Nanocap-shaped tin phthalocyanines: synthesis, characterization, and corrosion inhibition activity

Thermal and microwave reactions between [PcSn(IV)Cl2] (1) and the potassium salts of eight fatty acids (2 a-h) led to cis-[(RCO2)2Sn(IV)Pc] compounds (3 a-h) in yields ranging from 54 to 90 %. Compounds 3 a-h were fully characterized by elemental analysis, spectroscopy (IR, UV/Vis, multinuclear NMR), and seven X-ray diffraction structures, whereby two different allotropes were observed in two cases. The two carboxylates in 3 have a cis anisobidentate binding mode, octacoordination of the tin atoms with square-antiprismatic geometry, and pi-electron-rich nanocap shapes. On account of the latter characteristics, 3 a-h compounds have anticorrosion properties. LPR and Tafel electrochemical methods were used to characterize the behavior of these derivatives in naturally aerated sour brine, which is a common environment in petroleum production and refinery operations. The measurement of the corrosion rate of carbon steel AISI 1018 in the presence of 3 a-h (500 ppm) gave efficiencies of 61-87 % for the inhibitor performance. Of the different derivatives examined, compounds 3 e and 3 h were the most effective corrosion inhibitor prototypes.     

不同聚合度聚乙二醇对A30碳钢的缓蚀性能

通过开路电位测量法、动电位极化曲线法和电化学阻抗谱法研究了表面活性剂聚乙二醇对A30碳钢的缓蚀作用,初步推测了其缓蚀机理．分别选取聚合度为600、2000、4000、6000的四种聚乙二醇进行实验,结果表明,聚乙二醇对碳钢的最高缓蚀率接近90％．聚乙二醇分子量对缓蚀作用有明显影响,相同浓度时聚合度越大,缓蚀性能越强．三种方法得到的结果具有同一性．     

The inhibiting effect of cobalt(III)–<Emphasis Type="Italic">cyclam</Emphasis> complexes with substituted β-diketones on iron corrosion in perchlorate solution

The inhibiting effect of cobalt(III) complexes with macrocyclic ligand cyclam (1,4,8,11-tetraazacyclotetradecane) and β-diketonato ligands have been investigated on iron corrosion in 0.1 M HClO₄ by potentiodynamic, linear polarization resistance (LPR), and electrochemical impedance spectroscopy (EIS) measurements. Analysis of the polarization curves and impedance spectra, by adding complex compounds to the acid solution and comparing with inhibitor-free solution, show corrosion current decrease and charge transfer resistance increase, respectively. Impedance data are fitted with equivalent circuit models. The stability of the adsorbed film was followed by LPR. Scanning electron microscopy (SEM) was used to screen physical changes of the reacted surfaces both treated and untreated. The differences in inhibitor efficiencies depend on the substituent group of the coordinated β-diketone ligand. Structural and electronic properties of this group of compounds in relation to inhibitor efficiency were analyzed by using the molecular modeling structures and correlated with previously reported spectroscopy data.     

Investigation of naphthyridines. VII. Synthesis of 10-alkylamino-1,2,3,4-tetrahydrobenzo[b]-1,6-naphthyridines

10-Alkylamino-2-methy1-1,2,3,4-tetrahydrobenzo[b]-1,6-naphthyridines were obtained by cyclization of alkylamides of N-(1-methyl-4-piperidylidene)anthranilic acids and also by reaction of 10-chloro-2-methyl-1,2,3,4-tetrahydrobenzo-[b]-1,6-naphthyridines with amine hydrochlorides.See [1] for communication VI.Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 2, pp. 263–265, February, 1976.     

