HCl Solution Research Articles

Fabrication of a bimodal micro/nanoporous copper cladding layer by the high-speed laser cladding and dealloying

The Cu30Mn70 cladding layer was prepared by high-speed laser cladding technology and successfully combined with chemical dealloying method to prepare a bimodal micro/nanoporous copper coating. The 0.1 M HCl solution was experimentally determined as the dealloying solution. During the dealloying, the Mn-rich regions were preferentially corroded and formed micron pores in situ; the remaining regions served as a framework to form nanoporous structures on both sides. With increasing time, the transformation of the nanoporous structure led to micron ligaments thinning or fracture, resulting in the structural collapse of the bimodal microporous/nanoporous copper coating surface. Repeated oxidation-dissolution processes on the surface accelerate the structural collapse of the surface and inhibit the demanganization layer thickness growth. The same structure was formed in the cross-sectional direction, with no structural collapse due to continuous H+ consumption and low corrosivity in the micropores. The bimodal microporous/nanoporous copper coatings remained highly porosity and rapidly increased in thickness to 340 μm from 24 to 72 h. After 72 h, the surface structure started to collapse and the growth of the demanganization layer thickness slowed down.

Corrosion behavior of novel Ti6422 alloy with equiaxed structure and lamellar structure in HCl solution

This study systematically investigated the electrochemical corrosion and static immersion corrosion behavior of the novel Ti6422 (Ti-6Al-4V-2Mo-2Fe) alloy with equiaxed (EM) and lamellar structure (LM) in HCl solution. The differences in corrosion performance between EM and LM samples were analyzed based on the characteristics of the passive film and substrate microstructure. Results indicated that the LM sample contained higher contents of TiO₂, Al₂O₃, and MoO₃ with higher stability compared with the EM sample, and the thickness of passive film was approximately twice that of the EM sample. Additionally, the donor density of LM sample was lower than EM sample. These findings indicate that the passive film on LM samples is thicker, with fewer defects and higher density. Electrochemical corrosion results revealed that the corrosion current of LM samples was lower and the polarization resistance was higher than these of EM samples, both suggesting superior corrosion resistance of LM samples. Immersion corrosion further confirmed that the LM sample had a lower corrosion rate. The enhanced corrosion resistance in LM samples was primarily due to higher content of corrosion-resistant β phase. Conversely, the numerous micro-galvanic cells between αs precipitates and adjacent β phase in EM samples weakened the corrosion resistance. Overall, these results demonstrated that regulating microstructure through heat treatment is an effective strategy for improving corrosion resistance of titanium alloys.

Pharmaceutical salt of isoniazid−orotic acid with optimized solubility, dissolution rate, and tabletability

Isoniazid (INH) is a first-line antitubercular drug characterized by its high solubility and rapid absorption following oral administration, which poses challenges in maintaining sustained therapeutic concentrations. To address this issue, we have developed a novel pharmaceutical salt of INH with orotic acid (OA). Single-crystal X-ray diffraction (XRD) analysis revealed that intermolecular proton transfer occurs between the carboxyl group of OA and the pyridine nitrogen site of INH, resulting in a salt comprising INHH+ cations and OA− anions. Solubility and dissolution studies indicated that INH−OA exhibits significantly reduced solubility and decelerated intrinsic dissolution rate (IDR). Specifically, solubility reductions were observed to be 74.24% in pH 1.2 HCl solution and 90.29% in pH 6.8 phosphate buffer solution. The IDR of the salt was found to be 2.62% and 0.96% of that of pure INH in pH 1.2 and pH 6.8 aqueous media, respectively. Additionally, INH−OA demonstrated improved tabletability. These findings suggest that the formation of this salt significantly enhances the pharmaceutical properties of INH.

