淀粉接枝共聚物对Zn的缓蚀性能

以过硫酸铵-亚硫酸氢钠为引发剂,将丙烯酰胺单体接枝到淀粉上制备了淀粉接枝共聚物(St-g-PAM),可作为一种新型“绿色”缓蚀剂.通过失重实验和电化学测试研究了St-g-PAM对1.0 mol/L HCl溶液中Zn的缓蚀效果.结果 表明,St-g-PAM在HCl溶液中对Zn具有较好的缓蚀性,是一种混合抑制型缓蚀剂.缓蚀...     

Localized corrosion of copper alloys in China seawater for 16 years

The regulation of localized corrosion of 2 kinds of copper and 17 kinds of copper alloys exposed in seawater of Qingdao, Zhoushan, Yulin and Xiamen for 16 years has been studied. Results show that during immersion copper alloys suffer from pitting corrosion due to high temperature and marine living adhesion at Yulin, and to the higher velocity of seawater containing sand at Zhoushan. However, the seawater of Xiamen inhibits the pitting corrosion of copper alloys. No pitting corrosion is observed on copper alloy plates tested there. The copper alloys suffer from more serious pitting corrosion in the tide zone than that in the immersion zone at Qingdao after long time exposure.     

Inhibition of copper corrosion in acidic chloride pickling solutions by 5-(3-aminophenyl)-tetrazole as a corrosion inhibitor

Inhibition of copper corrosion in acidic chloride pickling (0.5 M HCl) solutions by 5-(3-Aminophenyl)-tetrazole (APT) as a corrosion inhibitor has been studied using potentiodynamic polarization, chronoamperometry (CA), electrochemical impedance spectroscopy (EIS), weight-loss and Raman spectroscopy investigations. Electrochemical measurements showed that the presence of APT and the increase of its concentration significantly decrease the cathodic, anodic, and corrosion currents as well as corrosion rates. This effect also decreases the dissolution currents of copper at 200 mV vs. Ag/AgCl, and greatly increases surface and polarization resistances and inhibition efficiency as indicated by CA and EIS measurements. Weight-loss data revealed that the corrosion rate of copper decreases to a minimum and the inhibition efficiency increases to a maximum in the presence of APT and upon increasing of its concentration even after 72 h of copper coupons immersion. Comparing the Raman spectrum obtained on the copper surface after its immersion in HCl solution containing 1.0 mM APT for 72 h to the spectrum obtained for the solid APT alone indicated that APT molecules inhibit the corrosion of copper via their adsorption onto its surface.     

Effects of alternating magnetic field on the corrosion rate and corrosion products of copper

The effects of alternating magnetic field on the corrosion morphologies, corrosion rate, and corrosion products of copper in 3.5% NaCl solution, sea water, and magnetized sea water were investigated using electrochemical test, scanning electron microscopy/energy dispersive analysis system of X-ray (SEM/EDAX), and X-ray diffraction (XRD). The results show that the corrosion rate of copper in magnetized sea water is minimal. Moreover, the surface of the specimen in magnetized sea water is uniform and compact as compared with those in 3.5% NaCl solution and sea water. The corrosion products of copper in magnetized sea water are mainly Cu2O and CuCl2. However, the corrosion products in sea water are CuCl, Cu2Cl(OH)3, and FeCl3·6H2O. The electrochemical corrosion mechanisms of copper in the three media were also discussed.     

Composite corrosion inhibitors for secondary alkaline zinc anodes

The corrosion inhibition property of PEG600 and In(OH)3 as composite corrosion inhibitors for secondary alkaline zinc electrodes was studied, and the inhibition efficiency was determined as 81.9%. The research focused on the mechanism by the methods of electrochemical impedance spectroscopy, polarization curves and IR spectroscopy. The results indicate that the corrosion inhibition effectiveness is attributed to the joint inhibition of anodic zinc dissolution and cathodic hydrogen evolution. And the anodic process is depressed to a greater extent than the cathodic process. The synergistic mechanism of the composite inhinbitors proves to be the enhancement of adsorption of PEG600 by In(OH)3. Potentiostatic experiment results and SEM images verify the inhibition of dendritic growth by the composite inhibitors.     

