Kinetic Study Of Degradation Research Articles

Elimination of malachite green by modified Fenton like process. Application of Box Behnken design

<p style="line-height:200%;text-align:justify;"><span style="line-height:200%;" lang="EN-US">The aim of this work was to investigate an advanced oxidation process for removing malachite green from aqueous solutions using a modified Fenton-like process. An experimental Box-Behnken design was applied to determine the optimal conditions by examining the effects of catalyst concentration ([Fe<sup>2+</sup>]), oxidant concentration ([K<sub>2</sub>S<sub>2</sub>O<sub>8</sub>]), and stirring speed. The analysis of variance (ANOVA) indicated that oxidant concentration was the most significant factor, with a p-value of 0.001, while catalyst concentration, the quadratic term of the oxidant, and the interaction between catalyst concentration and stirring speed were also significant. The optimal conditions for maximum dye removal were found to be a catalyst concentration of 3.5 ppm, an oxidant concentration of 3.07 ppm, and a stirring speed of 200 rpm, achieving a theoretical degradation yield of 100% and an experimental yield of 98%. This agreement validates the model and the importance of the optimized parameters. Additionally, degradation kinetics studies in various natural waters revealed that oxidation efficiency followed this order: Distilled water (98%) > Seawater ≈ Industrial water (88.97%) > Source water (85.57%) > Mineral water (80.52%).</span></p>

Assessment of Blast Furnace Slags as a Potential Catalyst in Ozonation to Degrade Bezafibrate: Degradation Study and Kinetic Study via Non-Parametric Modeling

This study investigates the effectiveness of blast furnace slags (BFSs) as catalysts in the ozonation process to degrade complex contaminants such as bezafibrate (BFZ) at different pH levels. The findings reveal that the presence of BFS enhances degradation efficiency, achieving a 10% improvement at pH 10 and a 30% improvement at pH 5.5 compared to simple ozonation. The highest degradation efficiency was observed in the Ozonation–BFS system at pH 10, with 90% decomposition of BFZ. These results were corroborated through ozone consumption analysis, BOD5 measurements, and the identification of oxalic acid as the final decomposition product. Due to the complexity of the reaction system, kinetic characterization was performed using non-parametric modeling based on differential neural networks. The model indicated that the observed reaction rate for BFZ degradation in the presence of ozone and BFS was 4.12 times higher at pH 5.0 and 1.08 times higher at pH 10.0 compared to simple ozonation. These results underscore the potential of using BFS in catalytic ozonation processes for the effective treatment of recalcitrant contaminants in wastewater.

Kinetics Study of Carbaryl Degradation in Squash and Cucumber Fruits

Kinetics Study of Carbaryl Degradation in Squash and Cucumber Fruits

Facile synthesis of SrO/CeO2/alginate nanocomposite for the photocatalytic degradation of reactive red 195 dye and CO2 capturing

The SrO/CeO2/ALG nanocomposite was successfully constructed by using the co-precipitation method and was analyzed with zeta potential, FTIR, SEM, XRD and BET techniques. A common Azo dye, namely Reactive Red 195, widely utilized in the dyeing industry and causing environmental pollution, was chosen to examine the photodegradation of SrO/CeO2/ALG nanocomposite, and it was shown that this dye could be successfully degraded by prepared nanocomposite. Impacts of factors such as pH, contact time and effect of different concentrations of dye and catalyst, the effect of scavengers and the effect of hydrogen peroxide were investigated to find out degradation efficiency. This SrO/CeO2/ALG nanocomposite was used for the photodegradation of reactive red 195 dye and 93 % degradation efficiency was obtained at pH 3, 6 mg of catalyst concentration, dye concentration of 10 ppm, and contact time of 90 min. Degradation kinetic studies were determined by applying first-order and Langmuir-Hinshelwood reactions. The results exhibit a novel method for the synthesis of nanocomposite to effectively cause photodegradation of organic pollutants from wastewater and can be applied to industrial manufacture. The mesoporous SrO/CeO2/ALG nanocomposite also captured 4.31 and 2.98 mmol/g CO2 at 25 and 40 °C temperatures, respectively.