Schiff’s bases as inhibitors of mild steel corrosion in hydrochloric acid

Mass loss and thermometric methods are used to study the inhibition of corrosion of mild steel in hydrochloric acid by Schiff’s bases N-(furfurlidine)-4-methoxy aniline, N-(furfurlidine)-4-methylaniline, N-(salicylidine)-4-methoxy aniline, N-(cinnamalidine)-4-methoxy aniline, and N-(cinnamalidine)-2-methylaniline. Results of inhibition efficiency yielded by the two methods are in good agreement and depend on the inhibitor and acid concentration. Maximum inhibition efficiency is 98%. The efficiency increases with the inhibitor concentration and acid strength. Published in Russian in Elektrokhimiya, 2007, Vol. 43, No. 2, pp. 252–256. The text was submitted by the authors in English.     

Influence of Molecular Weight on Mild Steel Corrosion Inhibition Effect by Polyvinyl Alcohol in Hydrochloric Acid Solution

The corrosion inhibition of mild steel in hydrochloric acid solution in the presence of three different molecular weights of polyvinyl alcohol (PVA) designated as PVA-I, PVA-II, and PVA-III corresponding to 14,000, 72,000, and 125,000 g mol^?1, respectively, was investigated using electrochemical impedance spectroscopy, linear polarization resistance (LPR), and potentiodynamic polarization techniques at 25°C. It was found that PVA of different molecular weights inhibited the corrosion of mild steel in the acid environment. Inhibition efficiency (η%) increases with increase in concentration of the polymers. LPR measurements clearly show that inhibition efficiency increases with increasing molecular weight in the order PVA-III > PVA-II > PVA-I. Polarization curves indicate that PVA functions as a mixed inhibitor affecting both the anodic metal dissolution and cathodic hydrogen evolution partial reactions of the corrosion process. The experimental data obtained fitted well into Langmuir adsorption isotherm model. Physical adsorption mechanism is proposed from the thermodynamic (free energy of adsorption) parameters obtained.     

Studies of protection of iron corrosion by rosin imidazoline self‐assembled monolayers

A type of rosin imidazoline (IM) has been synthesized using rosin acid and diethylenetriamine (DETA) as raw materials. The monolayers of IM were assembled on the surface of iron. The monolayers of the IM inhibitor were characterized by electrochemical impedance spectroscopy (EIS), electrochemical polarization curves and double‐layer capacitance. Surface analysis was carried out to establish the mechanism of corrosion inhibition of iron by X‐ray photoelectron spectroscopy (XPS) and scanning electron microscopy. The IM inhibitor showed good inhibition efficiency for iron in 0.1 M H₂SO₄. The inhibition mechanism of IM inhibitor was interpreted using molecular simulation. Copyright © 2006 John Wiley & Sons, Ltd.     

Green synthesis,electrochemical, and DFT studies on the corrosion inhibition of steel by some novel triazole Schiff base derivatives in hydrochloric acid solution

In this work, three triazole Schiff base derivatives 1-((1H-1,2,4-triazol-3-ylimino)methyl)naphthalen-2-ol (TMN), N-(furan-2-ylmethylene)-1H-1,2,4-triazol-3-amine (FTA) and N-(thiophen-2-ylmethylene)-1H-1,2,4-triazol-3-amine (TTA) were synthesized under ultrasonic irradiation and were investigated as corrosion inhibitors. FT-IR, NMR, and elemental analysis were used to elucidate the chemical structure of the synthesized inhibitors. The inhibitive characteristics of these inhibitors on C-steel corrosion in 1.0 M HCl were studied using three different techniques. The applied techniques were Electrochemical frequency modulation, electrochemical impedance spectroscopy, and potentiodynamic polarization curves. The acquired data from the experimental methods showed that the optimal concentration for TMN, FTA, and TTA is 1.0 × 10^?3 mol/L, and the inhibition efficiency reached up to 91.68%, 88.44%, and 87.29% for TMN, TTA, and FTA, respectively. Experiments also indicated that these compounds act as mixed-type inhibitors, and their concentration affects the inhibition efficiency in a directly proportional manner. Quantum paraments obtained from density functional theory (DFT) showed good agreement between experimental and computational results.     

