Expired pharmaceutical compounds as potential inhibitors for cast iron corrosion in acidic medium

The inhibition potential of some expired waste pharmaceutical drugs, namely cefpodoxime (CF), levofloxacin (LV), ofloxacin (OX) and linezolid (LZ) on cast iron corrosion in 1 M HCl has been tested for the first time by chemical (weight loss) and electrochemical (Tafel polarization and impedance spectroscopy) methods. At a constant acid concentration (1 M HCl), the inhibition efficiency (IE%) increased with the increase of the inhibitors’ concentration. At optimum inhibitor concentration, the CF exhibited the highest inhibition efficiency (95.2%). Inhibitors were adsorbed on the cast iron surface through the Langmuir adsorption isotherm at all concentrations and temperatures studied. Antagonism and synergism arising between the halide ions and the inhibitors were also explained. Thermodynamic parameters have been calculated and are discussed. Tafel polarization curves pointed to all inhibitors acting as mixed-type. Corrosion inhibition properties of the inhibitors have been inferred from FT-IR spectra, UV–Vis spectra, surface morphological analysis and wide-angle X-ray diffraction studies.     

Electrochemical investigation of a schiff base synthesized by cinnamaldehyde as corrosion inhibitor on mild steel in acidic medium

The inhibiting effect of (NE)-4-phenoxy-N-(3-phenylallylidene) aniline (PAC) on the corrosion of mild steel in 1.0 M HCl has been studied by electrochemical impedance spectroscopy, and Tafel polarization measurements. The corrosion rate was also calculated theoretically in terms of mm per year and mil per year, using current density values of mild steel in 1.0 M HCl medium. It was found that PAC has a remarkable inhibition efficiency on the corrosion of mild steel especially at high temperatures. The values of E _a obtained in presence of a Schiff base were found to be lower than those obtained in the inhibitor-free solution. The increase of inhibition efficiency percent with temperature increase was associated with the transformation of physical adsorption into chemical adsorption. The thermodynamic functions of adsorption processes have been evaluated and discussed at each temperature. Scanning electron microscope observations of the electrode surface confirmed the existence of a protective adsorbed film of the inhibitor on the electrode surface.     

Inhibitive effect by extract of Mentha rotundifolia leaves on the corrosion of steel in 1 M HCl solution

An extract of Mentha rotundifolia leaves (EMRL) was tested as a corrosion inhibitor of steel in 1 M HCl using electrochemical impedance spectroscopy, Tafel polarization methods, and weight loss measurements. The inhibition efficiency of the extract of Mentha rotundifolia leaves was calculated and compared. We note good agreement between these methods. The results obtained revealed that the inhibitor tested differently reduced the kinetics of the corrosion process of steel. Its efficiency increases with the concentration and attained 92.87 % at 35 %. The effect of temperature on the corrosion behavior of steel in 1 M HCl was also studied in the range 298 and 338 K. The thermodynamic data of activation were determined. Mentha rotundifolia extract is adsorbed on the steel surface according to a Langmuir adsorption model.     

Influence of acid treatment on structure of clinoptilolite tuff and its adsorption of methane

This study presents the results of the methane adsorption properties of clinoptilolite tuff from Bigadic, Turkey and that of acid treated forms at 273 and 293 K up to 100 kPa using volumetric apparatus. In order to assess changes in structural and gas adsorption properties of clinoptilolite, zeolite sample was treated with acid solutions of varying concentrations (0.1, 0.5, 1.0 and 2.0 M) at 70 °C during 3 h. Structural and thermal characterization of natural and acid treated clinoptilolite samples were carried out using a combination of techniques such as X-ray diffraction, X-ray fluorescence, thermogravimetric, differential thermal analysis and nitrogen adsorption methods. At both temperatures, uptake of methane (CH₄) increased in the following order: CLN < CLN-H2 < CLN-H1 < CLN-H05 < CLN-H01. CH₄ adsorption capacities of the original and acid treated clinoptilolites were found in the range of 0.476–0.910 mmol/g and 0.398–0.691 mmol/g at 273 and 293 K, respectively.     

