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Date palm leaves (DPL) was extracted using acetone (ACE), ethanol (ETH), aqueous (AE), butanol (BUT), methanol (METH), isopropanol (ISO), and ethyl acetate (EHY ACT). The extracts were characterized using Fourier-transform infrared spectroscopy (FTIR) and ultraviolet-visible (UV-vis) spectroscopy. The various solvent DPL extracts were screened for anticorrosion property against low carbon steel in 15 wt.% HCl solution at 25 °C. ACE, AE, and ETH DPL extracts are found to promote the corrosion of the low carbon steel while BUT, ISO, METH, and EHY ACT DPL extracts exhibit anticorrosion property. However, BUT DPL extract shows the best anticorrosion property with 400 ppm protecting the low carbon steel by 82%. Based on the results from the screening experiments, BUT extract was selected for a comprehensive corrosion inhibition study. Inhibition effectiveness of BUT DPL extract is found to increase with increasing concentration with 1000 ppm affording 97% protection at 25 °C. The inhibition performance increases up to 40 °C but slightly decreases as the temperature was raised to 50 °C and 60 °C. However, BUT DPL extract could afford 86% protection at 60 °C. Scanning electron microscope and atomic force spectroscopy results confirm that BUT DPL extract is indeed an effective inhibitor for X60 carbon steel in 15 wt.% HCl solution.
Asunto(s)
Phoeniceae , Acero , Carbono , Corrosión , Extractos Vegetales , Hojas de la Planta , SolventesRESUMEN
Chitosan/silver nanofluids were prepared using Phoenix dactylifera (DPLE) or Rumex vesicarius (HEL) extracts as the reducing agent, characterized using Fourier-transform infrared spectroscopy (FTIR), ultraviolet-visible (UV-vis), X-ray diffraction (XRD), and transmission electron microscope (TEM). The antimicrobial effect of the nanofluids against Gram positive, Bacillus licheniformis, Staphylococcus haemolyticus, Bacillus cereus, and Micrococcus luteus, and Gram-negative Pseudomonas aeruginosa, Pseudomonas citronellolis, and Escherichia coli bacteria has been studied. The nanoparticles were polydispersed in the chitosan matrix and are highly stable. The zeta potential of the silver nanoparticles in DPLE- and HEL-mediated composites is +46 mV and +56 mV, respectively. The FTIR results reveal that the free carboxylate groups in the plant biomaterial took part in stabilization process. HEL is a stronger reducing agent than DPLE and nanoparticles generated with HEL are smaller (8.0-36 nm) than those produced with DPLE (10-43 nm). DPLE- and HEL-mediated composites effectively inhibit the growth of the studied bacteria but HEL-mediated composite exhibited higher effect. The higher antimicrobial activity of HEL-mediated composite is linked to the smaller nanoparticles. The foregoing results indicate that HEL extract can be used in the green production of potential antimicrobial chitosan/silver nanofluids for biomedical and packaging applications.
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Seven natural polymers namely, chitosan (CHI), dextran (Dex), carboxymethyl cellulose (CMC), sodium alginate (ALG), pectin (PEC), hydroxylethyl cellulose (HEC), and Gum Arabic (GA) were screened for anticorrosion property towards AZ31â¯Mg alloy in 3.5â¯wt.% NaCl solution. CHI, Dex, CMC, PEC, and GA accelerated the corrosion while ALG and HEC moderately inhibited the corrosion of the alloy. HEC and ALG (1â¯g/L) protected the alloy by 64.13 % and 58.27 %, respectively. Two inhibitor cocktails consisting of either HEC or ALG, KI, and Date palm seed oil have been formulated. HEC- and ALG-formulations inhibited the alloy corrosion by 80.56 % and 77.43 %, respectively from EIS technique. Surface observation studies using SECM, AFM, SEM, and EDX agreed with other experimental results revealing effective corrosion inhibition by the formulations. X-ray photoelectron spectroscopy, FTIR, and UV-vis results disclose that Mg(OH)2 co-existed with adsorbed inhibitor complexes.
