Solutions Of Carboxylic Acids Research Articles

Unravelling competitive adsorption phenomena in the aqueous phase reforming of carboxylic acids on Pt catalysts: An experimental and theoretical study

Biorefinery-derived wastewater is considered a valuable source of energy and chemicals thanks to its organic loading. However, it is constituted by different compounds which influence the performance of a catalytic valorization process. In this work, we investigated the treatment of a synthetic hydrothermal liquefaction-derived wastewater (HTL-WW) via aqueous phase reforming (APR) to obtain hydrogen. As a case study, we examined the underlying driving forces for performance differences in the APR of mono- and bi-component solutions of carboxylic acids as a model corn stover HTL-WW over Pt catalysts via a combined experimental and theoretical approach. In mono-component solutions, the conversion ranked as glycolic acid > propionic acid ≈ acetic acid, and the same was found for the hydrogen production tendency. Binary solutions of glycolic and acetic acid, with different concentration among the constituents, showed a strong inhibition of the acetic acid reactivity due to the prevalent adsorption of glycolic acid on Pt surface. The results from the APR of acetic and propionic acid solutions were less affected by such phenomena. DFT results showed that there are strong, attractive lateral interactions between carboxylic acids due to intermolecular hydrogen bonding that cause all carboxylic acids to preferentially adsorb in dimer structures. The lateral interaction strength was determined for both pure and binary mixtures of carboxylic acid dimers, with results showing that pure mixtures of carboxylic acids have stronger attractions and that glycolic acid dimers see the strongest attractions due to the added terminal hydroxyl functional group. The findings presented herein offer significant insights into the utilization of APR for industrial-like multi-component solutions, as well as for any catalytic process involving small organic compounds in an aqueous phase.

Green extraction of berberine from Coscinium fenestratum (Gaertn.) Colebr. using ultrasound-assisted aqueous solutions of organic acids, polyalcohols, and deep eutectic solvents

Berberine displays many potential bioactivities and is found in several medicinal herbs, such as Coscinium fenestratum. The extraction of berberine from biomass was carried out using volatile organic solvents, inorganic acid solutions, and more recently, ionic liquids and deep eutectic solvents. In order to develop more efficient and sustainable extraction processes, this study used inexpensive green solvents, such as carboxylic acid and polyalcohol aqueous solutions, to extract berberine from Coscinium fenestratum. Initial screening was performed to compare the berberine extraction performance of various solvents, including aqueous solutions of carboxylic acids, polyalcohols, and their deep eutectic solvents. The obtained results showed that lactic acid was a potential solvent for extracting berberine. After optimizing the process using response surface methodology (RSM), the optimal ultrasound-assisted extraction conditions were determined to be a lactic acid concentration of 60 % (w/w), a liquid-to-solid ratio of 17.25 mL/g, an extraction time of 20 min, and an extraction temperature of 66 °C. This resulted in an extraction efficiency of 38.23 ± 0.69 mg/g, corresponding to a berberine concentration of 2.22 ± 0.04 mg/mL. Additionally, the use of lactic acid as the extraction solvent yielded superior extraction efficiency and berberine purity compared to conventional volatile organic solvents, and inorganic acids, bases. The recovery of berberine was achieved using macroporous resins, allowing for the recovery of 99.52 ± 0.67 % of berberine from aqueous lactic acid solutions. The lactic acid solvent and the AB-8 resin were successfully recovered and reused for a minimum of three consecutive extraction cycles, maintaining their full effectiveness throughout the entire process. The recovered berberine from the lactic acid extract exhibited stronger antibacterial activity than the extracts obtained using ethanol, methanol, and acetone, as well as berberine recovered from the limewater and sulfuric acid extracts. Furthermore, the lactic acid solvent and its extracts demonstrated no cytotoxicity toward the human embryonic kidney cell line. The findings of this investigation establish a foundation for future studies utilizing eco-friendly solvents for alkaloid extraction from medicinal plants. This lays the groundwork for implementing a large-scale extraction process of natural active compounds in a safe and environmentally conscious manner.

