Chemically modified guar gum and ethyl acrylate composite as a new corrosion inhibitor for reduction in hydrogen evolution and tubular steel corrosion protection in acidic environment

The paper deals with the synthesis of Guar gum and ethyl acrylate (GG-EEA) composite. The synthesized natural polysaccharide composite was used as a corrosion inhibitor to reduce hydrogen evolution and P110 steel corrosion protection in 15% HCl (Hydrochloric acid). The primary corrosion techniques like weight loss, electrochemical impedance spectroscopy (EIS), and potentiodynamic polarization (PDP) was used to analyze the corrosion inhibition process. The PDP proposed that GG-EEA composite is a mixed-type corrosion inhibitor and inhibits corrosion by blocking the active sites presenting over the metal surface. The corrosion inhibition performance of GG alone is 77.5%, and that of GG-EEA is 92.3% at 500 mg/L. The adsorption of GG-EEA onto P110 steel is spontaneous and mixed type, i.e., both physical and chemical. The conformation of GG-EEA molecule adsorption was done using a scanning electron microscope (SEM), Energy dispersive x-ray spectroscopy (EDX), Atomic force microscopy (AFM), and X-ray photoelectron spectroscopy studies. Density functional theory (DFT) analysis was done to explore the active sites over the inhibitor in metal-inhibitor interaction. Molecular dynamic simulation (MD) simulations study reveals that GG-EEA has more adsorption capacity than GG alone.     

Inhibition effect of newly synthesized benzoxanthonesderivative on hydrogen evolution and Q235 steelcorrosion in 15% HCl under hydrodynamic condition: Combination of experimental,surface and computational study

The investigation of this study deals with the synthesis using green synthetic approach, characterization and application of benzoxanthones derivative namely 9,9-Dimethyl-12-p-tolyl-8, 9,10, 12-tetrahydrobenzo[a]xanthen-1-one (TBX) for the inhibition of Q235 steel corrosion in 15% HCl under dynamic condition. The results of EIS confirmed towards the increment in R_ct values with rise in concentration. Additionally, results of PDP reveals that TBX is cathodic type inhibitor. The maximum inhibitive excellency of TBX was given at 200 mg/L with the value of 92.3%. The increasing temperature tends to increase in corrosion rate. Langmuir adsorption isotherm provides the excellent fitting. The surface morphology and adsorption of TBX molecules were confirmed using scanning electron microscopy (SEM) and X-photo electron microscopy (XPS). Density functional theory (DFT) and Molecular dynamic simulation (MD) confirmed that corrosion inhibition efficiency ranking obtained for studied molecules is TBXH⁺> TBX.     

Insight of corrosion mitigation performance of SABIC iron in 0.5 M HCl solution by tryptophan and histidine: Experimental and computational approaches

The inhibitory strength of two amino acids namely, tryptophan (Tryp) and histidine (Hist) on the corrosion of SABIC iron (SABIC Fe) in a 0.5 M HCl solution was examined utilizing mass loss (MS), electrochemical (PDP and EIS) and theoretical studies. Density functional theory (DFT) and Monte Carlo (MC) simulation were inspected for Tryp and Hist inhibitors. All the corrosion parameters and theoretical data obtained from these studies confirm the inhibiting impact of the two amino acids. The efficacy of inhibition augment with augmentation the concentration of two amino acids from 100 to 500 ppm and reducing at elevated temperature. The effectiveness of the inhibition depends on the presence of some active centers that accelerate the adsorption process and the molar mass of the inhibitors. The inhibition efficacy of Tryp is greater than that of Hist reaching 92.09% at a concentration of 500 ppm while in the presence of Hist it is 89.37% using PDP measurements. Inhibition was demonstrated by spontaneous adsorption of Hist and Tryp on the surface of SABIC Fe according to the Langmuir adsorption isotherm. PDP curves clarified that the Tryp and Hist compounds acted as mixed type inhibitors. A variety of thermodynamic and kinetics parameters were computed and explained. SEM images demonstrate that the protective layer constructed on the surface of S– Fe in the presence of both amino acids. The results obtained from DFT are in complete agreement with the experimental work. Tryp and Hist compounds are adsorbed horizontally onto the surface of Fe (110).     