Monitoring corrosion and corrosion control of low alloy ASTM A213 grade T22 boiler steel in HCl solutions

Rates of corrosion of low alloy ASTM A213 grade T22 boiler steel were monitored in aerated stagnant 0.50 M HCl solutions at different temperatures (283–303 K) using Tafel extrapolation method and the non-destructive electrochemical frequency modulation (EFM) technique, complemented with XPS examinations. Serine (Ser) was introduced as a corrosion-safe inhibitor. Corrosion rates (in μm y^?1) obtained from these two methods was in good agreement. Tafel plots showed that Ser acted mainly as a cathodic-type inhibitor. The inhibition process was attributed to the formation of an adsorbed film on the metal surface that protects the metal against corrosive agents. XPS examinations of the electrode surface confirmed the existence of such adsorbed film. The inhibition efficiency increased with increase in Ser concentration, while it decreased with temperature, suggesting physical adsorption. Activation energies have been calculated in the absence and presence of various concentrations of Ser by measuring the temperature dependence of the corrosion rate obtained from the two methods employed. It was found that the activation energy in the presence of Ser is higher than that in bare HCl solution. The adsorptive behaviour of Ser followed Temkin-type isotherm. The standard free energy of adsorption was estimated to be ?25 kJ mol^?1 at 303 K. These results confirmed the occurrence of physical adsorption.     

Experimental study of inhibition of corrosion of mild steel in 1 M HCl solution by two newly synthesized calixarene derivatives

Inhibition of the corrosion of mild steel in molar hydrochloric acid by two calixarenes, including the effect of inhibitor concentration and temperature, has been investigated by use of weight loss and electrochemical measurements (polarisation and impedance). The results obtained showed that the rate of corrosion decreased substantially in the presence of the compounds, with maximum inhibition of 98.2 % by one of the compounds at a concentration of 10^?3 M. The effect of temperature on corrosion behaviour in the presence of different concentrations of the two new calixarenes was studied in the range 45–75 °C. The efficiency of inhibition by the compounds increased with increasing inhibitor concentration and was independent of temperature. Polarisation curves revealed that the calixarenes are mixed-type inhibitors. Adsorption of the inhibitors by the carbon steel surface obeyed the Langmuir adsorption isotherm. Some thermodynamic data for the dissolution and adsorption processes were also determined.     

Corrosion protection of carbon steel in acidic media by expired bupropion drug; experimental and theoretical study

The effects of expired bupropion on the corrosion protection of carbon steel in hydrochloric acid (1.0 M) and sulfuric acid (0.5 M) solutions were examined by Fourier transform infrared (FTIR) spectroscopy, Tafel polarization and electrochemical impedance spectroscopy (EIS). Bupropion concentrations in both acid solutions were raised, which improved corrosion prevention. Bupropion was a mixed inhibitor because it retarded the anodic and cathodic processes, as indicated by polarization data. The inhibition efficiency decreased with the increasing temperature from 25 to 55 °C. In the presence of bupropion, the activation energies of corrosion in both acid solutions increased. The thermodynamic quantities were deduced from the influence of temperature on the corrosion process of carbon steel in both acid media. Bupropion adsorption on carbon steel followed the Langmuir adsorption isotherm. The polarization data yielded outcomes consistent with the results arising from impedance measurements. FTIR spectroscopy showed the active sites of bupropion molecule during adsorption on the alloy surface. The theoretical study and molecular dynamics simulation of bupropion was done by a density functional theory (DFT) approach to realize the effects of molecular structure on the inhibitive action of bupropion.     

MPEC-IMI as an effective green inhibitor to protect Q235 steel in 0.5 M HCl medium

Imidazole (IMI)-based polyethylene glycol monomethyl ether (MPEC-IMI) as a novel green corrosion inhibitor was synthesized to protect the Q235 steel in 0.5 M HCl corrosive medium at 318 K. The inhibition performance of MPEC-IMI was investigated by weight loss measurement, the electrochemical method (Tafel and EIS) and surface analysis (SEM and EDX). The results reveal that the MPEC-IMI shows enhanced anticorrosion performance for carbon steel, which is attributed to the formation of the adsorptive protection film on the surface, and the type of adsorption basically obeys the Langmuir monolayer adsorption. Furthermore, when the concentration of MPEC-IMI is 300 mg L^?1, the corrosion inhibition efficiency can reach up to 92.00%. In support of further study of the corrosion inhibition behavior by virtue of quantum chemical calculation and molecular dynamics simulations, the results show that the MPEC-IMI molecule has high reactivity and strong interaction on the iron surface.     

