Influence of physico-chemical parameters of surface-active systems components for minimization of evaporation of hydrocarbon liquids

2021 ◽  
pp. 84-91
Author(s):  
O. Spaska ◽  
◽  
AV.L. Chumak ◽  
M.R. Maksymyuk ◽  
V.M. Rudenko ◽  
...  
Keyword(s):  
Chemical Interaction ◽  
Gas Permeability ◽  
Film Formation ◽  
Critical Concentration ◽  
Micelle Formation ◽  
Hydroxyl Groups ◽  
Protective Film ◽  
Hydrophilic Lipophilic Balance ◽  
Forming Characteristics ◽  
The Stability

Highly efficient stable aerated hydrophilic compositions containing fluorotensides and ultralight microdisperse systems using gas-filled glass, aluminosilicate and polymer microspheres have been developed. Designing the compositions of PAS based on the surface activity of surfactants, their solubility in water and the ability to bind water and the formation of hydrogen bonds between the components. The main condition for the stability of the coating when mixing the components - the chemical interaction between them and the formation of a system that does not dissolve in hydrocarbons and does not break down in terms of use. The best film-forming characteristics necessary for the operation of the coating (simultaneous reduction of surface tension and film formation) active substances (FPAR), the non-polar part of the molecules of which contains a fluorocarbon chain, so they are insoluble in hydrocarbons, well soluble in water and easily distributed on the surface of hydrocarbon liquids, creating a protective film. The choice of co-surfactants was based on the ability to stabilize hydrophilic films on the surface of hydrocarbons not only at favorable HLB, but also at the lowest, although higher than the critical concentration of micelle formation (CCM), concentrations for forming a mixed adsorption layer of increased strength. This surfactant was water-oil-soluble twin-80, which will significantly increase the hydrophilic part and enhance the stability of the PAS and the stability of the aerated system. The introduction of glass microspheres into the components of the system has significantly enhanced its strength and stability. In the study of the stability and gas permeability of the developed surfactant systems, it was found that the insulating ability of the coating increases with increasing hydrophilic-lipophilic balance of the system and due to chemical interaction between the carboxyl group of fluorotenside and hydroxyl groups of surfactants.

scholarly journals Novel polymer surfactants based on the branched silatrane-containing polyesters and polyethers

2019 ◽  
Vol 14 (5) ◽  
pp. 61-70 ◽  
Author(s):  
V. V. Istratov ◽  
V. I. Gomzyak ◽  
O. V. Yamskova ◽  
G. D. Markova ◽  
L. G. Komarova ◽  
...  
Keyword(s):  
Molecular Weight ◽  
Degree Of Substitution ◽  
Biologically Active ◽  
Hydroxyl Groups ◽  
Critical Micelle Concentrations ◽  
Surface Active Properties ◽  
Hydrophilic Lipophilic Balance ◽  
Surface Active ◽  
The Stability ◽  
Polymer Surfactants

