Contact Angle Method Research Articles

Correlation of surface properties with dissolution behavior of amorphous solid dispersion of Riluzole and its pharmacodynamic evaluation

Formulation of amorphous solid dispersion (ASD) of any poorly water-soluble drug is among the most promising techniques to increase the dissolution profile of drug and hence its bioavailability. Various literatures give evidences of the role of drug-polymer interactions in the ASD systems, very little information is available about the surface properties of the drug molecule and their ASDs which contributes to a higher dissolution profile. Current work focuses on exploring the surface behavior of a poorly water-soluble drug Riluzole (RLZ) and its ASDs prepared with two highly hydrophilic polymers, polyacrylic acid (PAA), and polyvinylpyrrolidone vinyl acetate (PVP VA). Initial characterization using X-ray diffraction (XRD) revealed about the weight fraction of drug required to prepare a single-phase homogenous system with both the polymers. The saturation solubility and the dissolution studies showed an increase in RLZ solubility as well as the dissolution profile due to the presence of polymers. The role of polymers in changing the surface properties in terms of wettability and polarity were explored using contact angle method and X-ray photon spectroscopy (XPS). Additionally, the neuroprotective efficacy and dose dependent hepatotoxicity were also evaluated in male wistar rats. These studies confirmed the increase in the surface polarity and hence the enhanced ability of ASD formulations to interact with water. The in vivo studies indicated that at the current recommended dose the efficacy as well as toxicity is increased for the ASD formulation. Hence, this formulation can be given at a lower dose to achieve same therapeutic effect with lower toxicity.

Investigation of mechanical and wettability properties of commercial pure titanium by surface mechanical attrition treatment

The examination of mechanical and wettability properties of commercial pure titanium (CP-Ti) introduced a novel challenge. The microstructure of samples was analyzed by using OM and SEM micro-images. In this study, the hardness of the surface and cross section of samples was evaluated, and the effect of several surface mechanical attrition treatments (SMATed) on samples was examined. Also, the tensile test was done to compare the effect of SMAT duration on mechanical properties of samples. The contact angle method was then employed to investigate the impact of SAMT duration on the wettability trend. According to results, as the treatment time increases, twins become evident in the deeper layers of the samples. In contrast, the near-surface twins are shorter than those found in the deeper material, signifying the presence of finer grains. Moreover, the elevated hardness in SMATed samples can be attributed to several key factors, including cold work, a rise in defects and twins, and grain refinement. The surface hardness increases across the sample series (up to Ti6) due to the substantial energy input. Nevertheless, it is anticipated that further continuation of the process will result in a constant surface hardness. The increased strength observed in SMATed samples can be attributed to factors such as reduction in grain size and the formation of twins. The wettability results show that the treated surfaces exhibited a significant change in wettability compared to the untreated samples, with a 25% reduction in the contact angle. This is attributed to the surface modifications induced by the treatment process, which introduced more hydrophilic functional groups. The results also show that after 4 h of treatment, the contact angle increases, suggesting that the trend may plateau with additional treatment time.

Eco-friendly corrosion inhibitor of Q235 carbon steel in 1.0 M HCl by Isatin/Chitosan Schiff base

This study presents the synthesis of an eco-friendly and green Schiff base, namely Isatin-Cs Schiff base corrosion inhibitor for Q235 carbon steel in 1.0 M HCl corrosion solution. Fourier-transformed infrared FT-IR and 1H NMR was utilized to characterize the prepared Isatin-Cs Schiff base corrosion inhibitor. The inhibition performance in 1.0 M HCl solution was investigated via classic weight loss at various temperatures, potentiodynamic polarization (PPD), and electrochemical impedance spectroscopy (EIS). Scanning electron microscopy SEM, X-ray photoelectron spectroscopy XPS, and water contact angle methods are used to analyze the surface morphology of Q235 carbon steel. The polarization measurements indicate that the corrosion inhibitors act as mixed type. Moreover, the weight loss studies show that the efficiency of inhibitor increases with the concentration of inhibitor to reach a maximum efficiency of 88.4 % with 250 ppm at 25 °C. Nevertheless, increasing temperature has negative effect on the efficiency of the Isatin-Cs inhibitor. The Langmuir isotherm Unveil that Isatin-Cs adsorption on Q235 carbon steel is mediated via physi/chemi-sorption. Based on SEM and XPS analyses Isatin-Cs forms stable protective film on Q235 carbon steel. The DFT results complemented the experiments results, both observed the effectiveness of inhibitor adsorption.