Etude du pouvoir inhibiteur de la 2,9-chlorométhyl-1,10-phénanthroline pour la corrosion d'un acier doux en milieu HCL 1M A 90 °C

The corrosion behaviour of mild steel in 1M HCl containing organic compounds such as: 2,2′-bipyridine (inh1), 1,10-phenanthroline (inh2), 4,4′-6,6′-tetramethyl-2,2′-bipyridine (inh3) and 2,9-chloromethyl-1,10-phenanthroline (inh4), was studied by weight loss and electrochemical polarization methods. Polarization data indicate that all tested compounds are mixed-type inhibitors affecting both cathodic and anodic processes. The inhibition efficiency of these additives increases in the order: inh3 < inh1 < inh2 < inh4. The adsorption of 2,9-chloromethyl-1,10-phenanthroline on the mild steel surface in 1M HCl medium follows a Langmuir adsorption isotherm. The effect of temperature indicates that the inhibition efficiency of inh4 is temperature independent in the range 25 to 90 °C. The apparent activation energies in the absence and in the presence of inh4 were determined.     

Quaternary Ammonium Salts from Hydrolyzed Fatty Oil Based on Novel Tertiary Amines Used as Corrosion Inhibitors for Pipelines Carbon Steel at Acid Job in Petroleum Industry

Ten new quaternary ammonium salts (QASs) were designed and synthesized from hydrolyzed fatty oils; the hydrolyzed oils were used as a source of alkyl halides to prepare the QASs by refluxing the fatty alkyl halide with ethoxylated amines as untraditional 3° amines in acetone. The structure of the prepared QASs were characterized by FTIR and ¹H NMR spectroscopy. The prepared cationic surfactants QASs were tested as corrosion inhibitors for carbon steel in 1 M HCl solution. The corrosion inhibition efficiency was measured using weight loss and potentiodynamic polarization methods. The inhibition efficiencies obtained from the two employed methods are in good agreement with each other. In generally, the inhibition efficiency increased with increasing the inhibitor concentration. From the obtained data it was found that the inhibition efficiency of QASs, which, based on ethoxylated aromatic tertiary amine, is greater than the efficiencies of the QASs based on ethoxylated aliphatic tertiary amine. The QASs based on fatty alkyl halide from palm oil exhibited the best inhibition efficiency than QASs based on fatty alkyl halides from coconut oil. The potentiodynamic polarization measurements indicated that the inhibitors are of mixed type. The adsorption of the inhibitors on the carbon steel surface in the acid solution was found to obey Langmuir's adsorption isotherm. The free energy of adsorption processes was calculated and discussed. The surface active properties were calculated on the basic of surface tension measurements. The obtained data of inhibition efficiencies were discussed on the light of surface active properties of these QASs and their chemical structures. The quantum chemical calculations was proceeded for QHL1,4,5 and QHP3,4,5 the following quantum chemical indices such as the bond length, bond angle, charge density distribution, highest occupied molecular orbital (HOMO), the lowest unoccupied molecular orbital (LUMO), energy gap ΔE?HOMO –LUMO, and dipole moment (u) were considered.The surface morphology of carbon steel sample was investigated by scanning electron microscopy.     

Adsorption,Surface Morphological,and Electrochemical Studies on the Inhibitive Properties of 4-(N,N-dimethylaminobenzilidine)-3-mercapto-6-methyl-1, 2, 4-triazin (4H)-5-one (DAMMT) on Mild Steel in 0.5 N H2SO4

Inhibition of mild steel corrosion in 0.5 N sulfuric acid by 4-(N, N-dimethylaminobenzilidine)-3-mercapto-6-methyl-1, 2, 4-triazin (4H)-5-one (DAMMT) was studied using polarization studies (Tafel); electrochemical impedance spectroscopy studies (EIS), adsorption studies, and surface morphological studies (SEM and AFM). The effect of inhibitor concentrations on corrosion rate, the effect of temperature, degree of surface coverage, adsorption kinetics, and surface morphology are investigated. Results show that the rate of corrosion increases with temperature in the absence and presence of inhibitor. Activation energies and enthalpies of activation in the presence and absence of DAMMT were obtained by measuring the temperature dependence of the corrosion current. DAMMT exhibits excellent inhibition properties towards MS and act as a mixed type inhibitor.     

Corrosion inhibition and adsorption behavior of imidazoline salt on N80 carbon steel in CO2-saturated solutions and its synergism with thiourea

The inhibition and adsorption behavior of 2-undecyl-1-sodium ethanoate-imidazoline salt (2M2) and thiourea (TU) on N80 mild steel in CO₂-saturated 3 wt.% NaCl solutions was studied at 25?°C, pH 4, and 1 bar CO₂ partial pressure using electrochemical methods. It was found that inhibition efficiency (η%) increased with increase in 2M2 concentration but decreased with increase in TU concentration with optimum η% value at 20 mg l^?1 TU. The data suggest that the compounds functioned via a mixed-inhibitor mechanism. The inhibition process is attributed to the formation of an adsorbed film of 2M2 and TU via the inhibitors polycentric adsorption sites on the metal surface which protects the metal against corrosion. A synergistic effect was observed between TU and 2M2. Potential of unpolarizability, E _u, was observed in the presence of 100 mg l^?1 TU which was shifted positively in the presence of 2M2–100 mg l^–1 TU blends, which suggests that the presence of 2M2 stabilized the adsorption of TU molecules on the surface of the metal. The adsorption characteristics of 2M2 were approximated by Langmuir adsorption isotherm.     