Sub-ppm determination of perfluorinated carboxylic acids in solution by UV–vis high-performance liquid chromatography through solid phase extraction

This study investigated a novel and sensitive analytical method based on a simple heat-based derivatization using 3-bromoacetyl coumarin as the reagent and analysis with a HPLC-UV system or just a UV–vis spectrometer to allow the sub-ppm determination of PFCAs in water solution with the potential for utilization in simple laboratories and field laboratory scenarios. A Strata-X-AW cartridge was used for the solid phase extraction (SPE) procedure and higher than 98% recoveries were obtained. The derivatization condition showed that a high efficiency of peak separation was obtained with obviously different retention time among various PFCAs derivatives using HPLC-UV analysis. The derivatization stability and repeatability showed favorable results with stable derivatized analytes for ≤12 h and a relative standard deviation (RSD) of <2% for all repetitions. The limit of detection for the HPLC-UV analysis was between 0.1 ppm and 0.5 ppm. A satisfactory linearity response was found with R 2 >0.998 for all individual PFCA compounds. The limit of detection for simple UV-Vis analysis was <0.0003 ppm to measure the presence of PFCAs. Contamination of standards with humic substances and measurement of industrial samples in a complex wastewater matrix showed no adverse effects on the accuracy of PFCA determination by using the developed methodology.

Early Microjet Experimentation with Liquid Water in Vacuum.

ConspectusIn this brief look at the history of liquid microjets, I recollect some personal reminiscences on initial challenges for introduction of this method, as well as unexpected problems and exemplary results using this new tool for liquid evaporation and photoelectron spectroscopy studies.Many efficient and direct, atomic level diagnostic instruments in use at solid state surfaces and in gas-phase atom or cluster studies require high vacuum. They have therefore not been applied to investigations of aqueous solutions because liquid water both strongly evaporates and rapidly freezes in vacuum. Only fairly recently, over the past three decades, have liquid microjets been considered as practicable targets for research on liquid-water interfaces in vacuum. The working principle is analogous to the functioning of a free molecular beam source, where molecules enter through a small aperture into a vacuum without being disturbed by subsequent collisions in their original Maxwellian velocity distribution. Similarly, above a microjet surface in vacuum, water vapor molecules do not interact with each other, or with different probe particles, as long as the liquid jet diameter is small in relation to the mean free path of the liquids' vapor at equilibrium conditions. For pure liquid water, this constraint is Djet < λvap < 10 μm for 6.1 mbar vapor pressure at the triple point of water. A high streaming velocity of the liquid jet, >50 m/s, delays freezing and exposes a steadily renewed fresh vacuum surface for experiments.For experimental verification of the microjet free surface concept, H2O vapor velocities were measured in a molecular beam time-of-flight experiment. These studies showed Maxwellian velocity distributions with the expected local water-jet temperatures for 5 and 10 μm jets, whereas larger liquid jet diameters of 50 μm exhibit narrowed vapor velocity profiles. This narrowing is the known signature of incipient, collision dominated, supersonic hydrodynamic expansions in nozzle beam sources. As a completely unexpected new result in evaporation studies of carboxylic acid solutions, freely evaporating acetic acid dimers showed apparent non-equilibrium liquid surface source temperatures several hundred kelvin above the simultaneously measured monomer temperatures, a phenomenon shown to be correlated with surface tension.Continuing with improvements, the vacuum water microjets were implemented inside a photoelectron spectroscopy apparatus that was modified for handling large amounts of water vapor. After initial complications with liquid jet charging phenomena, the first partial liquid-water photoelectron spectra were recorded using 21 eV photons from a He I discharge lamp. In the next step, the equipment was taken to a synchrotron radiation beamline at BESSY II, resulting in substantial improvements of signal intensity and in photon tunability for narrow band monochromatic soft X-rays up to 1 keV. Two early examples of these continuing experiments are considered, briefly, for aqueous alkali halide salt solutions and for the pH-value dependent protonation of an NH2/NH3+ group in an amino acid directly in a photoelectron spectrum of a solution.In conclusion, liquid microjets have opened up a completely new approach to studies of arbitrary liquids with chemical and biological relevance.

Контракция неводных растворов спиртов и кислот

Contraction is a non-additive change in the volume of a solution with a change in the concentration of one of its components. Contraction is caused by the formation of compounds based on mole-cules / ions of the solute and molecules of the solvent due to electrostatic interaction and the occur-rence of hydrogen or other bonds. This effect, inherent in all true solutions, is still rarely taken into account in the analysis of hydrodynamic and heat/mass transfer phenomena. The reason for this situation is the lack of information on contraction for most liquidsystems. To eliminate this draw-back, the presented study determines the contraction of non-aqueous solutions of mono-and polya-tomic alcohols and carboxylic acids. The obtained data are systematized and analyzed, a number of fluidsystems are proposed for laboratory modeling of diffusion processes in microgravity.