Experimental and DFT analysis of onion peels for its inhibition behavior against mild steel corrosion in chloride solutions

Natural materials are good options for being used as inhibitors due to their high biodegradability, reasonable cost, easiness in use and high efficiency. In this regard, waste natural materials are very useful because they have all the properties of natural materials and easily available at very low cost (almost free). This work reports a similar kind of waste natural materials namely onion peels. The water extract of onion peels (WEOP) is characterized by UV–vis spectroscopy (UVS) and FTIR spectroscopy (FTIS). WEOP is tested for corrosion inhibition of mild steel (MS) in 1 M NaCl by various techniques like typical weight loss measurements (WLM), open circuit potential (OCP) curves, Tafel polarization (TP) curves, electrochemical impedance spectroscopy (EIS) and surface scanning microscopy (SEM). The maximum inhibition of mild steel corrosion is 90% (WLM). The reason of inhibition based on experimental analysis is proposed as adsorption of extract molecules on MS, which is found true in SEM images and Langmuir isotherm study. The WEOP is also examined by density functional theory principles, which recommends that the extract molecules can be easily adsorbed on MS and can stop corrosion of MS in NaCl solutions. Based on investigation, a schematic is introduced for compact explanation.     

Corrosion inhibition of 302 stainless steel with schiff base compounds

The effects of 2,2′-[bis-N(4-cholorobenzaldimin)]-1,1′-dithio (BCBD) and bis-(2-aminophenyl) disulphide (BAPD) on the corrosion behavior of 302 stainless steel in 0.5 M sulfuric acid solution as corrosive medium were investigated using weight loss and potentiostatic polarization techniques. Some corrosion parameters such as anodic and cathodic Tafel slopes, corrosion potential, corrosion current density, surface coverage degrees and inhibition efficiencies were calculated. The polarization measurements indicated that the inhibitors were of mixed type which inhibited corrosion by parallel adsorption on the surface of stainless steel due to the presence of more than one active centre in the inhibitor molecule. The adsorption followed Langmuir adsorption isotherm. The activation energy and thermodynamic parameters were calculated at different temperatures. Results showed that BCBD had a higher inhibition efficiency compared with BAPD.     

Electrochemical and Theoretical Studies of 1-Alkyl-2-substituted Benzimidazoles as Corrosion Inhibitors for Carbon Steel Surface in HCl Medium

The inhibition efficiencies of newly synthesized four 1-alkyl-2-substituted benzimidazole compounds(a~d) have been studied for the corrosion of carbon steel in 1.0 M HCl by using potentiodynamic polarization measurement. The four inhibitors act as mixed-type inhibitors,which mainly inhibit cathodes. The inhibition efficiency of these compounds enhanced when the concentration of the inhibitors increased. A theoretical study of the corrosion inhibition efficiency of these compounds was carried out by using the B3 LYP level with the 6-31+G* basis set. Considering the solvent effect,the IEFPCM model was selected. Furthermore,the adsorption energies of the inhibitors with the iron(001) surface were studied by using molecular dynamic(MD) simulations. The theoretical results show that these inhibitors all exhibit several adsorption active-centers. Meanwhile,the MD simulations indicate that the adsorption occurs mostly through benzene ring and the lone pair electrons of the nitro atoms. These results demonstrated that the theoretical studies and MD simulations are reliable and promising methods for analyzing the inhibition efficiency of organic inhibitors.     