Thermal stability, preformulation, and kinetic degradation studies for gestrinone

AbstractGestrinone is an active pharmaceutical ingredient used in the treatment of endometriosis as capsules, with ongoing evaluation for intravaginal administration, while also having been studied for its potential antitumoral effects. The purpose of this study was to determine the compatibility of gestrinone with four excipients used in the development of solid pharmaceutical formulations (α-lactose monohydrate, magnesium stearate, starch, and talc) and to obtain a fully characterized thermoanalytical profile of gestrinone with the help of kinetic analysis. Preformulation studies were carried out on 1:1 mass/mass binary mixtures between gestrinone and each excipient by instrumental screening under ambient conditions using ATR-FTIR spectroscopy investigations, and later by studying the effect of thermal treatment over the samples (TG/DTG/DSC). The obtained results suggest that under ambient conditions, no chemical interactions take place between the active pharmaceutical ingredient and selected excipients, whereas under thermal stress incompatibilities are observed in all systems. The mechanism of decomposition was preliminary evaluated by the ASTM E698 and later completed by the isoconversional methods of Friedman, Kissinger–Akahira–Sunose, and Flynn–Wall–Ozawa, which suggest similar mean activation energies. The mechanism of decomposition was elucidated in the last part of the study, by employing the modified NPK method. This method suggests that gestrinone is thermally degraded by the contribution of two individual processes, both consisting of superimposed physical transformations and chemical degradations.

Innovative eco-friendly stability-indicating HPLC-PDA method for simultaneous determination of the emerging antiviral drugs against COVID-19 infection molnupiravir and favipiravir; degradation kinetic studies along with LC-MS based structure elucidation

The adoption of the principles of green chemistry in analytical procedures lowers the negative influence on both people and the environment, which presently has become the key goal. Additionally, the need for advanced analytical techniques for the simultaneous determination of antiviral combinations is highly recommended, one of those novel combinations that recently proved effective emerging antiviral drugs in the treatment of SARS-COV-2 is molnupiravir (MOL) and favipiravir (FAV). Therefore, the establishment of simple and precise stability-indicating HPLC-PDA method for their simultaneous determination is crucial for the probable co-formulation. The stability of MOL was studied along with FAV after forced degradation of both under different stress conditions Separation of MOL, FAV, and their corresponding degradation products was achieved by simple isocratic HPLC-PDA method using a mobile phase comprised of 25.0 mM phosphate buffer (pH 3.0 ± 0.05) − methanol (70:30, v/v) at flow rate 1.0 mL/min. A Zorbax C18 (250 × 4.6 mm, 5 μm; Agilent Technologies, USA) column was used for the separation of the components and the column oven was maintained at 30 °C, the selected wavelength for detection of both analytes and their degradation products was 230.0 nm. The method was linear over the range of 1.0 – 200.0 µg/mL for both MOL and FAV. MOL was found to be susceptible to all forced degradation conditions, namely, acid, alkali, oxidative, thermal, and photodegradation while FAV was susceptible only to acid, alkali, and oxidative degradation. The probable degradation mechanisms were assumed through the evaluation of the MS1 fragmentation pattern of the degradation products, also studying the kinetic behavior of the degradation reactions. Furthermore, the greenness profile for the proposed method was evaluated utilizing the new Complementary Green Analytical Procedure Index method (ComplexGAPI), and analytical greenness (AGREE) metrics with a score of the later one equals to 0.61 that indicated the greenness evaluation of the method. In addition, the new blue applicability grade index (BAGI) which is complementary to the green metrics showed a score of 85.0 that presents a good applicability potential of the method. The proposed method is the first sustainable, stability-indicating method developed for the simultaneous determination of this potential combination that would help in manufacturing both drugs in a fixed-dose drug combination.

Electrocatalytic coupled biofilter for treating cyclohexanone-containing wastewater: Degradation, mechanism and optimization

Electrocatalytic coupled biofilter (EBF) technology organically integrates the characteristics of electrochemistry and microbial redox, providing ideas for effectively improving biological treatment performance. In this study, an EBF system was developed for enhanced degradation of cyclohexanone in contaminated water. Experimental results show that the system can effectively remove cyclohexanone in contaminated water. Under the optimal parameters, the removal rates of cyclohexanone, TP, NH4+-N and TN were 97.61 ± 1.31%, 76.31 ± 1.67%, 94.14 ± 2.13% and 95.87 ± 1.01% respectively. Degradation kinetics studies found that electrolysis, adsorption, and biodegradation pathways play a major role in the degradation of cyclohexanone. Microbial community analysis indicates that voltage can affect the structure of the microbial community, with the dominant genera shifting from Acidovorax (0 V) to Brevundimonas (0.7 V). Additionally, Acidovorax, Cupriavidus, Ralstonia, and Hydrogenophaga have high abundance in the biofilm and can effectively metabolize cyclohexanone and its intermediates, facilitating the removal of cyclohexanone. In summary, this research can guide the development and construction of highly stable EBF systems and is expected to be used for advanced treatment of industrial wastewater containing cyclohexanone.