Corrosion Behavior of Aluminum in some Short-chain Carboxylic Acid solutions as a Simulant for Cooling Water in HVDC Transmission

Corrosion Behavior of Aluminum in some Short-chain Carboxylic Acid solutions as a Simulant for Cooling Water in HVDC Transmission

Modeling the Solvation and Acidity of Carboxylic Acids Using an Ab Initio Deep Neural Network Potential.

Formic and acetic acid constitute the simplest of carboxylic acids, yet they exhibit fascinating chemistry in the condensed phase such as proton transfer and dimerization. The go-to method of choice for modeling these rare events have been accurate but expensive ab initio molecular dynamics simulations. In this study, we present a deep neural network potential trained using accurate ab initio data that can be used in tandem with enhanced-sampling methods to perform an efficient exploration of the free-energy surface of aqueous solutions of weak carboxylic acids. In particular, we show that our model captures proton dissociation and provides a good estimate of the pKa, as well as the dimerization of formic and acetic acid. This provides a suitable starting point for applications in different research areas where computational efficiency coupled with the accuracy of ab initio methods is required.

Viscosity of Binary Aqueous Solutions Involving Malonic, Maleic, Malic, Tartaric, and Citric Acids in the Temperature Range between 303 and 363 K: Experimental Data and Modeling

Kinematic viscosity is a key property for the design of flow systems. This transport property is directly dependent on temperature and concentration and indirectly dependent on molecular interactions that take place in a mixture. Carboxylic acids are a class of chemical compounds with employment in a large variety of processes and applications. The viscosity of carboxylic acid solutions changes due to the acid size and its concentration. The application of models can provide property prediction and generate information about molecular interactions in a mixture. This work studies the kinematic viscosity of binary aqueous solutions of carboxylic acids (malonic, maleic, malic, tartaric, and citric acids) at different temperatures (from 303.2 to 363.2 K with an increment of 10 K) and concentrations (from 0.5 to 3.0 mol·kg–1 with an increment of 0.5 mol·kg–1). The data were treated by the Eyring equation combined with the UNIFAC model. The experimental results and thermodynamic properties indicate that the kinematic viscosity is strongly influenced by the size of carboxylic acid and the molar mass of the binary solution. The suggested modeling showed capability of correlating the experimental data.

Sensitization mechanism of metal oxide nanocluster resists with carboxylic acid ligands

Metal oxide nanocluster resists are a promising candidate for enabling the high-volume production of semiconductor devices with high-numerical-aperture extreme ultraviolet exposure tools. In this study, the sensitization mechanism of metal oxide nanocluster resists was investigated by focusing on the radiation-induced reactions of carboxylic acid ligands. Radiolytic products in various solutions of unsaturated carboxylic acids, aromatic carboxylic acids, and saturated carboxylic acids were analyzed by electrospray ionization mass spectrometry, high-performance liquid chromatography, and dynamic light scattering. The conditions of the solutions were selected to control reaction paths of intermediates. The major reaction paths induced by ionizing radiation were clarified. The obtained results suggest that the generation of bridging ligands is essential to the sensitization of metal oxide nanocluster resists. Both low-energy electrons and radical cations can trigger dimerization. The diffusion of small radicals should be suppressed to prevent dimerization at undesired places.

Cloud point, auto-coacervation, and nematic ordering of micelles formed by ethylene oxide containing carboxylate surfactants

HypothesisIn a recent paper, we determined the phase behavior of an aqueous solution of octyl ether octaethylene oxide carboxylic acid ([H+][C8E8c−], Akypo™ LF2) and with partial replacement of H+ by Na+ and Ca2+. It was found that even the neat surfactants are liquid at room temperature and that they form only direct micelles for any aqueous content and over large temperature ranges. The aim of the present work was to find an explanation for the clouding in these systems as well as for the coacervation observed at very low surfactant content. We expected that very similar phase diagrams would be found for a full replacement of H+ by the mentioned ions. ExperimentsWe established the respective phase diagrams of the above-mentioned salts in water and determined the structures of the occurring phases in detail with small-and wide-angle X-ray scattering, small-angle neutron scattering, dynamic light scattering, heat flux differential scanning calorimetry, as well as surface tension, ESI-MS, and NMR experiments. FindingsTo our surprise, we discovered a new type of nematic phase between an isotropic and a hexagonal phase. Based on the complete description of all occurring phases both in the acidic and the charged surfactant systems, we were able to design a coherent and unified picture of all these phases, including the auto-coacervation at low surfactant concentration, the non-conventional clouding at high temperatures, the unusual liquid crystalline phases in a small domain at high surfactant concentrations, and the Lβ phase at low temperatures and at very low water content. It turned out that all phenomena are a consequence of the subtle interplay between a) the packing constraint due to the very large head-group, b) the relatively small hydrocarbon chain and c) the tunable electrostatic interactions versus entropy.