Corrosion inhibition performance of 4-(prop-2-ynyl)- [1,4]-benzothiazin-3-one against mild steel in 1 M HCl solution: Experimental and theoretical studies

4-(prop-2-ynyl)-2H [1,4]-benzothiazin-3(4H)-one (PBO) was synthesized and evaluated on corrosion resistance for mild steel (MS) in1 M HCl environment. The molecular and crystal structure of PBO has been determined by single-crystal X-ray crystallography, Hirshfeld surface (HS) analysis was carried out by using Crystal Explorer 17.5. Electrochemical impedance spectroscopy (EIS) and potentiodynamic polarization (PDP) techniques were used to find corrosion rate (CR) and corrosion inhibition efficiency (η) in the presence and absence of PBO. These techniques were supported with energy dispersive X-ray (EDX) and scanning electron microscope (SEM). Molecular Dynamics Simulation (MDS) and Frontier Molecular Orbital (FMO) are realized by means of the Density Functional Theory (DFT) method. The results show that PBO could offer an inhibition efficiency of 92% at 303 K. The type of inhibition mechanism of PBO was mixed-type. The Langmuir isotherm proved the highest compliance with experimental data, representing the generation of protective mono-layer of inhibitors on the MS substrate. The SEM pictures displayed a metallic substrate covered with a highly compact protective layer covered. The theoretical findings suggested by electronic/atomic computer simulations supported the inhibitive chemicals interfacial adsorption through reactive centres.     

Analysis of corrosion inhibition of Kleinhovia hospita plant extract aided by quantification of hydrogen evolution using a GLCM/SVM method

During a corrosion inhibition test, a combination of common electrochemical corrosion test methods with an in-situ quantification of H₂ evolution could provide a comprehensive analysis of the effectiveness of an organic inhibitor. This work analyzes the corrosion inhibition efficiency of Kleinhovia hospita plant extract on carbon steel specimens polarized in 1 M HCl, based on acquired H₂ bubbles images, by using gray level co-occurrence matrix (GLCM) and support vector machine (SVM) classification. A conformity was established between the classified-algorithm models and the corrosion test results obtained by potentiodynamic polarization test and electrochemical impedance spectroscopy. Hydrogen rate and corrosion rate show the same lowest trends at the addition of 3000 mg/L of KH extract. The inhibitor addition led to 99% of maximum inhibition efficiency. Based on the polarization data, KH extract is a mixed type inhibitor. Supported by Langmuir calculation for adsorption isotherm, a physisorption is stated as the main inhibition mechanism. The feature extraction using GLCM was able to distinguish changes in H₂ bubbles characteristics where the addition of inhibitor affected the corrosion rate. The GLCM/SVM method applied as a linear kernel function and showed 88% accuracy with d = 5 for image data testing. Remarkable changes in H₂ gas bubbles characteristic were observed in the specimen immersed in the solution with 3000 mg/L inhibitor addition, signified by 99% inhibition efficiency.     

Hydrogen generation during the corrosion of carbon steel in crotonic acid and using some organic surfactants to control hydrogen evolution

The purpose of this paper is to describe and evaluate the corrosion of carbon steel in crotonic acid for hydrogen production and using polysorbate 20 (NS), dioctyl sodium sulfosuccinate (AS) and benzalkonium chloride (CS) to control hydrogen evolution. Measurements were conducted in tested solutions using hydrogen evolution and electrochemical impedance spectroscopy (EIS) measurements and complemented by scan electron microscope (SEM) and energy dispersive X-ray (EDX) investigations. It is shown that the hydrogen generation rate obtained during the corrosion of carbon steel in crotonic acid increased with increase in acid concentration, temperature and immersion time. The addition of organic surfactants inhibits the hydrogen generation rate. The inhibition occurs through adsorption of organic surfactants on the metal surface. Adsorption processes followed the Langmuir isotherm. The order of effectiveness of the surfactants was AS > NS > CS. The values of activation energy (E_a) and heat of adsorption (Q_ads) were calculated and discussed.     