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Aleaciones/química , Materiales Biocompatibles Revestidos/química , Corrosión , Polímeros/química , Adsorción/efectos de los fármacos , Alginatos/química , Carboximetilcelulosa de Sodio/química , Quitosano/química , Goma Arábiga/química , Magnesio/química , Ensayo de Materiales , Propiedades de SuperficieRESUMEN
The possibility of utilizing dextran as a green corrosion inhibitor for steel in strong acid environment was explore using weight loss, electrochemical (electrochemical impedance spectroscopy (EIS), electrochemical frequency modulation (EFM), potentiodynamic polarization (PDP), and linear polarization (LPR)) supported with surface analysis via scanning electron microscopy (SEM), energy dispersive X-ray spectroscopy (EDAX), atomic force microscopy (AFM), and X-ray photoelectron spectroscopy (XPS) techniques. The effect of molecular weight, temperature, and modification on the inhibition efficiency of dextran was also studied. Results from all the applied techniques reveal that dextran exhibit moderate anticorrosion property toward St37-2 steel dissolution in 15% H2SO4 solution. Dextran with molecular weight of 100â¯000-200â¯000 g/mol (Dex 1) exhibited the highest inhibition efficiency of 51.38% at 25 °C. Based on PDP results, dextran behaved as a mixed type corrosion inhibitor. Inhibition efficiency of dextran varies inversely with molecular weight but directly with temperature. Two modification approaches, namely incorporation of silver nanoparticles (AgNPs) into dextran matrices and combination with 1 mM KI were adopted to enhance the inhibition efficiency of dextran and the approaches proved effective. The protective capability of Dex 1 has been upgraded from 51.38% to 86.82% by infusion of AgNPs and to 94.21% by combination with KI at 25 °C. Results from the study on the effect of temperature reveals that Dex 1 + KI mixture could synergistically offer 99.4% protection to St37-2 steel in 15% H2SO4 environment at 60 °C. Surface analysis results confirm the presence of additives molecules on the studied metal surface. XPS results disclose that AgNPs are in oxide form while iodide ions are in the form of triiodide and pentaiodide ions on the metal surface. Modified dextran is a promising candidate for application as corrosion inhibitor in acid induced corrosive environment.
RESUMEN
Two isoxazolidine derivatives namely 5-(benzo[d][1,3]dioxol-5-ylmethyl)-2-tetradecyl isoxazolidine (BDMTI) and 5-(4-hydroxy-3-methoxybenzyl)-2-tetradecyl isoxazolidine (HMBTI) were synthesized and characterized using FTIR, C-NMR, H-NMR, and elemental analysis. The synthesized compounds were evaluated as corrosion inhibitors for API 5L X60 steel in 1 M HCl in the temperature range of 25-60 °C using gravimetric and electrochemical (Electrochemical Impedance Spectroscopy (EIS), Potentiodynamic Polarization (PDP) and Linear Polarization Resistance (LPR)) techniques. The effect of addition of a small amount of iodide ions on the corrosion inhibition performance of the compounds was also assessed. In addition, quantum chemical calculations and Monte Carlo simulations were employed to correlate the electronic properties of the compounds with the corrosion inhibition effect as well as to evaluate the adsorption/binding of the inhibitor molecules on the steel surface. Experimental results show that the two compounds inhibited the corrosion of carbon steel in an acid environment with HMBTI showing superior performance. The corrosion inhibition effect was found to be dependent on the inhibitors' concentration and temperature. Addition of iodide ions improves the inhibition efficiency considerably due to co-adsorption of the iodide ions and the inhibitors on the steel surface which was competitive in nature as confirmed from the synergistic parameter (S 1) which was less than unity at higher temperature. Experimental and theoretical results are in good agreement.
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Gemini surfactant, N,N'-dialkylcystine 2(C12Cys), derived from cystine, and a monomeric N-alkyl cysteine counterpart, (C12Cys), were synthesized and purified. The characterization of surfactants 2(C12Cys) and (C12Cys) was made by Fourier transform infrared, 1H NMR, and elemental analysis. The effect of 2(C12Cys) and (C12Cys) on mild steel (MS) corrosion in 1 M HCl solution was explored as a function of their concentration and electrolyte temperature by means of gravimetric and electrochemical experiments (potentiodynamic polarization and Electrochemical impedance spectroscopy), surface analytical techniques (scanning electron microscopy (SEM)/energy dispersive X-ray spectroscopy (EDAX) and atomic force microscopy (AFM)) and theoretical study. The investigated compounds exhibited surface active properties and performed as good inhibitors for corrosion control of mild steel (MS) in acid solution. However, compared to monomeric (C12Cys), Gemini surfactant 2(C12Cys) showed high corrosion inhibiting ability at very low concentration. The EIS results revealed a greater charge transfer resistance in 2(C12Cys) solution compared to that in (C12Cys) solution. SEM/EDAX observations validate the development of an inhibitive film by the adsorbed molecules of surfactant on the MS surface. The AFM micrographs supported the SEM/EDAX results and exhibited a lowering in the roughness of the corroded MS surface in the presence of both (C12Cys) and 2(C12Cys) surfactants. Further, quantum chemical calculations and Monte Carlo simulations were used to study the dependence of corrosion inhibiting efficacy on the molecular structure and adsorption strength.