Designing Carbon-Enriched Alumina Films Possessing Visible Light Absorption.

Aluminum anodization in an aqueous solution of formic acid and sodium vanadate leads to the formation of alumina/carbon composite films. This process was optimized by varying the concentrations of formic acid and sodium vanadate, the pH, and the processing time in constant-voltage (60–100 V) or constant-current mode. As estimated, in this electrolyte, the anodizing conditions played a critical role in forming thick, nanoporous anodic films with surprisingly high carbon content up to 17 at.%. The morphology and composition of these films were examined by scanning electron microscopy, ellipsometry, EDS mapping, and thermogravimetry coupled with mass spectrometry. For the analysis of incorporated carbon species, X-ray photoelectron and Auger spectroscopies were applied, indicating the presence of carbon in both the sp2 and the sp3 states. For these films, the Tauc plots derived from the experimental diffuse reflectance spectra revealed an unprecedentedly low bandgap (Eg) of 1.78 eV compared with the characteristic Eg values of alumina films formed in solutions of other carboxylic acids under conventional anodization conditions and visible-light absorption.

Recovery Techniques Enabling Circular Chemistry from Wastewater.

In an era where it becomes less and less accepted to just send waste to landfills and release wastewater into the environment without treatment, numerous initiatives are pursued to facilitate chemical production from waste. This includes microbial conversions of waste in digesters, and with this type of approach, a variety of chemicals can be produced. Typical for digestion systems is that the products are present only in (very) dilute amounts. For such productions to be technically and economically interesting to pursue, it is of key importance that effective product recovery strategies are being developed. In this review, we focus on the recovery of biologically produced carboxylic acids, including volatile fatty acids (VFAs), medium-chain carboxylic acids (MCCAs), long-chain dicarboxylic acids (LCDAs) being directly produced by microorganisms, and indirectly produced unsaturated short-chain acids (USCA), as well as polymers. Key recovery techniques for carboxylic acids in solution include liquid-liquid extraction, adsorption, and membrane separations. The route toward USCA is discussed, including their production by thermal treatment of intracellular polyhydroxyalkanoates (PHA) polymers and the downstream separations. Polymers included in this review are extracellular polymeric substances (EPS). Strategies for fractionation of the different fractions of EPS are discussed, aiming at the valorization of both polysaccharides and proteins. It is concluded that several separation strategies have the potential to further develop the wastewater valorization chains.

Absorption Spectra and the Electronic Structure of Gallic Acid in Water at Different pH: Experimental Data and Theoretical Cluster Models.

Gallic acid (GA) has been characterized in terms of its optical properties in aqueous solutions at varying pH in experiments and in theoretical calculations by analyzing the protonated and deprotonated forms of GA. This work is part of a series of studies of the optical properties of different carboxylic acids in aqueous media. The experimental electronic spectra of GA exhibit two strong well-separated absorption peaks (B- and C-bands), which agree with previous studies. However, in the current study, an additional well-defined low-energy shoulder band (A-band) in the optical spectra of GA was identified. It is likely that the A-band occurs for other carboxylic acids in solution, but because it can overlap with the B-band, it is difficult to discern. The theoretical calculations based on density functional theory were used to simulate the optical absorption spectra of GA in water at different pH to prove the existence of this newly found shoulder band and to describe and characterize the full experimental optical spectra of GA. Different cluster models were tested: (i) all water molecules are coordinated near the carboxy-group and (ii) additional water molecules near the hydroxy-groups of the phenyl ring were included. In this study, we found that both the polarizable continuum model (dielectric property of a medium) and neighboring water molecules (hydrogen-bonding) play significant roles in the optical spectrum. The results showed that only an extended cluster model with water molecules near carboxy- and hydroxy-groups together with the polarizable continuum model allowed us to fully reproduce the experimental data and capture all three absorption bands (A, B, and C). The oscillator strengths of the absorption bands were obtained from the experimental data and compared with theoretical results. Additionally, our work provides a detailed interpretation of the pH effects observed in the experimental absorption spectra.

Bulk Response of Carboxylic Acid Solutions Observed with Surface Sum-Frequency Generation Spectroscopy.