Corrosion inhibition, hydrogen evolution and antibacterial properties of newly synthesized organic inhibitors on 316L stainless steel alloy in acid medium

Electrochemical corrosion behavior and hydrogen evolution reaction of 316L stainless steel has been investigated, in 0.5 M sulfuric acid solution containing four novel organic inhibitors as derivatives from one family, using potentiodynamic polarization, electrochemical impedance spectroscopy (EIS) measurements and surface examination via scanning electron microscope (SEM) technique. The effect of corrosion inhibitors on the hydrogen evolution reaction was related to the chemical composition, concentration and structure of the inhibitor. The inhibition efficiency, for active centers of the four used compounds, was found to increase in the order: -Cl < -Br < -CH₃ < -OCH₃. The corrosion rate and hydrogen evolution using the compound with methoxy group as a novel compound was found to increase with either increasing temperature or decreasing its concentration as observed by polarization technique and confirmed by EIS measurements. The compound with methoxy group (newly synthesized) has very good inhibition efficiency (IE) in 0.5 M sulfuric acid (98.3% for 1.0 mM concentration). EIS results were confirmed by surface examination. Also, antibacterial activity of these organic inhibitors was studied. The results showed that the highest inhibition efficiency was observed for the compound that posses the highest antibacterial activity.     

Influence of cerium (III) ions on corrosion and hydrogen evolution of carbon steel in acid solutions

This paper intended to investigate the influence of rare earth Ce(III) ions on the corrosion behavior of carbon steel in two acid solutions (0.5 M HCl and 0.25 M H₂SO₄) in order to control the rate of hydrogen evolution in those systems. Potentiodynamic polarization and electrochemical impedance spectroscopy (EIS) tests were used for corrosion rate and electrochemical impedance evaluation. SEM was used to examine the sample surfaces immersed in acid solutions containing the optimal threshold Ce(III) concentration (0.1 mM). All results reveal that the corrosion resistance of carbon steel in HCl is superior to that in H₂SO₄ due to the higher rate of hydrogen production in the latter. A model for the corrosion process mechanism and inhibition by Ce(III) salt for carbon steel in the two tested media is proposed.     

Electrochemical and hydrogen evolution behaviour of a novel nano-cobalt/nano-chitosan composite coating on a surgical 316L stainless steel alloy as an implant

Herein, nanocomposite coatings consisting of chitosan (CSNPs) and cobalt nanoparticles (CoNPs) were deposited on bare 316L stainless steel alloy (316L SS) as a bone implant. Scanning electron microscope (SEM) and energy dispersive X-ray (EDX) were applied to characterize the morphological and chemical composition of the tested nanocoatings. In-vitro degradation and hydrogen evolution behaviour of the coated samples were examined by means of electrochemical impedance spectroscopy (EIS) and potentiodynamic polarization techniques, in Hank's solution containing of 1 × 10^?3 M calcium hydrogen phosphate drug at pH 7.4 and temperature 37 °C. This drug used as an inhibitor for protecting the alloy surface from the corrosive medium and minimized the hydrogen evolution rate. Results showed that the di-phasic coating (CoNPs-CSNPs) gave the highest electrochemical corrosion resistance with the lowest hydrogen evolution rate in comparison to the monophasic coatings (CS-NPs & Co-NPs). These corrosion results suggested that a CoNPs-CSNPs nanocomposite coating on 316L SS was effective for renewable or functional implants.     