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Polyurethane based tri-block copolymers namely poly(N-vinylpyrrolidone)-b-polyurethane-b-poly(N-vinylpyrrolidone) (PNVP-PU) and poly(dimethylaminoethylmethacrylate)-b-polyurethane-b-poly(dimethylaminoethylmethacrylate) (PDMAEMA-PU) were synthesized through atom transfer radical polymerization (ATRP) mechanism. The synthesized polymers were characterized using nuclear magnetic resonance (NMR) spectroscopy and gel permeation chromatography (GPC) methods. The corrosion inhibition performances of the compounds were investigated on mild steel (MS) in 0.5 M H2SO4 medium using electrochemical measurements, surface analysis, quantum chemical calculations and molecular dynamic simulations (MDS). Potentiodynamic polarization (PDP) measurements revealed that the polymers are mixed-type corrosion inhibitors. Electrochemical impedance spectroscopy (EIS) measurements showed that the polymers inhibit MS corrosion by adsorbing on MS surface to form pseudo-capacitive interface. The inhibitive effects of the polymers increase with increasing concentration and decrease with increasing temperature. The adsorption of both the polymers on MS surface obey the Langmuir adsorption isotherm and involves both physisorption and chemisorption mechanisms. Scanning electron microscopy (SEM) and atomic force microscopy (AFM) analyses showed that the polymers formed protective film on MS surface and shield it from direct acid attack. Quantum chemical calculations and molecular dynamic simulations studies corroborate experimental results.
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The inhibition of the corrosion of N80 steel in 3.5 wt. % NaCl solution saturated with CO2 by four porphyrins, namely 5,10,15,20-tetrakis(4-hydroxyphenyl)-21H,23H-porphyrin (HPTB), 5,10,15,20-tetra(4-pyridyl)-21H,23H-porphyrin (T4PP), 4,4',4â³,4â´-(porphyrin-5,10,15,20-tetrayl)tetrakis(benzoic acid) (THP) and 5,10,15,20-tetraphenyl-21H,23H-porphyrin (TPP) was studied using electrochemical impedance spectroscopy (EIS), potentiodynamic polarization, scanning electrochemical microscopy (SECM) and scanning electron microscopy (SEM) techniques. The results showed that the inhibition efficiency, η% increases with increasing concentration of the inhibitors. The EIS results revealed that the N80 steel surface with adsorbed porphyrins exhibited non-ideal capacitive behaviour with reduced charge transfer activity. Potentiodynamic polarization measurements indicated that the studied porphyrins acted as mixed type inhibitors. The SECM results confirmed the adsorption of the porphyrins on N80 steel thereby forming a relatively insulated surface. The SEM also confirmed the formation of protective films of the porphyrins on N80 steel surface thereby protecting the surface from direct acid attack. Quantum chemical calculations, quantitative structure activity relationship (QSAR) were also carried out on the studied porphyrins and the results showed that the corrosion inhibition performances of the porphyrins could be related to their EHOMO, ELUMO, ω, and µ values. Monte Carlo simulation studies showed that THP has the highest adsorption energy, while T4PP has the least adsorption energy in agreement with the values of σ from quantum chemical calculations.
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Simulación por Computador , Electroquímica , Método de Montecarlo , Porfirinas/química , Relación Estructura-Actividad Cuantitativa , Teoría Cuántica , Cloruro de Sodio/química , Acero/química , Adsorción , Corrosión , Espectroscopía Dieléctrica , Electrones , Microscopía Electrónica de Rastreo , Soluciones , TermodinámicaRESUMEN
The corrosion inhibition effect of pectin (a biopolymer) for X60 pipeline steel in HCl medium was investigated using weight loss, electrochemical, water contact angle measurements, and scanning electron microscopy techniques. The results obtained show that pectin acts as a good corrosion inhibitor for X60 steel. Inhibition efficiency increased with increase in pectin concentration and temperature. Potentiodynamic polarization results reveal that pectin could be classified as a mixed-type corrosion inhibitor with predominant control of the cathodic reaction. The effective corrosion inhibition potential of pectin could be related to the adsorption of pectin molecules at the metal/solution interface which is found to accord with the Langmuir adsorption isotherm model and a protective film formation. Quantum chemical calculations provided insights into the active sites and reactivity parameters governing pectin activity as a good corrosion inhibitor for X60 steel.