X-ray characterization, structural analysis, antibacterial activity, and self-cleaning property of Cu-doped TiO2-SiO2 nanocomposite prepared by sonochemical process

TiO2-SiO2 nanocomposites with different copper (Cu) precursor loadings were prepared by a one-step sonochemical process. The mole ratio of Cu precursor in TiO2-SiO2 composite was varied at 0.004, 0.008, 0.020, and 0.040, respectively. The specific X-ray characterization techniques on crystalline structure, chemical composition, and chemical states of Cu-doped TiO2-SiO2 composite were carried out by X-ray diffraction technique (XRD), X-ray fluorescence (XRF), and X-ray photoelectron spectroscopy (XPS), respectively. Surface morphology and chemical bonding of Cu-doped TiO2-SiO2 composite were monitored by field emission scanning electron microscope (FE-SEM) and Fourier transform infrared spectrophotometer (FTIR). For antibacterial properties, the inhibition zone of antimicrobial activity was investigated by varying amounts of Cu precursors in the TiO2-SiO2 composite. After that, Cu-doped TiO2-SiO2 composite powder with different Cu precursor ratios was mixed in PMMA solution and deposited on glass slides to study the optical property and hydrophilicity by UV-VIS-NIR spectrophotometer and contact angle method. XRD patterns of Cu-doped TiO2-SiO2 nanocomposites show the formation of the main TiO2 anatase phase with the ultrafine particles observed by FE-SEM images. FT-IR spectra of the composites are assigned to the prominent peaks of the Ti-O-Ti and Ti-O-Si bond relating to the TiO2-SiO2 host matrix. Meanwhile, TiO2-SiO2 composites with Cu precursor at 0.004 mol ratio can significantly enhance the antibacterial activity with a large inhibition zone. The contact angle value of Cu-doped TiO2-SiO2 nanocomposite film at 0.040 Cu precursor mole ratio in the TiO2-SiO2 matrix resulted in the optimized composite ratio for achieving a hydrophilic surface on the substrate.

The effect of Dunaliella salina extracts on the adhesion of Pseudomonas aeruginosa to 3D printed polyethylene terephthalate and polylactic acid

Polyethylene terephthalate (PET) and polylactic acid (PLA) are among the polymers used in the food industry. In this study, crude extracts of Dunaliella salina were used to treat the surface of 3D printed materials studied, aiming to provide them with an anti-adhesive property against Pseudomonas aeruginosa. The hydrophobicity of treated and untreated surfaces was characterized using the contact angle method. Furthermore, the adhesive behavior of P. aeruginosa toward the substrata surfaces was also studied theoretically and experimentally. The results showed that the untreated PLA was hydrophobic, while the untreated PET was hydrophilic. It was also found that the treated materials became hydrophilic and electron-donating. The total energy of adhesion revealed that P. aeruginosa adhesion was theoretically favorable on untreated materials, while it was unfavorable on treated ones. Moreover, the experimental data proved that the adhesion to untreated substrata was obtained, while there was complete inhibition of adhesion to treated surfaces.

Experimental Investigation of the Impact of CO2 Injection Strategies on Rock Wettability Alteration for CCS Applications

Carbon capture and storage (CCS) has been recognized as a pivotal technology for mitigating climate change by reducing CO2 emissions. Storing CO2 in deep saline aquifers requires preserving the water-wet nature of the formation throughout the storage period, which is crucial for maintaining rock integrity and storage efficiency. However, the wettability of formations can change upon exposure to supercritical CO2 (scCO2), potentially compromising storage efficiency. Despite extensive studies on various factors influencing wettability alteration, a significant research gap remains in understanding the effects of different CO2 injection strategies on wettability in deep saline formations (DSFs). This study addresses this gap by investigating how three distinct CO2 injection strategies—continuous scCO2 injection (CCI), water alternating with scCO2 injection (WAG), and simultaneous water and scCO2 injection (SAI)—affect the wettability of gray Berea sandstone and Indiana limestone, both selected for their homogeneous properties relevant to CCS. Using a standardized sessile drop contact angle method before and after CO2 injection, along with core flooding to model the injection process at an injection pressure of 1500 psi and temperature of 100 °F with a confining pressure of 2500 psi, the results indicate a shift in wettability towards more CO2-wet conditions for both rock types under all strategies with changes in CA of 61.6–83.4° and 77.6–87.9° and 81.5–124.2° and 94.6–128.0° for sandstone and limestone, respectively. However, the degree of change varies depending on the injection strategy: sandstone exhibits a pronounced response to the CCI strategy, with up to a 77% increase in contact angle (CA), particularly after extended exposure. At the same time, WAG shows the least change, suggesting that water introduction slows surface modification. For limestone, the changes in CA ranged from 9% to 49% across strategies, with WAG and SAI being more effective in altering its wettability. This study underscores the importance of selecting suitable CO2 injection strategies based on rock type and wettability characteristics to maximize carbon storage efficiency. The findings offer valuable insights into the complex interactions of fluid–rock systems and a guide for enhancing the design and implementation of CCS technologies in various geological settings.