Experimental and theoretical simulations to examine the influence of nonionic surfactant on the corrosion control of mild steel in hydrochloric acid

The increasing demand for corrosion prevention strategies that are both effective and sustainable is part of the research the background. Nonionic surfactants offer a potential replacement for traditional corrosion inhibitors. These surfactants are well-known for their low toxicity and biodegradability. The research involved conducting experimental tests (such as weight loss, polarization and impedance spectroscopy) and theoretical computations to investigate the role of nonionic surfactant (polyoxyethylene (7) tribenzyl phenyl ether) (PETPE) in controlling the corrosion of mild steel in hydrochloric acid (1.0 M HCl) environment. The results of the study demonstrated that PETPE exhibited significant corrosion inhibition properties for mild steel in HCl solution. The inhibition efficiency of PETPE was found to increase with increasing PETPE concentration. PETPE is an excellent corrosion inhibitor because it significantly reduces the rate of corrosion, as seen by the notable inhibition efficiency result (95.4%) at a relatively low dose of PETPE (100 ppm). Thermodynamic studies were used to discuss the fundamental mechanisms that control PETPE-acid interactions. The adsorption process followed Langmuir adsorption isotherm, indicating a monolayer adsorption of the PETPE on the mild surface. Theoretical computations confirm the strong inhibition behavior of PETPE. The innovative feature of this research is its comprehensive strategy, which integrates experimental studies and theoretical simulations to evaluate the impact of PETPE on the corrosion control of mild steel in hydrochloric acid. The combined effort has the ability to supply valuable knowledge into the mechanisms of corrosion that will lead to the establishment of powerful corrosion control strategies.

Preparation process, surface properties and mechanistic study of HVAF-sprayed CoCrFeNiMo0.2 high-entropy alloy coatings

The objective of this study is to develop infrared reflective coatings with excellent service performance in extreme environments, aimed at reducing system energy consumption and enhancing service life. In this work, CoCrFeNiMo0.2 high-entropy alloy (HEA) powder was deposited on the 316 L stainless steel (SS) substrate using High-Velocity Air Fuel (HVAF) thermal spray technology. The microstructure, mechanical properties, infrared reflectivity, and corrosion resistance of the coatings under different spraying parameters were investigated and compared with those of the substrate. Computational Fluid Dynamics (CFD) simulation was employed to analyze the influence of HVAF spraying parameters on flame characteristics and particle flight behavior, providing guidance for optimizing the spraying process and explaining underlying mechanisms. Results demonstrated that adjusting parameters such as propane and air pressure, spraying distance, and powder feed rate could produce dense coatings with <1 % porosity. The microhardness of the coatings was approximately 1.8 times that of the substrate, and the bonding strength between the coating and the substrate is increased to 39.4 MPa. Additionally, the near-infrared reflectivity of the coatings was significantly higher than that of the substrate, with an enhancement of 18.7 %. Coatings sprayed under different parameters exhibited superior passivation and pitting corrosion resistance compared to the substrate in 3.5 wt% NaCl and 1 mol/L HCl solutions. Optimization of spraying parameters further enhanced the protective capability of the passivation film and corrosion resistance. Consequently, CoCrFeNiMo0.2 HEA coatings prepared by HVAF spraying technology demonstrate excellent comprehensive performance, holding promising potential for industrial applications.

Preparation of modified silica gel supported silver nanoparticles and its evaluation using zone of inhibition for water disinfection

In this work, preparation of modified silica gel supported silver nanoparticles and its evaluation using zone of inhibition for water disinfection were investigated. The silica contents of the teff straw [TS] and teff straw ash [TSA] are 5.92 and 92.21 %, respectively. The calcinated TS ash at 700 °C was mixed with NaOH solution. The solution is then neutralized with HCl solution and then gel formation using the sol gel method. The silica gel yield was recorded and characterized. The SG with major silica functional group, amorphous structure, high porosity from the morphology, high surface area of 807.163 m2/g, pore volume of 0.34 cm3/g, pore diameter of 1.70 nm and silica gel purity of 99.39 % were achieved at a calcination temperature of 700 °C. It is then; further modified using trimethylchlorosilane (TMCS)/ethanol/hexane at different volumetric ratio and the resulting product is modified silica gel (MSG). MSG has excellent hydrophobic properties that have been required during water treatment. In this method, MSG with a major silica functional group, well ordered structure due to the TMCS modifier, maximum surface area of 510.40 m2/g was achieved at volumetric ratio of 0.25:0.25:1 of TMCS/ethanol/hexane, respectively. Then, MSG supported AgNPs (MSG-AgNPs) was prepared by mixing different concentrations of AgNPs-MSG and characterized. The MSG-AgNPs have shown AgNPs on the surface of MSG from the EDX result, different absorbance, pore from the morphology, with a maximum surface area of 475.0 m2/g was obtained at 1.5 mM of AgNPs concentrations. The performance of MSG-AgNPs was evaluated using zone of inhibition measurement and batch disinfection studies against E. coli and S. aureus. At 1.5 x 108 CFU/mL initial bacterial concentrations, the maximum inhibition zone diameter was 12.80 and 14.30 mm for E. coli and S. aureus, respectively.