We study the molecular properties of aqueous acetic acid and formic acid solutions with heterodyne-detected vibrational sum-frequency generation spectroscopy (HD-VSFG). For acid concentrations up to ∼5 M, we observe a strong increase of the responses of the acid hydroxyl and carbonyl stretch vibrations with increasing acid concentration due to an increase of the surface coverage by the acid molecules. At acid concentrations >5 M we observe first a saturation of these responses and then a decrease. For pure carboxylic acids we even observe a change of sign of the Im[χ(2)] response of the carbonyl vibration. The decrease of the response of the hydroxyl vibration and the decrease and sign change of the response of the carbonyl vibration indicate the formation of cyclic dimers, which only show a quadrupolar bulk response in the HD-VSFG spectrum because of their antiparallel conformation. We also find evidence for the presence of a quadrupolar response of the CH vibrations of the acid molecules.

Modelling of chromatographic carboxylic acid fractionation with a strong anion exchange resin in sulfate form

Chromatographic fractionation of complex mixtures of carboxylic acids with a strong anion exchange resin in sulfate form as separation material was modelled. The studied system contained lactones of two isosaccharinic acids, four dissociating monocarboxylic acids (lactic acid, glycolic acid, acetic acid, and formic acid), and two strong electrolytes (Na2SO4 and H2SO4). The sorption equilibria in the studied system are complex because of three distinct sorption mechanisms: affinity-based interactions, site sharing, and ion exchange. Modelling of the sorption equilibria was attempted using simple sorption isotherms models: the Sheindorf–Rebuhn–Sheintuch (SRS), the Langmuir, and the Sips models. For simplicity, the electrolytes were treated as molecular components (without dissociation). In the case of pure carboxylic acids, both the SRS (residuals 10–5–10–4) and Sips models (residuals ∼ 10–7–10–5) correlated well with the experimental data. However, the Langmuir model was found to be inadequate. In the case of competitive sorption, the SRS model (residuals 10–6–10–4) correlated well with the data, but the Sips model’s (residuals ∼ 10–2) predicted sorption was too strong. Additionally, the sorption of Na2SO4 was well predicted by the SRS model. For each component pair, only a single interaction parameter was required with the SRS model. The sorption equilibria (SRS) model and the column mass balance model were validated against data from batch column experiments done with carboxylic acid-rich feed solutions. Pure water or aqueous carboxylic acid and salt solutions were used as eluents. The model accurately predicted the elution profiles in each case. The characteristic shapes of the carboxylic acid elution profiles with the effects resulting from competitive sorption were well accounted for. Strong sensitivity of the studied system towards changes in pH and H2SO4 concentration was observed.

Aqueous solutions of organic acids as effective solvents for levodopa extraction from Mucuna pruriens seeds

• Aqueous solutions of organic acids are promising substitutes for organic solvents. • Performance in the extraction of L-dopa from the seeds of M. Pruriens was assessed. • High purity and yields of L-dopa have been achieved with the investigated compounds. Levodopa is an amino acid commonly used in the treatment of Parkinson’s disease found in several plants, such as Mucuna pruriens . The extraction of levodopa from biomass has been achieved using methanol, ethanol:water mixtures in presence of ascorbic acid, chloroform in alkaline media, and acetonitrile. Aiming at finding more sustainable solvents and develop efficient extraction processes, in this work, aqueous solutions of carboxylic acids (acetic, propionic, citric, glycolic, and lactic acid) and (poly)alcohols (ethanol, ethylene glycol and glycerol) were studied for the extraction of levodopa from Mucuna pruriens seeds. An initial screening with aqueous solutions of these compounds (at 50 wt%) was conducted at 50 °C, with an extraction time of 90 min at a solid/liquid (biomass/solvent) ratio of 1:10. Based on these results, citric acid aqueous solutions were identified as the best solvent, and an experimental design was carried out to optimize the temperature (T), solid/liquid ratio (S:L) and concentration of acid (wt.%), with the following optimal extraction conditions found: T = 60 °C, S:L = 1:7 and concentration of acid at 58 wt%. Under these optimal conditions, an extraction efficiency of 9.2 ± 0.1 wt% of levodopa was achieved. The recovery of levodopa from the acidic aqueous solution was achieved using an ion exchange column, allowing the recovery of approximately 84% of levodopa. The solvent was shown to be reusable in three successive extraction cycles, with no significant losses in the extraction efficiency of levodopa. The results here obtained show that citric acid aqueous solutions can lead to the effective extraction of levodopa from seeds of Mucuna pruriens, serving as basis for the development of more effective and environmentally friendly processes to recover natural products with therapeutic properties.