Inhibition of iron corrosion in acid solutions by Cefatrexyl: Behaviour near and at the corrosion potential

The corrosion inhibition of iron in HCl, HClO₄, H₂SO₄ and H₃PO₄ solutions (1M for each) by cefatrexyl has been studied by polarization resistance (R_p) and electrochemical impedance spectroscopy (EIS) at the corrosion potential. The results obtained at 30 °C revealed that cefatrexyl acts as a weak inhibitor in HCl solution while it shows excellent inhibition performance in the remaining acids. Adsorption of cefatrexyl in HCl solution obeys Langmuir’s isotherm with a very low value of the free energy of adsorption (physisorption) while its adsorption in the other acids follows Temkin’s isotherm with very high negative values of (chemisorption). Data obtained from EIS measurements were analyzed to model the corrosion inhibition process through appropriate equivalent circuit models. The calculated values of the apparent activation energy (E_a) and the pre-exponential factor (λ) indicate that cefatrexyl blocks nearly the whole active centers of iron surface in H₃PO₄ solution even at elevated temperatures. The inhibition mechanism of cefatrexyl was discussed.     

Inhibition of atmospheric corrosion of mild steel by sodium benzoate treatment

The objective of this study was to evaluate the effectiveness of sodium benzoate as an inhibitor to slow down or prevent atmospheric corrosion/discoloration of the local mild steel during storage in the Arabian Gulf region. Test specimens were prepared from locally produced reinforcing steel products. The inhibitor solution was applied on steel specimens at a concentration of 100 mM for 1 day at room temperature. Wooden exposure racks were used to hold as-received and inhibitor-treated specimens during atmospheric exposure for different periods. Corrosion was evaluated through weight loss determination and electrochemical technique. As expected, the Arabian Gulf atmosphere was corrosive on the as-received local mild steel. On the other hand, treatment of steel with sodium benzoate lowered its corrosion rate during initial days of its exposure to atmosphere. However, atmospheric corrosion inhibition performance of sodium benzoate deteriorated with exposure time after 30 or more days of atmospheric exposure, and the corrosion rates of sodium benzoate-treated specimens reached that of the unprotected specimens at the end of 90 days of atmospheric exposure.     

二氧化碳腐蚀缓蚀剂及其缓蚀机理的研究进展

首先分别论述了单组分缓蚀剂和复配型缓蚀剂的缓蚀机理,即不同类型的缓蚀剂在金属表面所具有的不同吸附过程。单组分缓蚀剂中特殊的分子基团在金属表面通过物理吸附、化学吸附或混合吸附过程起到缓蚀作用,复配型缓蚀剂在金属表面通过各组分间协同吸附或竞争吸附过程起到缓蚀作用,并指出了缓蚀机理的研究所存在的问题。然后,主要综述了近几年来国内外对用于二氧化碳腐蚀缓蚀剂的研究进展,包括咪唑啉衍生物、表面活性剂、季铵盐、有机胺和复配型缓蚀剂,结合缓蚀剂的分子结构和缓蚀效率等对其进行了阐述。介绍了几种用于二氧化碳腐蚀的新型缓蚀剂,如多活性位点有机化合物、硫醇、席夫碱和聚合物等。最后针对二氧化碳腐蚀环境的复杂性,对未来缓蚀剂及其缓蚀机理的研究方向进行了展望。     

Inhibition of copper corrosion by coatings of alkyl esters of carboxybenzotriazole

The inhibitive effect of coatings formed dipping copper in solutions of alkyl esters (methyl, butyl, hexyl and octyl) of carboxybenzotriazole was studied by potentiodynamic polarisation, electrical impedance spectroscopy, coulometry and surface enhanced Raman scattering (SERS) spectroscopy. The inhibition efficiency of the dry film depends on type of solvent used in the coating solution, temperature and period of immersion. Pretreatment by immersing copper in hot (70 °C) aqueous solution (1×10⁻⁴ M) for approximately 2-3 h gave a film with the highest degree of corrosion protection. Higher temperatures or longer time of immersion reduce the protectiveness of the film. Copper coated using either alcohol or acetone as solvent was less well protected than when dipped in aqueous solution. Impedance spectra showed that the film formed by pretreatment in aqueous solution of inhibitors can be stable in acidic sulphate corrodent (pH∼0) for up to 3 days before breaking down. In near-neutral sulphate solution (pH∼8) the film can be stable for up to 10 days. In both acidic and neutral sulphate solution, the inhibition efficiencies of the protective film increased with the length of the alkyl ester chain in the order: methyl < butyl < hexyl < octyl. This is different to the behaviour of copper in a near-neutral aqueous corrodent containing dissolved inhibitor. The ester films also exhibit anti-tarnishing properties in a sulphidising environment with inhibition efficiencies increasing as the alkyl chain is made longer. Again the films formed by pretreatment in aqueous solution have superior anti-corrosion properties compared to those formed by pretreatment in either alcohol or acetone solution. SERS measurements indicate that the azole ring is close to the copper surface with chemisorption through azole nitrogen. It is also suggested that the hydrocarbon chain of the ester is physically adsorbed on the copper.     