Electrodeposition of conductive PAMT/PPY bilayer composite coatings on 316L stainless steel plate for PEMFC application

Stainless steel fulfills most of the requirements as bipolar plates in Proton Exchange Membrane Fuel Cell. However, it undergoes severe corrosion in fuel cell operating condition. This can be resolved by coating the stainless steel with corrosion resistive conducting polymers. In this study, homogeneous and adherent conductive Poly(2-amino-5-mercapto-1,3,4- thiadiazole)/Polypyrrole (PAMT/PPY) mono and bilayer polymer composite coatings are electrosynthesized on 316L SS in 0.5 M H₂SO₄ by cyclic voltammetry and chronopotentiometry. The hydrophobicity and surface morphology of the coatings are analyzed by contact angle and scanning electron microscopy respectively. The polymer coatings are evaluated in 0.5 M H₂SO₄ medium by potentiodynamic polarization and impedance techniques at 25 °C. The polarization results reveal that PAMT on PPY composite coating shifts the E_corr of the 316L SS towards noble direction. The EIS study reveals that the R_f value of PAMT on PPY coating is significantly higher by three orders (x10³ Ωcm²) of magnitude than uncoated 316L SS. The corrosion performance of the coatings in simulated PEMFC environment is investigated by potentiodynamic and potentiostatic studies. Results show that the PAMT on PPY and PPY on PAMT bilayer coatings are stable and increased the corrosion potential by about 410–470 mV and 275–310 mV (SCE) in simulated cathodic and anodic conditions respectively. This investigation reports that the PAMT on PPY bilayer coating is serving as a good physical barrier and protecting the 316L SS against corrosion in PEMFC environment.     

Influence of 2-(4-chlorophenyl)-2-oxoethyl benzoate on the hydrogen evolution and corrosion inhibition of 18 Ni 250 grade weld aged maraging steel in 1.0 M sulfuric acid medium

Electrochemical corrosion behavior and hydrogen evolution reaction of weld aged maraging steel have been investigated, in 1.0 M sulfuric acid solution containing different concentrations of 2-(4-chlorophenyl)-2-oxoethyl benzoate (CPOB). The data obtained from polarization technique showed that the corrosion current density (i_corr) and the hydrogen evolution rate decrease, indicating a decrease in the corrosion rate of weld aged maraging steel as well as an increase in the inhibition efficiency (η%) with the increase in inhibitor concentration. Changes in impedance parameters were indicative of adsorption of CPOB on the metal surface, leading to the formation of protective film. Both activation (E_a) and thermodynamic parameters (ΔG_ads⁰, ΔH_ads⁰ and ΔS_ads⁰) were calculated and discussed. The adsorption of CPOB on the weld aged maraging steel surface obeyed the Langmuir adsorption isotherm model. Scanning electron microscopy (SEM) and energy dispersive X-ray spectroscopy (EDS) study confirmed the formation of an adsorbed protective film on the metal surface.     

Electrochemical study of perlite-barium ferrite/conductive polymer nano composite for super capacitor applications

Polyaniline/perlite-barium ferrite nanoparticles (PANI/PBF-NPs) composite electrodes were studied in here for super capacitor applications. The PBF-NPs synthesized using hydrothermal technique and then the composite electrode was fabricated electrochemically by cyclic voltammetry (CV) technique. Transmission electron microscopy (TEM), Scanning electron microscopy (SEM), X-ray diffraction (XRD), Brunauer-Emmett-Teller nitrogen adsorption/desorption (BET) and fast Fourier transform infrared spectroscopy (FTIR) were employed to study the morphological and structural properties of the prepared electrodes. Furthermore, various electrochemical techniques were used such as CV, Galvano static charge-discharge (GCD) and electrochemical impedance spectroscopy (EIS) to investigate their electrochemical performance as well. SEM graphs show uniform distribution of 60-nm PBF-NPs in the PANI filaments. The specific capacitance of PANI and composite electrodes was obtained to be 225 and 330 F/g, respectively. In addition, inclusion of PBF-NPs in the structure of PANI electrode had significantly increased the conductivity of composite electrodes. Continuous charge-discharge cycles test illustrated the good capability of this nano composite material for use as a charge storage device.     