Synthesis, Characterization, Theoretical, and evaluation of Eco-Friendly benzimidazolylmethyl-pyrazole carboxylate Schiff Bases corrosion inhibitors for mild steel

In this study, benzimidazolylmethyl-pyrazole carboxylate derivatives were synthesized via a 1,3-dipolar cycloaddition reaction and characterized using IR, HRMS and NMR spectroscopy. Three derivatives, namely ethyl 5-((3-(cyclohex-1-en-1-yl)-2-oxo-2,3-dihydro-1H-benzo[d]imidazol-1-yl)methyl)-1-phenyl-1H-pyrazole-3-carboxylate (Ph-BPC), ethyl 5-((3-(cyclohex-1-en-1-yl)-2-oxo-2,3-dihydro- 1H-benzo[d]imidazol-1-yl)methyl)-1-(p-tolyl)-1H-pyrazole-3-carboxylate (CH3Ph-BPC), and ethyl 1-(4-chlorophenyl)-5-((3-(cyclohex-1-en-1-yl)-2-oxo-2,3-dihydro-1H-benzo[d]imidazol-1-yl)methyl)-1H-pyrazole-3-carboxylate (ClPh-BPC), were evaluated as corrosion inhibitors for mild steel (MS) in a 1 M HCl solution. Potentiodynamic polarization (PDP) and electrochemical impedance spectroscopy (EIS) measurements revealed high inhibition efficiencies of 98.5 %, 98.2 %, and 97.7 % for ClPh-BPC, Ph-BPC, and CH3Ph-BPC, respectively, at a concentration of 10-4 M. Scanning electron microscopy (SEM), energy-dispersive X-ray (EDX) and X-ray diffraction (XRD) analyses confirmed the formation of protective surface layers, significantly reducing corrosion rates. Thermodynamic analysis indicated that the adsorption of these inhibitors follows the Langmuir isotherm model with adsorption energies of −50.12 kJ/mol for ClPh-BPC, −50.52 kJ/mol for Ph-BPC, and −51.62 kJ/mol for CH3Ph-BPC, suggesting chemisorption. Computational studies, including Monte Carlo (MC), density functional theory (DFT), and molecular dynamics (MD) simulations, showed strong agreement with experimental results, further validating the adsorption behavior and corrosion inhibition mechanisms of these compounds.

Comprehensive Study on the Corrosion Inhibition of Aluminum in HCl by N1, N1'-(Ethane-1,2-diyl)di(ethane-1,2-diamine): Experimental and Theoretical Approaches

The inhibitory effects of the novel molecule N1, N1'-(ethane-1,2-diyl)di(ethane-1,2-diamine) (TETA) on aluminum (Al) corrosion were investigated in 0.2, 0.3, and 0.4 M HCl solutions. Electrochemical impedance spectroscopy (EIS), potentiodynamic polarisation (PDP), quantitative techniques, and surface morphology characterisation were utilised. Surface morphology characterisation via atomic force microscopy (AFM) and scanning electron microscopy with energy-dispersive X-ray spectroscopy (SEM/EDS) confirmed the efficacy of the inhibitor in preventing corrosion. Weight loss research revealed that the protective efficacy of TETA grows with increasing concentration but shrinks with increasing temperature of the acidic solution. The findings indicate a marked increase in inhibition efficiency as TETA content rises, reaching 99.0 % when measured by the weight loss method, 98.34% through EIS, and 94.13% via electrochemical polarization. Polarization curves show that TETA stops hydrochloric acid from acting on the anodic type. Both the charge-transfer resistance and the double-layer capacitance decrease with increasing inhibitor concentration, as shown by the adsorption mechanism and supported by the EIS results. "The Langmuir isotherm and negative Gibb's free energy values demonstrate that the inhibitor molecules cling to the metal and that they adsorb to the aluminium spontaneously. In addition to analysing TETA via density functional theory (DFT), the adsorption of TETA on the surface of aluminium (Al) was examined via molecular dynamics (MD) simulations. The results show that the TETA molecule successfully blocks the corrosion process.