Inhibition of acid corrosion of carbon steel using aqueous extract of olive leaves

The inhibitive action of the aqueous extract of olive (Olea europaea L.) leaves toward the corrosion of C-steel in 2 M HCl solution was investigated using weight loss measurements, Tafel polarization, and cyclic voltammetry. It was found that the extract acts as a good corrosion inhibitor for the tested system. The inhibition efficiency increases with increasing extract concentration. The inhibitive action of the extract is discussed with a view to adsorption of its components onto the steel surface, making a barrier to mass and charge transfer. The adsorption of extract components onto the steel surface was found to be a spontaneous process and to follow the Langmuir adsorption isotherm. It was found also that such adsorption increases the activation energy of the corrosion process. The results of cyclic voltammetry showed that the presence of olive extract decreases the charge density in the transpassive region. The inhibition efficiency is greatly reduced as the temperature is increased.     

Phytochemical compounds and anti-corrosion activity of Veronica rosea

The aim of this work is the phytochemical study of the butanolic extract of the aerial parts of Veronica rosea. Four compounds 1–4 have been isolated using different chromatographic methods. The structures of these compounds were determined by NMR spectral analysis and mass spectroscopy. The adsorption and anticorrosion effects of this extract were investigated towards the corrosion of copper in 1 M HNO₃ aqueous by the weight loss technique and potentiodynamic polarization. The results showed that the butanolic extract is a good inhibitor and the inhibition efficiency increases with increasing of concentration of the inhibitor. The adsorption of this extract on the copper specimen surface was spontaneous and obeyed the Langmuir’s adsorption isotherm. Large value of adsorption equilibrium Constant (K _ads = 35 L g^?1) was obtained. The polarization experiments confirmed the data obtained by gravimetric weight-loss. Tafel plot of polarization curves indicates that the extract acts as a mixed type inhibitor.     

Nonionic Surfactants from Recycled Poly(ethylene terephthalate) as Corrosion Inhibitors of Steel in 1 M HCl

Recycled poly(ethylene terephthalate) (PET) can be modified to produce nonionic surfactants. Recycling of PET waste was carried out in presence of triethanolamine and manganese acetate as catalyst. The produced oligomers were reacted with stearic acid and polyethylene glycol, PEG, which have different molecular weights 400, 1,000, and 4,000. The inhibition of corrosion of steel in 1 molar hydrochloric acid solution in the presence of the prepared surfactants is studied by weight loss and electrochemical polarization measurements. The polarization curves indicate that these compounds act as mixed‐type inhibitors. The inhibition efficiency increases with the increase of inhibitor concentration to reach their critical micelle concentrations. The temperature effect on the corrosion behavior of steel in 1 M HCl with and without surfactants is studied in the temperature range from 308 to 343 K. The adsorption of inhibitors on the steel surface is found to increase with increasing the temperature. From the adsorption isotherm, some thermodynamic data for the adsorption process are calculated and discussed.     

Biosorption of strontium from aqueous solutions onto spent coffee grounds

A set of experiments was carried out to evaluate the strontium uptake potential of spent coffee grounds (SCG) by batch tests in aqueous medium. Adsorption of Sr²⁺ as a function of contact time and adsorbent dose, pH, particles size, agitation speed, temperature and co-ions presence was investigated. Obtained results revealed that the maximum adsorption took place at pH range of 5–8 and temperature values between 283 and 333 K. Particles size effect was not very significant and agitation speed influenced on the equilibrium time. Competitive adsorption experiments allowed us to classify the negative effect on the Sr²⁺ uptake according to this order Al³⁺ ? Co²⁺ > Mg²⁺ > Ca²⁺ ? Na⁺ > K⁺ > Cs⁺. Kinetic study indicated that the Sr²⁺ uptake was fast and it was well fitted by the pseudo second order reaction model. Adsorption isotherm was well interpreted by Langmuir model. The maximum adsorption capacity was found to be 69.01 mg g^?1 at pH 7, 293 K, particles sizes = 200–400 μm and agitation speed 250 rpm. The thermodynamic study revealed that the process was spontaneous (ΔG ⁰ < 0), exothermic (ΔH ⁰ < 0) with a raised affinity for Sr²⁺ (ΔG ⁰ < 0, ΔS ⁰ > 0) and occurred by physical adsorption (E _a = 8.37 kJ mol^?1). FTIR analysis showed carboxylic acid and amino group presence on SCG surface playing a vital role in Sr²⁺ biosorption.     