Appraisal of corrosion inhibiting ability of new 5-N-((alkylamino)methyl)quinolin-8-ol analogs for C40E steel in sulfuric acid

Two new 5-N-((alkylamino)methyl)quinolin-8-ol analogs, namely 5,5'-(azanediylbis(methylene))bisquinolin-8-ol (ABMQ), 5-(((4-hydroxybenzyl)amino) methyl)quinolin-8-ol (HAMQ) were synthesized in moderate yields via the N-alkylation of 5-Aminomethyl-quinolin-8-ol with benzyl alcohol derivatives. Their structures were determined on the basis of elemental analysis, NMR, and FT-IR. The corrosion inhibiting ability of 5-N-((alkylamino)methyl)quinolin-8-ol analogs was assessed on C40E steel in 0.5 M H₂SO₄ media via multiples approaches such that the weight reduction, electrochemical measurements, UV–Visible spectroscopy, scanning electron microscopy (SEM), and computational techniques. All achievements are underscored that ABMQ and HAMQ behave as good corrosion inhibitors of C40E steel in sulfuric acid and their performances follow the sequence, ABMQ (97.3) > HAMQ (94.6) at 0.001 M. Both 5-N-((alkylamino)methyl)quinolin-8-ol analogs revealed mixed-type inhibitory activity. Two loops; one in high-frequency and another in low-frequency were observed in EIS plots. A substantial reduction of corrosive attack on the surface exposed to ABMQ or HAMQ solution was upheld by SEM. The 5-N-((alkylamino)methyl)quinolin-8-ol analogs were chemisorbed on the C40E steel surface and followed the Langmuir isotherm model. Quantum chemical calculations using the Density Functional Theory (DFT) method and molecular dynamics simulations suggest a good agreement with the experimental results.     

Investigation on the corrosion resistance of carbon black-graphite-poly(vinylidene fluoride) composite bipolar plates for polymer electrolyte membrane fuel cells

The goal of the present work was to evaluate the corrosion resistance of carbon black (CB)-synthetic graphite (SG)-poly(vinylidene fluoride) (PVDF) composites using electrochemical impedance spectroscopy (EIS) and potentiodynamic polarization curves. The tests were conducted in 0.5 M H₂SO₄ + 2 ppm HF solution at 70 °C to simulate the typical environment of polymer electrolyte membrane fuel cells. The fracture surface of the specimens was characterized by scanning electron microscopy. The through-plane electrical conductivity was also determined. The corrosion resistance decreased as the carbon black content increased up to 5 wt.%. The highest electrical conductivity was achieved for the composition CB = 5 wt.%, PVDF = 15 wt.%, SG = 80 wt.%. A detailed discussion of the EIS data is given. This approach is unprecedented in the current literature. EIS has proven to be a valuable tool to the design of electrically efficient bipolar plates.     

Electrocatalytic performance of carbon dots/palladium nanoparticles composite towards hydrogen evolution reaction in acid medium

In this work, nitrogen doped carbon dots (NDCDs) and nitrogen doped carbon dots supported palladium nanoparticles composite (n-Pd@NDCDs) were synthesized through hydrothermal carbonization and thermolytic reduction using Morinda citrifolia (M. citrifolia) fruit and palladium chloride as carbon and Pd precursors, respectively. The synthesized materials viz., n-Pd@NDCDs and NDCDs were duly characterized by high resolution transmission electron microscopy (HR-TEM), Raman spectroscopy, X-ray photoelectron spectroscopy (XPS), X-ray diffraction (XRD), and Fourier transform infrared spectroscopy (FT-IR). The optical properties of NDCDs were studied by ultraviolet visible (UV–Vis), and fluorescence spectroscopy techniques. Further, the electrocatalytic hydrogen evolution reaction (HER) performance of n-Pd@NDCDs was evaluated by linear sweep voltammetry (LSV), Tafel, and electrochemical impedance spectroscopy (EIS) measurements in 0.5 M aqueous H₂SO₄. The onset potential of n-Pd@NDCDs was about −0.195 V_RHE, which was lower than NDCDS (−0.392 V_RHE) and bare glassy carbon (−0.603 V_RHE). The calculated Tafel slope values of n-Pd@NDCDs were 135 and 141.8 mV/dec, from the voltammetric and EIS methods, respectively. Moreover, the n-Pd@NDCDs exhibited small overpotential of 0.291 V to attain a current density of 10 mA/cm². The EIS studies revealed that the HER charge transfer resistance was dropped from 84.3 to 18.3 Ω/cm² while increasing of potential, which revealed good conductivity and electrocatalytic activity of n-Pd@NDCDs. Thus the present work vouched for the candidature of n-Pd@NDCDs as an effective electrocatalyst for the HER in acidic medium.     