Objectives. Biologically active polymeric surfactants are a new promising class of macromolecules that can find application in medicine, cosmetology, and agriculture. In this study, a number of new biologically active amphiphilic polymers based on branched silatrane-containing polyesters and polyethers were obtained, and their surface-active properties were investigated.Methods. The branched polymers were represented by polyethers and polyesters, obtained respectively via the anionic polymerization of 1,2-epoxypropanol or a combination of equilibrium polycondensation and ring opening polymerization. The polymers were modified with 3-isocyanopropylsilatrane and trimethylethoxysilane to obtain the amphiphilic compounds containing silatrane groups bonded to the polymer backbone by the urethane bond. The structure of the synthesized polymer silatranes was confirmed via nuclear magnetic resonance spectroscopy and gel permeation chromatography. The surface active properties of all the copolymers obtained were investigated in connection with their obvious amphiphilicity. In particular, the formation of micelles in aqueous solutions is such a property. The critical micelle concentrations were determined by a method of quenching the fluorescence of the polymers.Results. It was shown that the values of the critical micelle concentrations and the hydrophilic-lipophilic balance values of polymers determined by the Griffin equation correlate well with each other. A linear relationship between the hydrophilic-lipophilic balance and the critical micelle concentrations was established. At the same time, polyether-based polymers generally showed higher critical micelle concentrations than polyester-based polymers, although the hydrophilic-lipophilic balance values for polymers of different series, but with close degrees of substitution, were close. It was found that the use of all synthesized polymers as stabilizers of direct and reverse emulsions leads to an increase in the aggregative stability of both types of emulsions. The stability of emulsions depended both on the degree of substitution of peripheral hydroxyl groups of polymers by silatranes and on the molecular weight and structure of the branched block of polymers. The stability of direct emulsions increased for all polymers, while that of inverse emulsions decreased with an increasing degree of substitution of hydroxyl groups by silatranes. The increase of the branched block molecular weight led to an increase of droplet sizes for both direct and inverse emulsions. The smallest droplet size for direct and inverse emulsions was obtained using polymers with low molecular weight branched polyester blocks as surfactants.Conclusions. The results obtained prove the possibility of creating polymer surfactants containing silatrane groups. By varying the structure of the polymer, its molecular weight and the degree of substitution of peripheral functional groups, it is possible to obtain surfactants with desired surface properties.

scholarly journals Spilanthes acmella Leaves Extract for Corrosion Inhibition in Acid Medium

Coatings ◽  
2021 ◽  
Vol 11 (1) ◽  
pp. 106
Author(s):  
Akbar Ali Samsath Begum ◽  
Raja Mohamed Abdul Vahith ◽  
Vijay Kotra ◽  
Mohammed Rafi Shaik ◽  
Abdelatty Abdelgawad ◽  
...  
Keyword(s):  
Mild Steel ◽  
Corrosion Inhibition ◽  
Active Sites ◽  
Inhibition Efficiency ◽  
Electrochemical Impedance ◽  
Film Formation ◽  
Protective Film ◽  
Surface Protection ◽  
Tafel Polarization ◽  
Spilanthes Acmella

In the present study, the corrosion inhibition effect of Spilanthes acmella aqueous leaves extract (SA-LE) on mild steel was investigated in 1.0 M HCl solution at different temperature using weight loss, Tafel polarization, linear polarization resistance (LPR), and electrochemical impedance (EIS) measurements. Adsorption of inhibitor on the surface of the mild steel obeyed both Langmuir and Temkin adsorption isotherms. The thermodynamic and kinetic parameters were also calculated to determine the mechanism of corrosion inhibition. The inhibition efficiency was found to increase with an increase in the inhibitor concentration i.e., Spilanthes acmella aqueous leaves extract, however, the inhibition efficiency decreased with an increase in the temperature. The phytochemical constituents with functional groups including electronegative hetero atoms such as N, O, and S in the extract adsorbed on the metal surface are found responsible for the effective performance of the inhibitor, which was confirmed by Fourier-transform infrared spectroscopy (FT-IR) and ultraviolet–visible spectroscopic (UV-Vis) studies. Protective film formation against corrosion was confirmed by scanning electron microscopy (SEM), atomic force microscopy (AFM), and contact angle studies. The result shows that the leaves extract acts as corrosion inhibitor and is able to promote surface protection by blocking active sites on the metal.

Modeling of sorption kinetics of U(VI) micro-quantities nanostructured materials with anatase mesoporous structures

2021 ◽  
Vol 0 (0) ◽  
Author(s):  
Veniamin Zheleznov ◽  
Aleksey Golikov ◽  
Tatiana Sokolnitskaya ◽  
Sergey Ivannikov
Keyword(s):  
Nanostructured Materials ◽  
Sorption Kinetics ◽  
Uranyl Ion ◽  
Competitive Sorption ◽  
Hydroxyl Groups ◽  
Complex Ions ◽  
The Stability ◽  
Kinetics Of ◽  
Mesoporous Structures ◽  
Ionic Forms