Quantum chemical studies on some thiadiazolines as corrosion inhibitors for mild steel in acidic medium

Density functional theory at the B3LYP/6-31G(d,p) basis set level was performed on three thiadiazolines, namely 4-chloro-N-(5-phenyl-1,3,4-thiadiazol-2(3H)-ylidene)aniline (TD01), 4-chloro-N-(5-(4-methoxyphenyl)-1,3,4-thiadiazol-2(3H)-ylidene)aniline (TD02), and 2-(5-(4-chlorophenylimino)-4,5-dihydro-1,3,4-thiadiazol-2-yl) phenol (TD03), and the inhibitive effect of these thiadiazolines against the corrosion of mild steel in acidic medium is elucidated. The calculated quantum chemical parameters correlated to the inhibition efficiency are E_HOMO (highest occupied molecular orbital energy), E_LUMO (lowest unoccupied molecular orbital energy), the energy gap (ΔE) hardness (η), softness (S), dipole moment (μ), electron affinity (EA) ionization potential (IE), the absolute electro negativity (χ), and the fraction of electron transferred (ΔN). The decreasing order of %IE of the thiadiazolines studied was found to be in agreement with experimental corrosion inhibition efficiencies. The local reactivity has been analyzed through the condensed Fukui function and local softness indices using population analysis.     

Spectroscopy and rectification of three donor-sigma-acceptor compounds, consisting of a one-electron donor (pyrene or ferrocene), a one-electron acceptor (perylenebisimide), and a C19 swallowtail

We report spectroscopic characterization and unimolecular rectification (asymmetric electrical conduction) measurements of three donor-sigma-acceptor (D-sigma-A) compounds N-(10-nonadecyl)-N-(1-pyrenylmethyl)perylene-3,4,9,10-bis(dicarboximide) (1), N-(10-nonadecyl)-N-(4-[1-pyrenyl]butyl)perylene-3,4,9,10-bis(dicarboximide) (2), and N-(10-nonadecyl)-N-(2-ferrocenylethyl)perylene-3,4,9,10-bis(dicarboximide) (3). These molecules were arranged as one-molecule thick Langmuir-Blodgett monolayers between Au electrodes. In such an "Au | D-sigma-A | Au" sandwich, molecule 1 is a unimolecular rectifier, with rather small rectification ratios (between 2 and 3 at +/-1 V) that decrease upon cycling. Molecule 2 does not rectify. Molecule 3 rectifies, with a rectification ratio of between 14 and 28 at +/-1 V; the through-film rectification and currents persist, even with scans of +/-2 V, for up to 40 cycles of measurement. Qualitative arguments, based on a two-level rectification mechanism, are consistent with the current asymmetries observed in the monolayers of 1 and 3.     

Comparative study on the inhibitive effect of Sulfadoxine–Pyrimethamine and an industrial inhibitor on the corrosion of pipeline steel in petroleum pipeline water

The corrosion inhibition characteristics of Sulfadoxine plus Pyrimethamine (S&P) was evaluated and compared with the inhibition performance of an industrial corrosion inhibitor (S-Ind) under anaerobic condition. Modified gravimetric and electrochemical techniques were used. The corrosion inhibition efficiencies of both S&P and S-Ind were comparable for all the techniques applied. S&P gave slightly higher inhibition efficiency, while S-Ind gave a more steady corrosion protection. The corrosion inhibition efficiencies increased with increased concentration of both substances. The polarization curves showed mixed inhibition behavior for both S&P and S-Ind. A mechanism of chemisorption was proposed for the adsorption of S&P and S-Ind on pipeline steel surface, while the negative Gibbs free energy of adsorption values indicates a spontaneous adsorption process. The adsorption characteristics of the inhibitors were fitted into Langmuir adsorption isotherm.     

An experimental and theoretical investigation on adsorption properties of some diphenolic Schiff bases as corrosion inhibitors at acidic solution/mild steel interface