Influence of heat treatment on corrosion behaviors of 316L stainless steel in simulated cathodic environment of proton exchange membrane fuel cell (PEMFC)

The influences of two types of heat-treatments on the corrosion behavior of 316L SS in the simulated cathodic environment of PEMFC, are investigated using potentiodynamic curve, electrochemical impedance spectroscopy (EIS), Mott-Schottky plot and auger electron spectroscopy (AES), respectively. The results show that 316L SS is in the passive state within the potential region from −0.1V_SCE to 0.8V_SCE in the simulated cathodic environment of PEMFC, and a passive film can be formed on 316L SS. The passivity of 316L SS in the simulated cathodic environment of PEMFC firstly increases and then degrades with the increased solid solution temperature or time, and the best passivity corresponds to the solid solution temperature at 1050 °C for 40 min among other solid solution treatments. While 316L SS heat-treated with the solid solution treatment at 1050 °C for 40 min plus aging treatment at 900 °C for 4 h, also has the best passivity in the same solution among other solid solution plus aging treatments. The best corrosion protection, lowest donor density and the highest thickness of the passive film corresponding to the solid solution temperature at 1050 °C for 40 min among other solid solution or solid solution plus aging heat treatments, and this treatment is mostly suitable for improving the anti-corrosion property of 316L SS in the simulated cathodic environment of proton exchange membrane fuel cell (PEMFC).     

Corrosion inhibition of methanol towards stainless steel bipolar plate for direct formic acid fuel cell

The corrosion properties of AISI316L stainless steel (316 L SS) as bipolar plates are investigated under aqueous acid methanol solutions (0.05 M H₂SO₄ + 2 ppm HF + 10 M HCOOH + x M CH₃OH (x = 0, 3, 6 and 9) solutions at 70 °C) to simulate the varied anodic operating conditions of direct formic acid fuel cells (DFAFCs). When the methanol content is higher, the potentiodynamic, potentiostatic polarisation and EIS tests of the 316 L SS bipolar plates all show excellent corrosion resistance. The surface morphology and the glow discharge mass spectrometer (GDMS) illustrate that the surface corrosion on 316 L SS bipolar plates is slowed down when the methanol concentration is increased. These results indicate the methanol plays the role in retarding the corrosion rate of the 316 L SS in simulated DFAFCs anodic operating conditions by restricting the proton conductivity in the test solutions. The sample tested in higher content methanol solution has smoother corroded surface and thinner passivation film, which contributes to a lower interfacial contact resistances (ICR) value.     

Immersion corrosion behavior,electrochemical performance and corrosion mechanism of subsonic flame sprayed FeCoCrMoSi amorphous coating in 3.5% NaCl solution

A FeCoCrMoSi amorphous coating (AC) was fabricated on Ti6Al4V alloy (TA) by subsonic flame spraying (SFS) technique, which was used to improve its corrosion resistance. The morphology, element distribution and chemical composition of obtained coating were analyzed using a scanning electron microscope (SEM), energy dispersive spectroscopy (EDS) and X–ray Fluorescence (XRF), respectively, and its amorphous structure was confirmed by X–ray diffraction (XRD). The immersion corrosion behavior and electrochemical performance of FeCoCrMoSi AC immersed in 3.5% NaCl solution for the different days were systematically investigated, and the corrosion mechanism of amorphous structure was also discussed by the model of passive film. The results show that the FeCoCrMoSi AC exhibits the dense amorphous structure, which is beneficial to improving the anti–corrosion performance of TA. The potentiodynamic polarization curve (PPC) and electrochemical impedance spectroscopy (EIS) indicate that the FeCoCrMoSi AC with the lowest i_corr of 1.479 × 10^?6 A·cm^?2 immersed for 60 days has the largest capacitor loop diameter of 7.53 × 10⁵ and charge transfer resistance R_ct of 4.31 × 10⁴ Ω, showing the highest comprehensive corrosion resistance. The mechanism of corrosion resistance is contributed to the Cr–rich passive film, which is further stabilized by the addition of Mo.     