Effect of Solvent on the Hydrodynamic Properties of Collagen.

In this study, the effect of solvent on the hydrodynamic properties of collagen extracted from tail tendons of young rats was researched. Collagen was dissolved in various aqueous carboxylic acid solutions, including acetic acid (AA), acetic acid with the addition of sodium chloride (AA/NaCl), formic acid (FA), lactic acid (LA), citric acid (CA), and also citrate buffer at pH = 3.7 (CB). The properties of collagen solutions at a concentration of 0.45 mg/mL were characterized based on the viscometric method. The reduced viscosity, intrinsic viscosity, and Huggins coefficient of collagen solutions and effect of solvent, temperature, and UV irradiation on these properties were investigated. Collagen solutions in acetic acid, acetic acid/NaCl, and citrate buffer were irradiated with UV light up to 1 h, and the viscosity of collagen solutions was measured. It was found that the organic acids used as solvent affected viscosity behavior, denaturation temperature, and stability of collagen solutions. The lowest values of studied parameters were obtained for the collagen solutions in acetic acid with the addition of sodium chloride. Thus, the effect of various aqueous carboxylic acid solutions on collagen solutions properties and denaturation temperature can also be affected by the sodium chloride addition. The results of this research can be crucial for the preparation of collagen solutions for both cosmetic and biomedical applications.

Understanding the effect of co-reactants on ketonization of carboxylic acids in the aqueous-phase pyrolysis oil of wood

Ketonization of carboxylic acids is one of the crucial reactions to produce sustainable bio-fuel and bio-chemicals from the pyrolysis oil of wood. Ketonization using different mixed solutions of carboxylic acids, furfural, and hydroxyacetone has been explored to understand the influence of co-feed reactants on the performance of ketonization of carboxylic acid over the selected CeZrOx catalyst. Furfural (7% in water) inhibited the catalytic activity for ketonization of acetic acid (20% solution) with reversible blocking of active sites, but for a mixed solution of hydroxyacetone (7%) and acetic acid (20%), both reactants influenced each other, resulting in very low conversions and slow and uncompleted recovery to 50% after removing hydroacetone from the mixture. For the mixed solution (20% acetic acid + 7% furfural + 7% hydroxyacetone in water), hydroxyacetone was the most reactive compound on CeZrOx and the conversions of reactants reached below 10%, due to the inhibition of co-existing carbonyl components. This work provides guidance for ketonization of carboxylic acids in the aqueous-phase pyrolysis oil.

Techniques for increasing the thermal stability of poly[(R)-3-hydroxybutyrate] recovered by digestion methods

This work deals with the thermal stability of poly[(R)-3-hydroxybutyrate] (PHB) obtained by different isolation methods. PHB was recovered from bacteria by digestion with three different reagents (acid, base, surfactant) and by chloroform extraction as a reference. Thermal stability of the samples was investigated by differential scanning calorimetry, isothermal degradation with hot press, and gel permeation chromatography and was compared with the stability of commercially available PHB. PHBs recovered by digestion with alkaline reagents were found to be thermally unstable, compared to the extracted polymer and the commercially available one. Two different techniques for stabilization of PHB obtained by digestion methods were tested wash with acid solution or addition of carboxylic acid or anhydride before heating. Both methods proved to significantly increase the thermal stability.

Protective properties of superhydrophobic coatings on copper and steel obtained by electrochemical method

Superhydrophobic coatings are obtained by cathodic deposition of copper or nickel on a copper plate with treatment with an ethanol solution of highest carboxylic acids with a long hydrocarbon radical simultaneously or sequentially. They are characterized by a contact angle of water wetting of the order of 155...160°.These coatings protect the copper substrate from corrosion in conditions of 100% humidity for 100...180 days, while maintaining the contact angle within 152…154°. There is no mass loss. The influence of the reversal of the current during electrolysis on the value of the contact angle of wetting is investigated. SEM images of superhydrophobic coatings are presented, indicating multilevel roughness. Superhydrophobic coating on carbon steel is obtained by cathodic deposition of nickel and subsequent surface treatment in an ethanol solution of myristic acid and annealing at 60° for two hours. The influence of the duration of electrolysis on the value of the contact angle of wetting is estimated. Its value is in the range of 151…154°. Exposure of a coated steel plate for 50 days in conditions of 100% humidity is characterized by the absence of weight loss and maintaining the contact angle up to 154°.