Theoretical and experimental studies on the electrochemical behavior of steel in HCl solution in the presence of two bio-inhibitor mixtures

In this new study, the inhibitory effectiveness of two bio-inhibitor mixtures has been studied on the corrosion characteristics of carbon steel in an HCl environment. The inhibitors were derived from a plant seed (quinoa seed-QS) and an insect extract (Oestrus ovis larvae-OOL). The total inhibitor concentration was a variable factor even the ratio of bio-inhibitor concentration was a fixed parameter. The electrochemical behavior of steel substrate was investigated through the Tafel polarization and electrochemical impedance spectroscopy measurements. Fourier transform infrared spectroscopy and field emission scanning electron microscopy were performed to identify bonds and analyze the morphology of the corroded surface of the steel. Additionally, molecular dynamics (MD) simulation and quantum calculations were applied to investigate the inhibitory influence of utilized bio-inhibitors. The experimental results indicated that the corrosion resistance decreased to 85 % when the optimum total concentration of the bio-inhibitor was 1 g L−1. The Langmuir model was used to illustrate the adsorption mechanism on the steel surface when physical adsorption occurred. Quantum chemical calculations revealed that the QS-inhibitor adsorbed more effectively onto the metal surface than the OOLE-inhibitor, due in part to a lower energy gap and higher HOMO energy. MD simulation and Monte Carlo calculations further confirmed that the QS-inhibitor was adsorbed on the Fe (110) surface with higher adsorption energy than the OOLE-inhibitor.

A robust polymetallic-coated sheathless interface with high acid and alkali resistance for coupling capillary electrophoresis with mass spectrometry

A robust interface for coupling capillary electrophoresis (CE) to mass spectrometry (MS) was critical to maintain high separation efficiency of CE while achieving high sensitivity of MS. Current interfaces often suffer from problems such as reproducibility and ruggedness. For this purpose, a new polymetallic-coated sheathless interface was developed for the coupling of CE with MS. The electrical contact of the interface was achieved by etching one end of the fused silica capillary into a tapered tip using hydrofluoric acid (HF) solution, and then depositing a thin layer of chromium followed by a layer of platinum on it via physical vapor deposition technique. The performance of the new sheathless interface was systematically evaluated for the effect of flow rate and electrospray ionization (ESI) voltage on MS signal intensity, as well as the sample loading volume on CE separation efficiency and repeatability by using peptide standards and tryptic digest of bovine serum albumin (BSA). The interface was capable of generating stable electrospray even at ultra-low flow rate of 12.2 nL/min. In addition, the acid and alkali resistance of the polymetallic- coated emitter was tested by immersing it into 1M HCL and 1M NaOH solution, respectively. The results showed that polymetallic coating was still intact even after continuous immersion in the alkaline solution for 8 days (192 h) and a longer period in the acidic solution, indicating its excellent chemical stability. All the experimental results indicated that the sheathless interface fabricated by the new method in this study was robust and stable, making it promising for both sensitive and robust CE-MS sample analysis.

Preparation and structural characteristics of polysaccharides from loquat peel waste, and their preliminary bioactivities.

Loquat peel, often as food waste, is a valuable source of bioactive polysaccharides. However, study of such polysaccharides is insufficient, leaving a significant gap in understanding their preparation, structure and bioactivities. In this study, three types of loquat peel polysaccharides (LPWP, LPHP and LPNP) were sequentially extracted using hot water, HCl and NaOH solutions, respectively. Among them, LPWP was the purest, with a yield of 3.4% and molecular weight of 470.6 kDa, and it differed from LPHP and LPNP in structure, as evidenced by Fourier transform infrared spectroscopy, X-ray diffraction and scanning electron microscopy, which demonstrated that LPWP consisted of more arabinose (Ara) but less galacturonic acid, rhamnose and galactose, with molar percentages of 71.3%, 23.3%, 3.5% and 1.9%, respectively. Besides, LPWP also exhibited superior antioxidant and antihyperglycemic activities in vitro, particularly in inhibiting α-amylase and α-glucosidase. Methylation and nuclear magnetic resonance analysis confirmed that LPWP was a methyl-esterified pectic polysaccharide rich in branched arabinan, as evidenced by the notable proportion of α-Ara residues, including T-α-Araf, 1,5-α-Araf and 1,2,3,5-α-Araf, with molar percentages of 27.1%, 23.1% and 10.2%, respectively. AFM imaging further revealed its branched-chain morphology and aggregation behavior. This study highlights the potential of loquat peel polysaccharides as a bioactive ingredient with significant antioxidant and antihyperglycemic properties, particularly LPWP, which was found as a methyl-esterified pectic polysaccharide with abundant-branched arabinan. Our work provides valuable insights into the application of loquat peel polysaccharides in functional foods. © 2024 Society of Chemical Industry.