Electrochemical studies on the interaction of l-cysteine with metallic copper in sulfuric acid

Amino acids have been widely used as green corrosion inhibitors for an array of metals. Considering its importance in corrosion chemistry, studies were undertaken with the objective to discovering the inhibitory effect of a sulfur-containing amino acid, l-cysteine, on copper in different concentrations of sulfuric acid (0.5, 1.0, and 1.5 M) at different temperatures. Techniques like the weight loss method, electrochemical impedance spectroscopy, potentiodynamic polarization (Tafel), and adsorption studies were employed. Results revealed that l-cysteine do offer an attractive inhibition efficiency. However, with an increase in the concentration of the inhibitor, corrosion rates decreased irrespective of the temperature gradients. This is due to surface adsorption of the inhibitor molecules on the metal which has contributed to a decreased double-layer capacitance and increased polarization resistance. With the increase in the concentration of the medium, the corrosion rate was also enhanced and this is due the liberation of a high quantum of H⁺ ions. Based on the results of Tafel polarization studies, it is evident that the amino acid, l-cysteine, could act as a mixed type inhibitor. The importance of l-cysteine in the corrosion of copper metal has been highlighted in this paper.     

Surface morphological and impedance spectroscopic studies on the interaction of polyethylene glycol (PEG) and polyvinyl pyrrolidone (PVP) with mild steel in acid solutions

The inhibition of mild steel corrosion in aerated acid mixture of 0.5 N H₂SO₄ and 0.5 N HCl solution was investigated using potentiodynamic polarization studies, linear polarization studies, electrochemical impedance spectroscopy, adsorption, and surface morphological studies. The effect of inhibitor concentration on corrosion rate, degree of surface coverage, adsorption kinetics, and surface morphology is investigated. The inhibition efficiency increased markedly with increase in additive concentration. The presence of PEG and PVP decreases the double-layer capacitance and increases the charge-transfer resistance. The inhibitor molecules first adsorb on the metal surface following a Langmuir adsorption isotherm. Both PEG and PVP offer good inhibition properties for mild steel and act as mixed-type inhibitors. Surface analysis by scanning electron microscopy (SEM) and atomic force microscopy (AFM) shows that PVP offers better protection than PEG.     

Cloud Point Phenomenon in Amphiphilic Drug Promethazine Hydrochloride+Electrolyte Systems

Herein we report clouding phenomenon occurring in amphiphilic drug promethazine hydrochloride (PMT) in the presence of electrolytes. The CP of 50 mM drug solution, prepared in 10 mM sodium phosphate buffer, was found to decrease with increasing pH due to deprotonation of drug molecules at high pH. Addition of inorganic salts (KF, KCl and KBr) to drug solutions at fixed pH (6.7) and drug concentration (50 mM) caused an increase in CP. The results have been discussed on the desorption/adsorption of counterions to the headgroups. Cations also increased the CP by affecting the water structure with their effectiveness being in the order: Li⁺<Na⁺<K⁺<NH₄ ⁺. In the presence of NaCl, increase in drug concentration increased the CP while increase in pH showed an opposite trend.     

Effect of MW and pH on poly(ethylene glycol) adsorption onto carbon

Poly(ethylene glycol) (PEG) is a water-soluble polymer commonly found in industrial and domestic wastewaters. In this study the adsorption onto granular activated carbon (GAC) of PEG, of different molecular weights, from aqueous solutions was examined to evaluate its applicability to wastewater treatment. Batch kinetic models have been tested to predict the rate constant of adsorption. The amount of PEG adsorbed on activated carbon depends mainly on the pH, the MW and on the solution characteristics. The adsorption at fixed temperature decrease by MW (PEG-8000 < PEG-3350 < PEG-1450) a polymer chain conformation modification can explain these effect. The large values of adsorption capacity (>350 mg/g) at low and high pH values show a great potential for GAC. The adsorption process can be described well with the Langmuir and the pseudo first order equation. The effective intraparticle diffusion coefficients of PEG molecules in the GAC adsorbent varying according to the MW values in the range 8.45 × 10^?3–9.71 × 10^?7.