The effect of novel synthesized three Schiff bases, namely, 1,3-bis[2-(2-hydroxy benzylidenamino) phenoxy] propane (P1), 1,3-bis[2-(5-chloro-2-hydroxybenzylidenamino) phenoxy] propane (P2), and 1,3-bis[2-(5-bromo-2-hydroxybenzylidenamino) phenoxy] propane (P3), on the corrosion of mild steel in 0.1 M HCl was investigated using potentiodynamic polarization and electrochemical impedance spectroscopy methods. Polarization measurements suggest that P1 acts as mixed type inhibitor while P2 and P3 behave as mainly cathodic inhibitors for acidic corrosion of steel. All electrochemical measurements show that inhibition efficiencies increase with increase in inhibitor concentration. This reveals that inhibitive actions of inhibitors were mainly due to adsorption on steel surface. Adsorption of these inhibitors follows Temkin adsorption isotherm. The correlation between the adsorption ability of inhibitors and their molecular structures has been investigated using quantum chemical parameters obtained by MNDO semi-empirical method. Calculated quantum chemical parameters indicate that Schiff bases adsorbed on steel surface by chemical mechanism.     

硫酸溶液中1,1’-硫代羰基二咪唑在碳钢上的吸附及缓蚀影响和碘离子的增强效应

The inhibition effect of 1,1’-thiocarbonyldiimidazole (TCDI) on the corrosion behaviors of mild steel (MS) in 0.5 mol·L -1 H2SO4 solution was studied with the help of potentiodynamic polarization, electrochemical impedance spectroscopy (EIS), and linear polarization resistance (LPR) techniques. The effect of immersion time on the inhibition effect of TCDI was also investigated over 72 h. For the long-term tests, hydrogen evolution with immersion time (VH2-t) was measured in addition to the three techniques already mentioned. The thermodynamic parameters, such as adsorption equilibrium constant (Kads) and adsorption free energy (⊿Gads) values, were calculated and discussed. To clarify inhibition mechanism, the synergistic effect of iodide ion was also investigated. The potential of zero charge (PZC) of the MS was studied by electrochemical impedance spectroscopy method, and a mechanism of adsorption process was proposed. It was demonstrated that inhibition efficiency increased with the increase in TCDI concentration and synergistically increased in the presence of KI. The inhibition efficiency was discussed in terms of adsorption of inhibitor molecules on the metal surface and protective filmformation.     

新型咪唑啉化合物在H_2S/CO_2共存条件下对Q235钢的缓蚀性能

合成了一种新型咪唑啉化合物1-(2-氨基-硫脲乙基)-2-十五烷基-咪唑啉(IM-S),并通过失重法、电化学方法及扫描电镜等研究了IM-S在H2S/CO2共存条件下对Q235钢的缓蚀性能,探讨了其在Q235钢表面的吸附行为.结果显示,IM-S具有较好的抗H2S、CO2腐蚀能力,能同时抑制碳钢腐蚀的阴、阳极反应过程,最高缓蚀效率可达92.74%.缓蚀剂在Q235钢表面呈单分子层吸附,属于以化学吸附为主的混合吸附.最后采用量子化学方法对IM-S的缓蚀机理做了进一步分析.     

阳离子型可聚合咪唑类离子液体-丙烯酰胺共聚物的制备及其对盐酸腐蚀碳钢缓蚀行为

利用阳离子型可聚合离子液体1-丙烯酰氧乙基-3-甲基咪唑四氟硼酸盐与丙烯酰胺的反相微乳液共聚合,制备了阳离子型咪唑类离子液体-丙烯酰胺共聚物缓蚀剂,并探讨了其缓蚀性能。研究了不同阳离子度、不同浓度聚合物溶液的缓蚀性能以及吸附时间对盐酸腐蚀碳钢速率的影响,并初步讨论了缓蚀机理。研究表明,该种阳离子型缓蚀剂的缓蚀效率可达90%以上;缓蚀剂的缓蚀能力不仅取决于缓蚀剂的阳离子度,还取决于该种缓蚀剂的相对分子质量;缓蚀效率并非简单地随聚合物浓度的增加而提高,当聚合物溶液的浓度过高时,反而会使缓蚀效率下降;随吸附时间的延长,碳钢的腐蚀速率逐渐降低,约40 h后基本保持不变;加入缓蚀剂有效抑制了酸对铁的腐蚀,随缓蚀效率的提高,碳钢表面的粗糙程度明显降低,孔洞结构减少。