Exploring the Corrosion Potential of Three Bio-Based Furan Derivatives on Mild Steel in Aqueous HCl Solution: An Experimental Inquiry Enhanced by Theoretical Analysis.

This research deals with the corrosion inhibition of mild steel in a highly corrosive aqueous HCl medium with a concentration of 0.5 M, using three different corrosion inhibitors: furan-2-carboxylic acid (1), furan-2,5-dicarboxylic acid (2), and furan-2,5-diyldimethanol (3). Various electrochemical tests, such as potentiodynamic polarization (PP or Tafel curve) and electrochemical impedance spectroscopy, were systematically performed. The experimental results underscore the remarkable corrosion mitigating properties of inhibitors 1-3 on mild steel, showing inhibition efficiencies of 97.6, 99.5, and 95.8%, respectively, at a concentration of 5 × 10-3 M and temperature T = 298 K. Notably, the inhibition efficiency of each inhibitor 1-3 shows a positive correlation with its concentration. In addition, consistent results from all electrochemical methods confirm that 1-3 act as mixed inhibitors. These findings remain robust across different experimental techniques, ensuring the reliability and comprehensiveness of the results. Theoretically, the inhibitors were optimized using the Density Functional Theory/B3LYP/6-311++G(d,p) method in gas and aqueous phase to evaluate their reactivity and stability. Among them, compound 2 stands out for its enhanced reactivity and stability, highlighted by optimal EHOMO and ELUMO values. Negative electrostatic potential mapping suggests potential reaction centers, while Fukui functions reveal localized sites of reactivity, supported by a favorable electronic distribution and specific interactions with metal surfaces. Reduced density gradient analysis also confirms the suitability of this compound for noncovalent interactions, in agreement with experimental data.These theoretical results are in good agreement with experimental data, confirming the excellent performance of compound 2 as a corrosion inhibitor.

Direct response of liquid crystal to pH changes for wide range pH sensing via the whispering gallery mode.

pH sensing is essential in various fields including healthcare, environmental monitoring, food safety, and agriculture. In this Letter, we propose a method for a wide-range pH measurement based on the direct response of liquid crystal (LC) to pH variations via the whispering gallery mode (WGM). The liquid crystal 4-cyano-4'-pentylbiphenyl (5CB) is selected for its excellent optoelectronic properties and the birefringence of 5CB microdroplets serving as spherical resonators. This sensor achieves wide-range pH sensing without any intermediaries. Polarized optical microscopy (POM) and WGM provide a qualitative morphological analysis and accurate quantitative spectral measurements. Under alkaline conditions (pH 7.6 to 13.3), POM images of 5CB microdroplets show a complete transition from bipolar to radial structures, with an average sensitivity of 1.78 nm/pH of redshift in WGM spectra. In acidic conditions (pH 6.65 to 1.5), structural changes observed by POM are minor, with a sensitivity of 1.06 nm/pH of blueshift in WGM spectra. This difference is attributed to the varying refractive indices of HCl and NaOH solutions. This method offers a reference for theoretical studies on pH and LC interactions and holds promise for the development of LC-based pH sensors.