Abstract The sorption kinetics of uranyl ions micro-quantities from fluoride solutions by nanostructured materials with anatase mesoporous structures has been studied. Using the model of competitive sorption of ions and positively charged complexes of uranyl ion on deprotonated hydroxyl groups of an anatase, kinetic curves of changes in the ratio of ionic forms of uranium in solution were calculated. Modeling was carried out under the assumption of a two-stage mechanism of uranium complex ions sorption. The modeling considered the influence of the uranyl ion carbonate complexes formation. The shift in equilibrium among ionic forms of uranyl correlates with the stability of the complexes in solution.

scholarly journals Comparison Between the Action of Nano-Oxides and Conventional EP Additives in Boundary Lubrication

Lubricants ◽  
2020 ◽  
Vol 8 (5) ◽  
pp. 54
Author(s):  
Valdicleide Silva Mello ◽  
Marinalva Ferreira Trajano ◽  
Ana Emilia Diniz Silva Guedes ◽  
Salete Martins Alves
Keyword(s):  
Friction Coefficient ◽  
Boundary Lubrication ◽  
Friction And Wear ◽  
Film Formation ◽  
Environmental Issues ◽  
Protective Film ◽  
Extreme Pressure ◽  
Extreme Pressure Additives ◽  
Environmental Requirements ◽  
Lubrication Conditions

Additives are essential in lubricant development, improving their performance by the formation of a protective film, thus reducing friction and wear. Some such additives are extreme pressure additives. However, due to environmental issues, their use has been questioned because their composition includes sulfur, chlorine, and phosphorus. Nanoparticles have been demonstrated to be a suitable substitute for those additives. This paper aims to make a comparison of the tribological performance of conventional EP additives and oxides nanoparticles (copper and zinc) under boundary lubrication conditions. The additives (nanoparticles, ZDDP, and sulfur) were added to mineral and synthetic oils. The lubricant tribological properties were analyzed in the tribometer HFRR (high frequency reciprocating rig), and during the test, the friction coefficient and percentual of film formation were measured. The wear was analyzed by scanning electron microscopy. The results showed that the conventional EP additives have a good performance owing to their anti-wear and small friction coefficient in both lubricant bases. The oxides nanoparticles, when used as additives, can reduce the friction more effectively than conventional additives, and displayed similar behavior to the extreme pressure additives. Thus, the oxide nanoparticles are more environmentally suitable, and they can replace EP additives adapting the lubricant to current environmental requirements.

scholarly journals Probing the Effect of Titanium Substitution on the Sodium Storage in Na3Ni2BiO6 Honeycomb-Type Structure

Energies ◽  
2020 ◽  
Vol 13 (24) ◽  
pp. 6498
Author(s):  
Eugen Zemlyanushin ◽  
Kristina Pfeifer ◽  
Angelina Sarapulova ◽  
Martin Etter ◽  
Helmut Ehrenberg ◽  
...  
Keyword(s):  
Critical Concentration ◽  
Sol Gel ◽  
Honeycomb Structure ◽  
Electrochemical Process ◽  
Electrochemical Kinetics ◽  
Fast Diffusion ◽  
Reversible Phase Transition ◽  
Synchrotron Radiation Diffraction ◽  
Na Ions ◽  
The Stability