某热电厂凝汽器铜管腐蚀原因分析

河北南网某热电厂循环冷却水系统补水为地表水,检修时发现凝汽器中Hn70-1B铜管有腐蚀泄漏现象.通过现场检查发现腐蚀呈一定的规律性,通过试验分析结合现场检查情况判断总结该厂凝汽器铜管腐蚀成因,并针对这些腐蚀成因提出改进措施,保证机组的安全稳定运行.     

Inhibition of copper corrosion by silane coatings

OFHC copper specimens were pre-filmed in hydro-alcoholic solutions of various silanic agents (3-mercapto-propyl-trimethoxy-silane, PropS-SH; bis-triethoxy-silyl-ethane, BTSE; n-octadecyl-trimethoxy-silane, OctadecS; phenyl-trimethoxy-silane, PhS) to evaluate the influence of the silane molecule structure towards copper corrosion protection. Linear polarization resistance, potentiodynamic polarization curves, and electrochemical impedance spectroscopy tests were performed in 0.6 M NaCl.The thiolate bond caused a good anchoring of the silane molecule on the copper surface, which determined a noticeable hindrance to the anodic reaction of copper oxidation. Since this bond was found to be stronger than that of the oxane bond, the PropS-SH coating was more corrosion resistant and more persistent than the other tested silane coatings.The optimum pre-treatment solution pH was 4, although PropS-SH coating presented some imperfections. At this pH the coating was thicker than that at pH 10, when the silanized layer completely covered the copper surface. Nevertheless, the defects of this layer were so small that they could be plugged, for a prolonged time, by the copper corrosion products.     

Inhibition of stress corrosion cracking of alloy AA8090 T-8171 by addition of rare earth salts

Aluminium-lithium alloys are suitable for aeronautical purposes because of their good mechanical properties and high damage tolerance. Although these alloys are less susceptible to stress corrosion cracking than conventional alloys, Al-Li-Cu-Mg alloy (8090-T8171) still experiences this problem in a NaCl + H₂O₂ solution.In this work it has been demonstrated that the addition of 10,000 ppm of CeCl₃ to the medium inhibits the stress corrosion cracking of 8090 alloy by precipitation of cerium oxides/hydroxides. The deposition of these compounds on the alloy surface decreases the pit density and slows the crack growth through the grain boundaries by hindering the anodic dissolution of T phases.     

Analysis of corrosion resistance behavior of inhibitors in concrete using electrochemical techniques

Reinforced concrete is one of the most durable and cost effective construction materials. However, in high chloride environments, it can suffer from corrosion due to chloride induced breakdown of the normal passive layer protecting the reinforcing steel bars inside concrete. One means of protecting embedded steel reinforcement from chloride induced corrosion is the addition of corrosion inhibiting admixtures. In the present investigation, various inhibitors such as sodium nitrite, zinc oxide, mono ethanol amine, diethanolamine, and triethanol amine have been used in concrete in different percentages. Their effectiveness was then studied using various electrochemical techniques such as rapid chloride ion penetration test, open circuit potential measurement, electrochemical impedance measurement, potentiodynamic polarization measurement, and gravimetric weight loss measurement. The results thus obtained indicate that the addition of inhibitors enhances the corrosion resistance properties.     