Highly efficient adsorption assisted photocatalytic decontamination of metronidazole by Co3O4 doped graphitic carbon nitrides

Since traditional wastewater treatment techniques only partially remove antibiotics like metronidazole (MTZ), the rising use of these drugs causes their entry into wastewater and receiving surface waterways. A flexible method that may effectively degrade such organic pollutants is adsorption assisted photocatalytic degradation. Herein, an easy mixing-and-heating procedure was used to synthesize visible light-induced g-C3N4/Co3O4 heterojunction photocatalysts. The structural properties and morphology of as-prepared materials were measured using characterization techniques such as FTIR, FSEM, and XRD analysis. The as-prepared catalyst has demonstrated a remarkable adoption and photocatalytic performance in degrading MTZ. It was found that 0.2 weight percent of Co3O4 was the optimum amount for achieving the best photocatalytic efficiency. A key factor in boosting photo-generated carrier separation is the synergistic interaction between g-C3N4 and Co3O4. The kinetics study of MTZ adsorption and degradation as well as factors effecting such as pH (2-10) and catalyst dosage process were investigated. The functional treatment method attained 78% degradation of MTZ under the following general conditions: pH = 6, g-C3N4/Co3O4 = 0.04 g/L, and reaction time = 200 min and MTZ concentration = 20 mg/L. A possible mechanism for the photocatalytic degradation was introduced, wherein O 2 • − was found to be the leading radical, whereas h + and H O • radicals contribute moderately to the degradation process. The research presents an appealing and environmentally friendly technique for the practical remediation of waste water carrying antibiotics.

Green Synthesis, Characterization, and Evaluation of Photocatalytic and Antibacterial Activities of Co3O4-ZnO Nanocomposites Using Calpurnia aurea Leaf Extract.

The green synthesis of transition metal oxide nanocomposites using plant extracts is a new and effective method that avoids the involvement of hazardous chemicals. Nondegradable organic pollutants and antibiotic drug resistance have become serious public health issues worldwide. Hence, the main objective of this study is to synthesize Co3O4-ZnO nanocomposites using Calpurnia aurea leaf extract and evaluate its photocatalytic and antibacterial activities. The green synthesized particles were characterized using UV-vis spectra, Fourier transform infrared spectroscopy, X-ray diffraction techniques, and scanning electron microscopy combined with energy-dispersive X-ray studies. The synthesized particles were found to be crystalline in nature with average crystallite sizes of 23.82, 14.79, 15.99, 16.46, and 21.73 nm. Scanning electron microscopy shows the spherical morphology of Co3O4-ZnO NCs, and energy-dispersive X-ray analysis confirms the formation of highly pure ZnO NPs and Co3O4-ZnO NCs. The photocatalytic activity was performed under natural sunlight using malachite green as an organic dye pollutant. The green synthesized ZnO NPs, Co3O4 NPs, 1:4, 1:3, and 1:2 Co3O4-ZnO NCs showed high degradation efficiency after 60 min of irradiation. The synthetic material showed good potential against Staphylococcus aureus and Escherichia coli, with the highest growth inhibition recorded by 1:2 Co3O4-ZnO NCs. The kinetics study of the photocatalytic degradation was confirmed as pseudo first order, and the possible mechanisms for both photocatalytic and antibacterial activities were clearly determined.

Study of Oxidative Degradation and Mineralization Kinetics and Oxidation Products of Ofloxacin in Water via Electro-Fenton Method with Pt Anode, and Biodegradation Optimization

Study of Oxidative Degradation and Mineralization Kinetics and Oxidation Products of Ofloxacin in Water via Electro-Fenton Method with Pt Anode, and Biodegradation Optimization

Accelerated Photocatalytic Degradation of Sulfamethoxazole and Cefixime: A Comprehensive Study of Biotoxicity, Degradation Kinetics and Pathway

Accelerated Photocatalytic Degradation of Sulfamethoxazole and Cefixime: A Comprehensive Study of Biotoxicity, Degradation Kinetics and Pathway

Effect of metals and brominated flame retardants on thermal degradation kinetics of waste printed circuit board