Na3Ni2BiO6 with Honeycomb structure suffers from poor cycle stability when applied as cathode material for sodium-ion batteries. Herein, the strategy to improve the stability is to substitute Ni and Bi with inactive Ti. Monoclinic Na3Ni2-xBi1-yTix+yO6 powders with different Ti content were successfully synthesized via sol gel method, and 0.3 mol of Ti was determined as a maximum concentration to obtain a phase-pure compound. A solid-solution in the system of O3-NaNi0.5Ti0.5O2 and O3-Na3Ni2BiO6 is obtained when this critical concentration is not exceeded. The capacity of the first desodiation process at 0.1 C of Na3Ni2BiO6 (~93 mAh g−1) decreases with the increasing Ti concentration to ~77 mAh g−1 for Na3Ni2Bi0.9Ti0.1O6 and to ~82 mAh g−1 for Na3Ni0.9Bi0.8Ti0.3O6, respectively. After 100 cycles at 1 C, a better electrochemical kinetics is obtained for the Ti-containing structures, where a fast diffusion effect of Na+-ions is more pronounced. As a result of in operando synchrotron radiation diffraction, during the first sodiation (O1-P3-O’3-O3) the O’3 phase, which is formed in the Na3Ni2BiO6 is fully or partly replaced by P’3 phase in the Ti substituted compounds. This leads to an improvement in the kinetics of the electrochemical process. The pathway through prismatic sites of Na+-ions in the P’3 phase seems to be more favourable than through octahedral sites of O’3 phase. Additionally, at high potential, a partial suppression of the reversible phase transition P3-O1-P3 is revealed.

scholarly journals PECULARITIES OF MICELLE FORMATION OF PENTACYCLIC GLYCOSIDES IN AQUEOUS SOLUTIONS

2021 ◽  
Vol 64 (4) ◽  
pp. 26-33
Author(s):  
Natalia V. Mironenko ◽  
Irina V. Shkutina ◽  
Vladimir F. Selemenev
Keyword(s):  
Surface Tension ◽  
Light Scattering ◽  
Dynamic Light Scattering ◽  
Aqueous Solutions ◽  
Hydrodynamic Radius ◽  
Critical Concentration ◽  
Micelle Formation ◽  
Cylindrical Shape ◽  
Scattering Method ◽  
Dynamic Light Scattering Method

The regularities of changes in structural characteristics during the formation of associates in micellar aqueous solutions of triterpene saponins Quillaja Saponin and Sapindus Mukorossi are considered. The dependence of surface tension and adsorption on the concentration of an aqueous saponin solution is analyzed, and the values of surface activity and parameters of the adsorption layer are calculated. The average values of diffusion coefficients for spherical and cylindrical micelles are determined based on the measurement of the solution viscosity. The effect of the electrolyte solution on the surface tension and viscosity of glycoside solutions is studied: when the electrolyte is introduced into the saponin solution, the surface tension decreases, which leads to a shift in the critical concentration of micelle formation towards lower concentrations. The introduction of potassium chloride electrolyte reduces the degree of ionization and, as a result of suppressing the electroviscosity effect, leads to a decrease in the viscosity of the solution. The dynamic light scattering method is used to determine the size of glycoside aggregates. It is established that there are aggregates of several sizes in an aqueous solution of saponin. The size and shape of aggregates were calculated using the concepts of micelle packing parameters. In the region of very low concentrations of glycoside solutions, when approaching the critical concentration of micelle formation in the solution, there are spherical micelles. A further increase in the saponin concentration in the solution leads to a decrease in the content of structures with a hydrodynamic radius of 50-80 nm and the appearance of larger agglomerates with sizes greater than 100 nm. It was found that micelles acquire a less hydrated and more densely packed cylindrical shape in the concentration range of 1.7-2.6 mmol/dm3. Compaction of associates leads to an increase in the content of particles with a hydrodynamic radius of 150-250 nm and larger ones, and their presence predicts the appearance of larger agglomerates. Analyzing the data obtained using the dynamic light scattering method, it can be concluded that aggregates of several sizes co-exist in the volume of aqueous saponin solutions at certain concentrations.

scholarly journals Critical Concentration of Lecithin Enhances the Antimicrobial Activity of Eugenol against Escherichia coli

2017 ◽  
Vol 83 (8) ◽  
Author(s):  
Haoshu Zhang ◽  
Edward G. Dudley ◽  
P. Michael Davidson ◽  
Federico Harte
Keyword(s):  
Escherichia Coli ◽  
Essential Oils ◽  
Food Systems ◽  
Critical Concentration ◽  
Physical Stability ◽  
Antimicrobial Properties ◽  
Content Type ◽  
Antimicrobial Effects ◽  
Wide Range ◽  
The Stability