Investigating the corrosion inhibition properties of a Schiff base on mild steel in HCl solution: experimental and theoretical insights

Investigating the corrosion inhibition properties of a Schiff base on mild steel in HCl solution: experimental and theoretical insights

Synthesis and investigation of novel sulfonamide-1,2,3-triazoles corrosion inhibitors for E24 steel in 1 M HCl solution: A combination of modeling and experimental approaches

Synthesis and investigation of novel sulfonamide-1,2,3-triazoles corrosion inhibitors for E24 steel in 1 M HCl solution: A combination of modeling and experimental approaches

Utilizing rice husk-derived Si/C composites to enhance energy capacity and cycle sustainability of lithium-ion batteries

Traditional graphite anodes have a specific capacity of approximately 372 mAh/g, whereas silicon presents a promising alternative with theoretical capacities reaching up to 4200 mAh/g. However, substantial volumetric changes in silicon during lithiation lead to rapid degradation of capacitance. This study explores the utilization of rice husk, an abundant agricultural waste, as a raw material for Si/C composites. Rice husk inherently contains significant amounts of silicon and carbon, rendering it a sustainable and economical source. The activated carbon was derived from rice husk by carbonization and thermochemically activation with activation temperature of 850 °C and KOH agent. The silicon dioxide was derived from rice husk by subjecting to annealing in a muffle furnace at 650 °C for 4 h following NaOH and HCl solution treatment. The silicon was derived from silicon dioxide by thermomagnesium treatment in a tube furnace at 700 °C for 120 min. SEM, elemental analysis, XRD, Raman, and FT-IR were used to characterize the materials to evaluate their morphological and structural composition. Electrochemical performance evaluation demonstrated improved energy capacity and stability, highlighting rice husk-derived Si/C composites as a viable solution for advancing lithium-ion battery performance. This innovative approach not only lowers production costs but also supports sustainable development by effectively utilizing agricultural waste.

Inhibitive Effect of Mangifera Indica Extract on Mild Steel in Hydrochloric Acid Solution

This research investigated the corrosion inhibition potential of Mangifera Indica Peel Extract (MIPE) for mild steel in a 1 M HCl solution. The study explored the effects of extract concentration, solution temperature, and immersion time on the inhibition potential of MIPE using weight loss measurements at extract concentrations of 0, 1.0, 1.5, and 2.0 g/L, temperatures of 303 K and 323 K, and immersion times of 1, 2, 4, 6, and 8 h. Experimental results showed that MIPE significantly reduced the corrosion rate of mild steel, with maximum inhibition efficiency reaching 97.26% and 94.83% at 2.0 g/L MIPE concentration and solution temperatures of 303 K and 323 K, respectively. The uninhibited mild steel experienced increased corrosion rates with rising temperatures and longer immersion times. The inhibition efficiency of MIPE improved with higher extract concentrations and immersion periods. These findings underscore the potential of MIPE as an effective and environmentally friendly corrosion inhibitor in acidic environments.

Batch and column studies for the removal of basic red-46 dye and textile by using magnesium oxide (MgO), strontium titanium trioxide (SrTiO3), cobalt- and iron-doped lanthanum chromium trioxide (Co.Fe.LaCrO3), and cadmium sulfide (CdS)-doped graphene oxide nanocomposites.