Waste printed circuit board (WPCB) is an indispensable component in any waste electrical and electronic equipment (WEEE). A promising method for recycling WPCB is pyrolysis. To understand the effect of metals and brominated flame retardants (BFR) on WPCB pyrolysis, four samples were prepared, namely (a) raw WPCB (RW), (b) non-metallic WPCB (NM), (c) bromine extracted WPCB (RWBFR_ext) and (d) bromine and metal extracted WPCB (NMBFR_ext). The degradation kinetics study using the isoconversional methods: Friedman, Ozawa-Flynn-Wall (OFW), Kissinger–Akahira–Sunose (KAS), and Starink showed that the extraction of metals exhibited an increase in final degradation temperature and activation energy (Eα), and altered the reaction mechanism (f(a)) whereas, the reduction of BFR reduced initial degradation temperature. The identified kinetic triplets were verified using the reconstruction profiles. The parameters can be used in designing applications and developing an energy-efficient pyrolysis process.

Development of a stability indicating high-performance liquid chromatography method for determination of cenobamate: study of basic degradation kinetics

This study presents a stability indicating high-performance liquid chromatography HPLC method for the determination of cenobamate (CNB) in presence of its main impurity (CNB H-impurity) and degradation products. The chromatographic separation was carried out on a Thermo BDS Hypersil-C18 column (150 × 4.6 mm; 5 μm) with a mobile phase consisting of a 50:50 (%v/v) ratio of methanol and purified water. The flow rate was maintained at 1.0 mL. min− 1. CNB was detected at 210 nm using a PDA detector. The column temperature was held at 40 °C.The retention time of the drug was found to be 3.2 min. Furthermore, the study investigates the degradation behavior of CNB under various stress conditions, including acidic, basic, oxidative, and light-induced degradation. The results indicate that CNB is particularly susceptible to basic degradation. Consequently, a comprehensive study of the basic degradation kinetics was conducted. The method was also successfully applied for the determination of CNB in its dosage form. The results also show that there is no co-elution from degradation products or excipients as indicated by the mass balance and peak purity values confirming the specificity of the proposed method and its applicability for routine analysis of CNB.

Study of Structural Elucidation, Degradation Kinetics and Antimicrobial Analysis of Copper (II) Sesame-Soap Complexes with Urea and Thiourea Ligand in Non-aqueous Solvents

Abstract: Surfactants have great importance in biological and drug industries and the complexes of metallic soaps with various ligands are used in approximately every region of national economy. Therefore, our keen interest to study of degradation kinetics and biological importance of Cu (II) surfactants in non-aqueous and non-polar solvent benzene. Present research work has been initiated with synthesis, systematic study of structural elucidation, thermal degradation, kinetics and biocidal activities of copper (II) sesame-soap complexes with macrocyclic nitrogen and sulphur containing donar ligands like urea and thiourea. The thermal degradation of copper (II) sesame-soap complexes were carried out for analysis of degradation kinetics and estimation of kinetic and thermodynamic parameters using different methods at heating rate 10oC min-1. Copper (II) sesame-soap complexes of such ligands have also been analysed against Staphylococus aureus. This research work consolidates the synthesis of copper (II) sesame soap-urea and thiourea complexes by conventional methods and the structure of these complexes were assigned according to elemental analysis and molecular weight determinations. IR, NMR and ESR spectral studies have also been done to understand structural aspects. The anti-microbial activities of copper (II) sesame-soap urea and thiourea complexes have been evaluated by testing against Staphylococus aureus. The present research work includes information of thermal analysis using TGA technique to find out their kinetic and thermodynamic parameters by using diverse equations such as Coats-Redfern equation, Horowitz-Metzger equation, Broido equation, Piloyan–Novikova equation. Moreover, the results obtained from anti-microbial screening have been used to analyze the anti-microbial activities of copper (II) sesame-soap urea and thiourea complexes against gram-positive bacteria Staphylococus aureus. These results show that complexes of copper ion co-ordinated with different nitrogen, oxygen and sulphur containing ligands, are very important in the field of pharmaceutical chemistry due to its significant role in the inhibition activity. The study of these complexes concludes that the synthesized complexes were found to possess appreciable bactericidal properties at different concentrations because chelation increases the anti-microbial potency.