ABSTRACT Lecithin is a natural emulsifier used in a wide range of food and nonfood applications to improve physical stability, with no known bioactive effects. In this study, the effect of lecithin on the antimicrobial performance of a constant eugenol concentration was tested against three Escherichia coli strains (C600, 0.1229, and O157:H7 strain ATCC 700728). This is the first study, to our knowledge, focusing on lecithin at concentrations below those commonly used in foods to improve the stability of oil in water emulsions (≤10 mg/100 ml). For all three cultures, significant synergistic antimicrobial effects were observed when E. coli cultures were exposed to a constant eugenol concentration (ranging from 0.043 to 0.050% [wt/wt]) together with critical lecithin concentrations ranging from 0.5 to 1 mg/100 ml. Increasing the concentration of lecithin above 1 mg/100 ml (up to 10 mg/100 ml lecithin) diminished the antibacterial effect to values similar to those with eugenol-only treatments. The formation of aggregates (<100 nm) at the critical lecithin concentration was observed using cryo-transmission electron microscopy (cryo-TEM), together with a reduction in light absorbance at 284 nm. At critically low concentrations of lecithin, the formation of nanoscale aggregates is responsible for improving eugenol antimicrobial effects. IMPORTANCE Essential oils (EOs) are effective natural antimicrobials. However, their hydrophobicity and strong aromatic character limit the use of essential oils in food systems. Emulsifiers (e.g., lecithin) increase the stability of EOs in water-based systems but fail to consistently improve antimicrobial effects. We demonstrate that lecithin, within a narrow critical concentration window, can enhance the antimicrobial properties of eugenol. This study highlights the potential bioactivity of lecithin when utilized to effectively control foodborne pathogens.

Active surface centres in vanadium pentoxide/alkali metal sulphate heterogeneous catalysts for 2-propanol decomposition

1979 ◽  
Vol 57 (18) ◽  
pp. 2464-2469 ◽  
Author(s):  
David Victor Fikis ◽  
William John Murphy ◽  
Robert Anderson Ross
Keyword(s):  
Alkali Metal ◽  
Surface Area ◽  
Vanadium Pentoxide ◽  
Heterogeneous Catalysts ◽  
Catalyst Activity ◽  
Active Surface ◽  
Hydroxyl Groups ◽  
Kinetic Measurements ◽  
The Stability ◽  
The Individual

Infrared spectra of the surfaces of vanadium pentoxide and vanadium pentoxide containing 9.09 mol% caesium and potassium, as sulphates, have been determined after exposure to 2-propanol for various times. Interpretation of the spectra leads to the proposal that the principal source of catalyst activity may be associated with surface hydrogen and hydroxyl groups on V5+ and V4+ sites. The "stability" of the catalysts towards reduction by the alcohol was consistent with the activity series derived from kinetic measurements: V2O5 (pure) < V2O5 (Cs) < V2O5 (K). The degree of sample reduction has also been assessed qualitatively by measurements of the ratio of surface area before to that after reaction and the same catalyst sequence was established. The trend in surface area ratios was similar to that shown by the surface "Tammann" temperatures of vanadium pentoxide and alkali metal sulphates which has been taken to imply that the ease and (or) extent with which the sulphates enter into inter-solid reactions with the oxide in the preparation stage may exert influence on the subsequent reducibility of the individual members of the catalyst series.

Control by Mixed-Chloride Additives of the Quality and Homogeneity of Bulk Halide Perovskite upon Film Formation Process

2021 ◽  
Author(s):  
Thierry Pauporté ◽  
Daming zheng
Keyword(s):  
Solar Cells ◽  
Formation Process ◽  
High Efficiency ◽  
Film Formation ◽  
Perovskite Solar Cells ◽  
X Ray Diffraction ◽  
X Ray ◽  
Stability Issue ◽  
Halide Perovskite ◽  
The Stability

Nowadays, overcoming the stability issue of perovskite solar cells (PSCs) while keeping high efficiency has become an urgent need for the future of this technology. By using x-ray diffraction (XRD),...

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