Inhibition of copper corrosion in aerated hydrochloric acid solution by heterocyclic compounds containing a mercapto group

Inhibition of copper corrosion by benzotriazole (BTA), 2-mercapto benzoxazole (MBO) and 2-mercapto benzimidazole (MBI) in 0.5 mol L⁻¹ HCl was investigated by weight-loss measurements, potentiodynamic polarization curves and electrochemical impedance spectroscopy. MBI was shown to be the most effective inhibitor among those tested. Potentiodynamic polarization results revealed that the three compounds acted as anodic inhibitors, particularly MBI strongly suppressed anodic current densities. Molecular structure parameters of BTA, MBO and MBI were obtained by using an MM2 forcefield program and PPP–SCF quantum chemical calculation. It was found that MBI has higher levels of HOMO and LUMO energy and the larger π-electron density.     

Effect of temperature on copper corrosion in high-level nuclear waste environment

The effect of temperature on the corrosion behavior of copper in simulated high-level nuclear waste environment was systematically studied. Electrochemical methods, including electrochemical impendence spectra, Mott–Schottky technology, cyclic polarization, and potentiostatic polarization, were employed to characterize the corrosion behavior of copper at different temperatures. Stereoscopic microscopy and scanning electron microscopy were used to examine the surface morphology, and X-ray photoelectron spectroscopy analysis was used to identify the composition of the passive film. The experimental results show that corrosion resistance of the passive film does not blindly decrease with the increase of temperature but increases at 60 °C owing to a compact outer layer; there is a potential for pitting corrosion, which decreases as the temperature increases. The main product of copper in an anaerobic aqueous sulfide solution is Cu₂S but the content of CuS increases at higher temperatures. The whole passivation range shows p-type semiconductor characteristics and the magnitude of the acceptor density is 10²³ cm^?3, which increases with increasing temperature.     

The use of quantum chemical methods in corrosion inhibitor studies

Quantum chemical methods are particularly significant in the study of electrochemistry and provide researchers with a relatively quick way of studying the structure and behaviour of corrosion inhibitors. The originality of this review article is based on the fact that it is the first and unique general reference for all those interested in the use of quantum chemical methods in corrosion inhibitor studies. It begins with a concise summary of the most used quantum chemical parameters and methods and then summarizes the results of research articles in corrosion science over the past 20 years.     

两种曼尼希碱缓蚀剂的缓蚀性能

采用甲醛/苯甲醛、苯乙酮和水合肼为原料分别合成了AJ和BJ两种曼尼希碱缓蚀剂。通过静态挂片失重法、电化学测试法等方法研究了在15%HCl(质量分数)溶液中,这两种缓蚀剂对N80钢的缓蚀性能。结果表明:在15%的HCl溶液中,AJ和BJ缓蚀剂对N80钢具有良好的缓蚀作用,且BJ缓蚀剂的缓蚀效果要优于AJ缓蚀剂的;两种缓蚀剂均为阳极型缓蚀剂,都能自发吸附在N80钢表面,其行为均符合Langmuir吸附等温式。     

Correlation of temperature with galvanic corrosion behaviour of copper alloys based on wire beam electrode

Galvanic corrosion behaviour of copper and copper alloys in chloride solution (0.6?M NaCl) under different temperature conditions (35°C, 55°C and 80°C) was investigated by the wire beam electrode (WBE) method. It was found that the average galvanic current of the Cu and Cu–Sn alloy, which shifted from the cathode at 35°C to the anode at 80°C, increased as temperature increased during the immersion time. In contrast, the average galvanic current of Cu–Zn alloy can be ranked as 35°C?>?55°C?>?80°C. A sudden conversion was that the anode average current of Cu–Zn alloy at 35, 55°C changed into the cathode when the immersion time lasted untill 3 h at 80°C. The results indicate that it is feasible to study the corrosion behaviour under the different temperature environment with the WBE method.     

Cu/Ti在模拟海水中的电偶腐蚀行为(英文)

采用电化学阻抗谱、电化学噪声和扫描电镜等技术研究了纯铜、铜/钛耦合电极在模拟海水中的腐蚀行为。结果表明:纯铜的腐蚀过程分2个阶段,其腐蚀阻抗和点蚀参数SE均遵循先增后降的规律,而其腐蚀参数SG的变化规律则正好相反;铜/钛耦合电极的腐蚀过程则由3个阶段组成,其腐蚀阻抗和点蚀参数SE均遵循先降后升到最后再降的规律,而其腐蚀参数SG则同样反向变化。铜和钛之间的电势差加速了纯铜的点蚀萌生,同时铜/钛耦合电极的腐蚀电位总是正于纯铜的腐蚀电位。