving its corrosion retention in the strong acid medium.

Synthesis, crystal structure, theoretical calculations, and corrosion study of thiazine[1,5]benzodiazepine

A derivative of 1,5-benzodiazepine, specifically 2-methyl-6-phenyl-2,3-dihydro-1H-[1,3]thiazino[3,2-a]-1,5-benzodiazepin-1-one (TBD), was synthesized by a cyclization [3 + 3] reaction involving the 4-phenyl-1,3-dihydro-2H-1,5-benzodiazepine-2-thione and methacryloylchloride. The structure of TBD was characterized through various spectroscopic methods, including FT-IR, 1H NMR, 13C NMR, and HRMS, also it was confirmed by X-ray analysis. The corrosion inhibitory effectiveness of TBD for mild steel (MS) in 1 M HCl acid was inspected by the exploitation of electrochemical impedance spectroscopy (EIS) and potentiodynamic techniques. Monte Carlo (MC) simulations were employed to study the adsorption behavior of TBD on the Fe (110) surface, providing insights into its inhibitory efficiency against MS corrosion. The simulations were also utilized to calculate the energy of adsorption of the inhibitor onto MS. A comprehensive theoretical investigation, employing density functional theory (DFT) at the B3LYP/6–311 G (d,p) level, was carried out to validate the experimental findings regarding the inhibition properties of the synthesized product and to elucidate the corrosion inhibition mechanism.

Novel self-healing glass-like CexOY film on a Flash-PEO coated AZ31B Mg alloy

The aim of this work is to develop a glass-like CexOy coating to seal the pores of a Flash-PEO coated AZ31B Mg alloy and simultaneously provide smart self-healing corrosion protection. The cerium sol was synthesized using cerium acetate as main precursor by sol-gel method. SEM micrographs revealed that upon cerium sol deposition, the pores of the oxide coating were effectively sealed, resulting in a double-layer coating system and thereby in a big reservoir of cerium ions (Ce3+/Ce4+). The glassy character of the cerium coating, confirmed by X-Ray diffraction, implies that cerium exists in Ce3+ and Ce4+ ionic states enclosed in a high internal energy structure which facilitate the diffusion of cerium ions to active cathodic zone. Electrochemical Impedance Spectroscopy (EIS), X-Ray Diffraction (XRD), and Raman spectroscopy were used to explore the active corrosion protection of the CexOy sol-gel coating. The corrosion inhibition mechanism involves the migration of cerium ions and the precipitation of insoluble-crystalline cerium compounds (CeO2). The coating demonstrated self-healing properties, presenting a promising alternative to traditional chrome conversion coatings (CCC).

Investigating the efficacy of phenolic Schiff bases as corrosion inhibitors for mild steel in acidic environments: Integrating experimental and theoretical approaches (Part B)

Our research employs a holistic methodology to assess the efficacy of a series of phenolic Schiff bases as corrosion inhibitors for mild steel in a 1 M HCl solution. Through complementary studies, we aim to unravel the corrosion inhibition mechanism by investigating neutral, protonated, and complex forms of inhibitors using advanced computational and statistical methods. This initial investigation specifically involves evaluating the effectiveness of two phenolic Schiff bases through weight loss tests (WL) and electrochemical techniques. The study focuses on the corrosion inhibitory properties of two phenolic Schiff bases, namely 4,4′-((1E,1′E)-(ethane-1,2-diylbis(azaneylylidene))bis(methaneylylidene))diphenol (PSB7) and (1E,1′E)-N,N'-(ethane-1,2-diyl)bis(1-(4-nitrophenyl)methanimine) (PSB8), on mild steel (MS). Results from weight loss and electrochemical methods indicate that inhibition efficiency improves with decreasing temperature and increasing inhibitor concentration, reaching 94 % (for PSB7) and 93 % (for PSB8) at 303 K and 1 × 10−3 M, respectively. Consequently, both PSB7 and PSB8 function effectively as inhibitors in a mixed form. The adherence of both inhibitors to the surface follows the Langmuir adsorption isotherm model. Additionally, SEM and EDS experiments provide evidence of adsorption on the surface. The findings from Density Functional Theory (DFT) and Molecular Dynamic Simulations (MDS) consistently match the actual data, maintaining the order of inhibition efficiency (PSB7 > PSB8).