Kinetic Study of Sodium Dodecylsulfate Degradation by Solar Heterogeneous Photocatalysis Based on Tungsten Oxide

Sodium Dodecyl Sulfate or SDS is a chemical compound widely used in detergent and cosmetic formulations. This work describes the application of solar heterogeneous photocatalysis based on tungsten oxide (WO3) to the kinetic study of the degradation of sodium dodecylsulfate. The experiments were performed at room temperature to study the effect of the initial catalyst mass. The results showed that a small amount of tungsten oxide is sufficient to degrade sodium dodecyl sulfate. The initial concentrations of SDS varied between 5 and 15 mg.L-1. According to the results, more than 87% reduction is obtained after 120 min of solar irradiation of the SDS solution for a WO3/SDS mass ratio of 1/5. The detailed kinetic analysis of the photodegradation of sodium dodecylsulfate showed that the disappearance of the anionic surfactant follows a pseudo-prime model. According to the Langmuir-Hinshelwood model, the kinetics constant calculated from the linear form of this model are : k = 0.042 mg.L.min-1 and K = 0.060 L.mg-1.

Adsorption of stable and labile emerging pollutants on activated carbon: degradation and mass transfer kinetic study

The design of adsorption processes for pharmaceuticals removal depends not only on the adsorption equilibrium but also on the mass transfer and adsorbate stability, being a problem still not solved the case of degradation products. By selecting different stable (amoxicillin, ciprofloxacin, carbamazepine and ibuprofen) and labile micropollutants (omeprazole) as case studies emerging pollutants, we have quantitatively analysed these effects on activated carbon. For stable compounds, the experimental data were fitted to equilibrium models to obtain information about the different adsorption mechanism depending on the characteristics of the molecules. Mass transfer effects were analysed for all the adsorbates, observing the control of intraparticle pore diffusion mechanism, since the effective pore diffusion coefficient is in the range from 10–8 to 10–10 cm2 h−1. As far as omeprazole is concerned, a kinetic model is proposed for predicting its degradation, identifying the reversibility of several degradation steps. The overall adsorption of OMP and derivates is calculated, observing the pore diffusion is considered as the rate-limiting step. For the first time, a combined model considering the chemical degradation and the adsorption of the degradation products is proposed and experimentally validated. This represents an important step in the modelling of processes leading to the purification of water from this type of pollutant.

The Study of Photocatalytic Degradation Kinetics and Mechanism of Malachite Green Dye on Ni–TiO2 Surface Modified with Polyaniline

Synthetic organic dyes are coloring agents used in various industries. Despite the fact that they offer exciting colors and long-lasting effects, certain organic dyes can have harmful impacts on human health and aquatic ecosystems. This study investigates the photocatalytic degradation of malachite green dye using Ni–TiO2 nanoparticles (NPs) and Ni–TiO2/PANI nanocomposites (NCs) in various reaction conditions. The surface and compositional change of synthesized photocatalysts were characterized by XRD, FTIR, AAS, and UV–vis spectrophotometer. Accordingly, the XRD results signify the crystal structure of photocatalysts found to be tetragonal anatase phase while the FT-IR spectra indicate the titanium has predominantly form a coordination compound upon reaction with nitrogen atom through weakening the bond strength between C═N, C═C, and C─N in the PANI. The UV–vis measurement shows that the energy bandgaps were decreased from 3.20 to 2.77 eV and 2.59 eV for Ni–TiO2 NPs and Ni–TiO2/PANI NCs, respectively. From AAS data, the authors confirmed that Ni metal has significantly existed in the aforementioned photocatalysts after the calcination process. The photocatalytic degradation of Ni–TiO2 NPs and Ni–TiO2/PANI NCs on the model dye has studied and their efficiency was 94.22% and 99.09%, respectively. The photocatalytic degradation follows pseudo-first order with 2.23 × 10−2 min−1 reaction rate at optimum conditions of pH 8.5, initial dye concentration of 0.2 g/L, catalyst load of 0.2 g/L, and irradiation time of 90 min. With this, the outstanding result recorded using Ni–TiO2/PANI NCs is ascribed to the smaller particle size as compared to Ni–TiO2 NPs, and it is found to be the promising photocatalyst for the removal of wastewater containing organic dyes.