Despite efforts to reduce the risk of toxic chemicals, colors, and dyes being released into the environment from urban and industrial areas, there is still cause for concern. Colored water must be filtered and sterilized before it can be used for irrigation. The utilization of metal oxide and nanocomposite materials in wastewater treatment procedures appears to be a viable option for the future. Therefore, different compounds were doped with graphene oxide to identify the best material for dye removal by the adsorption process. According to recent studies, the ideal conditions for graphene oxide-doped magnesium oxide (GO/MgO) are as follows: pH 10 showed the highest adsorption capacity (qe) at 49.4mg/g; an adsorbent dosage of 0.01g/50mL showed 48.3mg/g qe; a shaking time of 30min resulted in 44.2mg/g qe; an initial dye concentration of 100mg/L yielded 53.6mg/g qe; and a temperature of 35°C gave 49.5mg/g qe. For graphene oxide-doped strontium titanate (GO/SrTiO3), the optimum conditions were as follows: pH 10 with 45.8mg/g qe; an adsorbent dose of 0.01g/50mL with 40.5mg/g qe; a shaking time of 30min with 75mg/g qe; and a temperature of 35°C with 44.7mg/g qe. Graphene oxide-doped cobalt and iron-doped lanthanum chromium titanate (GO/Co.Fe.LaCrO3) showed optimum conditions of pH 9 with 34.2mg/g qe; an adsorbent dose of 0.01g/50mL with 27.5mg/g qe; a shaking time of 45min with 33.2mg/g qe; an initial dye concentration of 100mg/L with 37.6mg/g qe; and a temperature of 35°C with 42.5mg/g qe. Graphene oxide-doped cadmium sulfide (GO/CdS) showed the following optimum conditions: pH 8 with 23.1mg/g qe; an adsorbent dose of 0.01g/50mL with 25.5mg/g qe; an initial dye concentration of 75mg/L with 28.3mg/g qe; and a temperature of 35°C with 33.5mg/g qe. The pseudo-first-order model was the best fit only for graphene oxide-doped magnesium oxide (GO/MgO) with an R2 value of 0.966, while the pseudo-second-order adsorption isotherm was the best fit for all four products, with R2 values ranging from 0.991 to 0.998. Additionally, the Langmuir adsorption isotherms provided good results for all four products, with R2 values ranging from 0.957 to 0.985. The Freundlich adsorption kinetics showed satisfactory fit only for graphene oxide-doped magnesium oxide (GO/MgO) and graphene oxide-doped cadmium sulfide (GO/CdS), with R2 values of 0.951 and 0.982, respectively. To examine the characteristics and practicality of the adsorption process, certain thermodynamic variables were calculated. The adsorption capability of the most efficient nanocomposites for the degradation of basic red-46 was significantly affected by various concentrations of heavy metal ions and electrolytes. In dye solutions containing surfactants/detergents, the adsorption efficiency of several effective photocatalysts for basic dyes was significantly reduced. A 0.5M HCl solution was found to be the most effective for desorption. In column investigations, the optimal bed height, flow velocity, and dye intake levels were determined to be 3cm, 1.8mL/min, and 70mg/L, respectively, for maximal adsorption of basic red-46. The adsorption investigation of genuine textile waste products has also been carried out to facilitate the practical deployment of this approach. The methods used in this study were cost-effective, easy to handle, and eco-friendly and involved no hazardous materials in the synthesis, making the resulting materials non-hazardous. All these methods were part of green chemistry.

Exploring the Effectiveness of 3-Chloro-4-morpholin-4-yl-1,2,5-thiadiazole as a Eco-Friendly Corrosion Inhibitor for Mild Steel in HCl Solution: Experimental and DFT Analysis

Corrosion is a significant issue in many industries, particularly where metals are exposed to harsh chemical environments. This study investigates the efficacy of 3-Chloro-4-morpholin-4-yl-1,2,5-thiadiazole (CMTD) as a corrosion inhibitor for mild steel in 1 M HCl solution across a temperature range of 303–333 K. Using weight loss measurements, electrochemical impedance spectroscopy (EIS), and potentiodynamic polarization techniques, the inhibition efficiency of CMTD was evaluated at different concentrations and temperatures. The results show that CMTD achieves a maximum inhibition efficiency of 96.8% at a highest inhibitor concentration, even at elevated temperatures. The adsorption of CMTD on the mild steel surface follows the Langmuir adsorption isotherm, with a calculated free energy of adsorption (ΔGads) of -39.5 kJ/mol, confirming a spontaneous chemisorption process. Quantum chemical Density Functional Theory (DFT) studies further elucidated the relationship between CMTD's molecular structure and its inhibition efficiency. Key parameters, including the energy gap (Egap = 3.551 eV), highest occupied molecular orbital (EHOMO = -6.317 eV), and lowest unoccupied molecular orbital (ELUMO = -2.766eV), were calculated to understand CMTD's reactivity. Additionally, global reactivity descriptors such as chemical hardness (η), electronegativity (χ), and the electron fraction transferred (ΔN) from CMTD to the iron surface were analyzed. These findings suggest that CMTD is highly effective in preventing corrosion and can be applied in industries where mild steel is exposed to acidic environments, such as in petrochemical and industrial cleaning processes.

A multianalytical approach to benzodiazepine derivatives for the corrosion protection of mild steel in HCl solutions: Electrochemical analysis, SEM/EDX, XPS, DFT, and MDS calculations

A multianalytical approach to benzodiazepine derivatives for the corrosion protection of mild steel in HCl solutions: Electrochemical analysis, SEM/EDX, XPS, DFT, and MDS calculations