Research on the corrosion inhibition performance and mechanism of pyrimidine quaternary ammonium salt

PurposeAt present, research on the preparation of corrosion inhibitors using modified pyrimidine derivatives is still blank. The purpose of this study is to synthesize a new cationic mercaptopyrimidine derivative quaternary ammonium salt, known as DTEBTAC, that can be used as a corrosion inhibitor to slow down the metal corrosion problems encountered in oil and gas extraction processes.Design/methodology/approachA new corrosion inhibitor was synthesized by the reaction of anti-Markovnikov addition and nucleophilic substitution. The weight loss method was used to study the corrosion inhibition characteristics of synthetic corrosion inhibitors. Electrochemical and surface topography analyses were used to determine the type of inhibitor and the adsorption state formed on the surface of N80 steel. Molecular dynamics simulations and quantum chemistry calculations were used to investigate the synthetic corrosion inhibitor’s molecular structure and corrosion inhibition mechanisms.FindingsThe results of the weight loss method show that when the dosage of DTEBTAC is 1%, the corrosion rate of N80 steel in hydrochloric acid solution at 90? is 3.3325 g m-2 h-1. Electrochemical and surface morphology analysis show that DTEBTAC can form a protective layer on the surface of N80 steel, and is a hybrid corrosion inhibitor that can inhibit the main anode. Quantum chemical parameter calculation shows that DTEBTAC has a better corrosion inhibition effect than DTP. The molecular dynamics simulation results show that DTEBTAC has stronger binding energy than DTP, and forms a network packing structure through hydrogen bonding, and the adsorption stability is enhanced.Originality/valueA novel cationic mercaptopyrimidine derivative quaternium-ammonium salt corrosion inhibitor was designed and provided. Compared with the prior art, the preparation method of the synthesized mercaptopyrimidine derivative quaternary ammonium salt corrosion inhibitor is simple, and the presence of nitrogen-positive ions, sulfur atoms and nitrogen-rich atoms has an obvious corrosion inhibition effect, which can be used to inhibit metal corrosion during oil and gas field exploitation. It not only expands the application field of new materials but also provides a new idea for the research and development of new corrosion inhibitors.

The corrosion inhibition performance and mechanism of α-benzoin oxime on copper: A comprehensive study of experiments and DFT calculations

Copper corrosion poses a significant challenge to process stability and chip quality in the field of integrated circuit manufacturing. This study comprehensively explored the corrosion inhibition performance of α-benzoin oxime (bzoxH2) on copper, by employing a combination of experimental methods and computational chemistry. First, after the addition of 0.1 mM bzoxH2, the static etching rate and surface roughness of copper were decreased to 7 Å·min−1 and 1.36 nm, respectively, which indicated that bzoxH2 could reduce the corrosion rate of copper and improve its surface quality. Subsequently, electrochemical behavior analysis showed that the addition of 0.1 mM bzoxH2 resulted in an increase in open circuit potential to 0.185 V, a decrease in corrosion current density to 2.33 µA·cm−2, an increase in polarization resistance to 10589 Ω·cm2, and a high corrosion inhibition efficiency of 96.88 %, suggesting that bzoxH2 significantly enhances the corrosion resistance of copper. Furthermore, studies based on adsorption isotherm models indicated that the adsorption behavior of bzoxH2 on the copper surface formed a dense passivation film through the combination of physical and chemical adsorption mechanisms. This effectively enhanced the corrosion resistance of copper and provided robust protection against corrosion. Finally, the use of X-ray photoelectron spectroscopy technology, along with an in-depth exploration of the geometric structure and chemical reactivity of the bzoxH2 molecule, revealed its complex interaction with specific active sites on the copper surface. These findings provided valuable theoretical insights, along with practical guidance for the development of metal corrosion inhibitors.

Corrosion inhibition, long-term and adsorption mechanisms of humic acid on ADC12 aluminum alloy in oxalic acid solution

Corrosion inhibition, long-term and adsorption mechanisms of humic acid on ADC12 aluminum alloy in oxalic acid solution