Promoting formic acid and ethylene glycol electrooxidation activity on Ga modified Pd based catalysts

Herein, carbon nanotube (CNT)-supported Ga@PdAgCo catalysts were synthesized by sodium borohydride (SBH) sequential reduction method. These catalysts were characterized by X-ray diffraction (XRD), transmission electron microscopy (TEM), X-ray photoelectron spectroscopy (XPS), and inductively coupled plasma-mass spectrometry (ICP-MS). Characterization results revealed that these catalysts were succesfully preared at desired loading and atomic ratios. From the XRD pattern, the crystallite size of 0.5% Ga@PdAgCo(80:10:10)/CNT catalysts was found as 6.95 nm by utilizing the Scherrer equation. From TEM measurements, the average particle sizes of Pd/CNT, PdAgCo(80:10:10)/CNT, and 0.5% Ga@PdAgCo(80:10:10)/CNT catalysts were found to be 54 nm, 25 nm, and 7 nm, respectively. It is clear that particle sizes obtained from TEM and XRD were close to eachother. Electrochemical impedance spectroscopy (EIS), chronoamperometry (CA), and cyclic voltammetry (CV) measurements were realized to examine the formic acid and ethylene glycol electrooxidation performances of catalysts. 0.5% Ga@PdAgCo(80:10:10/CNT) and 7% Ga@PdAgCo(80:10:10/CNT) catalysts had the best specific activity and mass activity as 3.37 mA/cm² (297.61 mA/mg Pd) and 4.95 mA/cm² (462.59 mA/mg Pd) for ethylene glycol and formic acid electrooxidation, respectively. In addition, EIS results showed that Ga@PdAgCo(80:10:10/CNT) catalyst had a faster electron transfer rate via low charge transfer resistance. As a result, 0.5% Ga@PdAgCo(80:10:10/CNT) catalyst is a promising new anode catalyst for direct ethylene glycol fuel cells.     

Inhibitive effect of onion mesocarp extract-nickel nanoparticles composite on simultaneous hydrogen production and pipework corrosion in 1 M HCl

Nanoscale nickel is prepared from ethanol extracts of Allium cepa and characterized. Zerovalent face centred cubic (fcc) nickel nanoparticles oriented mainly at Ni (111) plane formed rapidly within 30–45 min. The nanoparticles are stabilized by negative surface potential, non-agglomerated, monodispersed, round-shaped and distributed between sizes of 39.5–53.1 nm. The nanoparticles are used to simultaneously regulate the rates of hydrogen gas production and X80 steel corrosion in 1 M HCl solution for the first time. The nanoparticles efficiently inhibit hydrogen gas evolution and X80 steel corrosion rates especially at increased concentration. Inhibition efficiency increases as temperature increases from 303 to 323 K, remains fairly constant from 323 to 343 K and decreases drastically from 343 to 363 K. By means of O–H, N–H and C=C sites, the nanoparticles are spontaneously physically adsorbed on X80 steel surface and act as mixed type corrosion inhibitor with dominant influence on cathodic reaction involving hydrogen gas evolution. In the presence of the nanoparticles, surface roughness (measured by AFM) reduces by 76.0% and heights of peaks from the mean plane reduces by 58.2%. Comparatively, even 100 ppm of the nanoparticles showed higher inhibition efficiency at all temperatures than 1000 ppm concentration of the crude extract.