Valorization of cashew nut testa phenolics through nano-complexes stabilized with whey protein isolate and β-cyclodextrin: Characterization, anti-oxidant activity, stability and in vitro release

Cashew nut testa (CNT) is an underutilized cashew by-product rich in polyphenols. The applications of CNT are limited due to its astringency, less solubility, and instability of polyphenols during the processing. Nanoencapsulation was used to overcome these limitations. β-cyclodextrin alone and in combination with whey protein isolate (WPI) was used for nano-complex preparation. The WPI/CD-CNT nano-complex powder showed higher encapsulation efficiency (86.9%) and yield (70.5–80%) compared to CD-CNT powder. Both the spray-dried powders showed improved thermal stability, higher solubility (97%), less moisture content, and increased DPPH and ABTS radical scavenging activities indicating potential food and agricultural applications. In addition, the nano-complex powders showed a controlled release of core bio-actives under gastric and intestinal pH compared to the non-encapsulated CNT phenolic extract. Degradation kinetics studies of the CNT extract after thermal and light treatments were also discussed. Both the nano-complexes showed high stability under light and thermal treatment. The results suggest that valorization of CNT can be done through nano-complex preparation and WPI and β-CD are efficient carrier materials for the encapsulation of polyphenols with potential applications in food and agriculture.

Visible-light-driven photodegradation of methylene blue and doxycycline hydrochloride by waste-based S-scheme heterojunction photocatalyst Bi5O7I/PCN/tea waste biochar

Herein, we have reported a photocatalytic Bi5O7I, protonated g-C3N4 heterojunction with directional charge transfer channels provided by tea waste biochar to achieve effective e−/h+ pair isolation for the improved degradation of Methylene blue (MB) and Doxycycline hydrochloride (DCHCl). An S-scheme heterojunction was fabricated via the novel method that combined hydrothermal and ultrasonic dispersion, followed by an electrostatic self-assembly route. The as-fabricated Bi5O7I/protonated g-C3N4/Tea waste biochar heterojunction formed a strong contact at the interface, as supported by the electron microscopic results. As per the adsorption and photocatalytic degradation kinetics study, Bi5O7I/Tea waste biochar/protonated g-C3N4 (40 wt%) heterojunction showed a higher adsorption rate of 41.56% and 32% for MB and DCHCl within 30 min in the dark. Also, 92.02% MB and 90.21% DCHCl degradation rates in 60 and 90 min, respectively, are approximately 43 and 32 times higher than bare Bi5O7I and protonated g-C3N4 photocatalysts. The highest adsorption and degradation rate was achieved owing to the addition of Tea waste biochar and protonated g-C3N4 in a controlled ratio, and the sufficient interfacial contact between Bi5O7I and protonated g-C3N4 is for the improved isolation rate of e−/h+ pairs as evidenced by zeta potential values photoluminescence spectra as well as from scanning and transmission electron microscopy. Moreover, Bi5O7I/Tea waste biochar/protonated g-C3N4 (40 wt%) possessed high stability and recyclability after four consecutive cycles without much altering the degradation ability. Therefore, we believe that the as-fabricated Bi5O7I/Tea waste biochar/protonated g-C3N4 (40 wt%) provides new insight into the highly efficient S-scheme mechanisms significant for accelerating multicomponent photocatalytic redox reactions; while forming an effective visible light responsive candidate for treating wastewater.

Protective and water-repellent properties of alkylcarboxylic and alkylphosphonic acid films on technically pure magnesium

The formation of superhydrophobic coatings using low‑toxicity corrosion inhibitors is a promising method for corrosion protection of metals and alloys. In this study, the effects of surface roughness and the of the adsorbed substance structure on wettability and corrosion resistance of commercially pure magnesium were investigated. Surface roughness was created by three different methods: paper grinding, etching in nitric acid solution and laser treatment. Oleic, stearic and octadecylphosphonic acids were investigated as potential surface modifiers for the formation of corrosion resistant superhydrophobic coatings. It has been shown that the protective and hydrophobic properties of acid films on magnesium, as well as their stability, are determined by both the initial surface morphology and the nature of the inhibitors. Experimentally, the laser treatment was found to be preferable to mechanical and chemical surface preparation and the best hydrophobic agent among the studied acids is phosphonic acid. The most stable films with excellent superhydrophobic and protective properties in atmospheres of high humidity and salt spray clamber are formed in a solution of 0.001 M octadecylphosphonic acid on the surface of magnesium with high roughness. In addition, the effect of vinyltrimethoxysilane on the protective and hydrophobic properties of stearic acid and octadecylphosphonic acid films was investigated. The results of direct corrosion tests and wetting contact angle degradation kinetics studies showed that the protective and hydrophobic properties of stearic acid can be enhanced by its layer-by-layer adsorption with silane. They practically reach the parameters of octadecylphosphonic acid.