Indicative significance of the interfacial interactions between pore surface and soluble organic matter on the shale oil mobility

The exploration and exploitation of shale oil resources enhance the necessity to characterize the mobility of the occluded oil in shales. Up to now, the understanding of the controlling factors of shale oil mobility has mainly come from molecular dynamics simulation but lacking in-depth research on actual shales. Therefore, in this study, the effects of mineral composition, soluble organic matter (SOM) composition and wettability on the shale oil mobility were studied by X-ray diffraction, N2 adsorption, mercury intrusion, contact angle, chloroform bitumen and group component detection methods, comprehensively. The results show that: (1) The asphaltene contents and (Asphaltenes × Aromatics)/(Saturates × Resins) negatively and positively correlate with clay and carbonate mineral contents, respectively, while the I/S and illite contents present opposite trend with (Asphaltenes × Aromatics)/(Saturates × Resins). These correlations indicate that the SOM that confined in the pores constructed with carbonate minerals and illite present better flow potential. (2) Both δVt and δSSA negatively correlate with asphaltenes and (Asphaltenes × Aromatics)/(Saturates × Resins). That is, less pores and surfaces can be released by extraction for the shales with more asphaltenes. Therefore, it can be concluded that asphaltene is a negative factor for shale oil seepage. Additionally, the larger pores present better flow condition for shale oil, even for asphaltenes. (3) Pore surface wettability also significantly affects the shale oil mobility. The hydrophobicity of the pore wall greatly inhibits the shale oil flow, especially for the mesopores and macropores. The pattern diagram was established to illustrate the effect of the interactions between pore surfaces and shale oil components on the movable potential. Based on our research, mineral composition, group composition and pore surface wettability are efficient parameters for the shale oil mobility evaluation based on the interfacial interaction theory, and the “sweet spots” for shale oil seepage of the Jiyang Depression are the shales with more illite, carbonate, saturates and relatively low lipophilicity.

Pluronic P123/DMSO Lyotropic Liquid Crystal for Incorporating Bioactive Substances for Topical Application.

Lyotropic liquid crystals (LLCs) have attracted considerably growing interest in drug delivery applications over the last years. The structure of LLC matrices is complementary to cell membranes and provides an efficient, controlled, and selective release of drugs. In this work, a complex of experimental methods was used to characterize binary LLCs Pluronic P123/DMSO and triple LLC systems Pluronic P123/DMSO/Ibuprofen, which are interesting as transdermal drug delivery systems. Liquid crystalline, thermal, and rheological properties of LLCs were studied. Concentration and temperature areas of the lyomesophase existence were found, and phase transition enthalpies were evaluated. Intermolecular interactions among the components were studied by infrared (IR) spectroscopy. In vitro studies of Ibuprofen (Ibu) release from various LLCs allow differentiation of its release depending on the polymer content. Atomic force microscopy and contact angle methods were used to characterize the surface morphology of the hydrophobic membrane, which was used as a stratum corneum model, and also evaluate the adhesion work of the LLCs. A complex analysis of the results provided by these experimental methods allowed revealing correlations between the phase behavior and rheological characteristics of the LLCs and release kinetics of ibuprofen. The proposed biocompatible systems have considerable potential for a transdermal delivery of bioactive substances.

Antimicrobial and antiadhesive activities of secondary metabolites against Bacillus cereus adhesion on PLA 3D printing material: ADMET Tox in silico, molecular docking and molecular dynamic analysis

Bioactive compounds are naturally occurring substances that have the ability to have physiological impacts on the human body. Due to their potential health advantages and their function in preventing and treating a variety of serious health risks, also this substances shown a high antibacterial and antibiofilm activities against bacteria that can affect health. Therefore, the purpose of the current investigation was to test different bioactive compounds (Thymol, Quercetin, Epicatechin gallate, Gallic acid, Coumarin, Caffeic acid, Tannic acid, Apigenin, Carvacrol, Carvone, Beta ionone and Eucalyptol), in order to see there effect against B. cereus. Additionally, the contact angle method was used to examine the influence of those substances on the physicochemical characteristics of PLA 3D printing material and there antiadhesive effect against bacteria studied. According to the antibacterial activities it should be noted that Carvacrol, Tannic acid and Epicatechin gallate were the most active against B. cereus bacteria. The measurements of the contact angle showed a substantial change in the physicochemical characteristics of 3D printing PLA, indicating an improvement in the electron donor character after treatment, and significantly changed the surface hydrophobicity following treatment from hydrophobe PLA to hydrophile PLA after treatement, we can also see that B. cereus can adhere to PLA before treatment but after treatment with bioactive compounds it has become unfavorable which means that our select compounds are indeed active. After the use of computational methods like ADMET analysis, molecular docking and dynamic analysis, it was practical to better understand the physicochemical and pharmacokinetic proprieties, drug-likeness, antibacterial antiadhesive properties of the studied phytocomponents.

Computational aptamer design for spike glycoprotein (S) (SARS CoV-2) detection with an electrochemical aptasensor

A new bioinformatic platform (APTERION) was used to design in a short time and with high specificity an aptamer for the detection of the spike protein, a structural protein of SARS-CoV-2 virus, responsible for the COVID-19 pandemic. The aptamer concentration on the carbon electrode surface was optimized using static contact angle and fluorescence method, while specificity was tested using differential pulse voltammetry (DPV) associated to carbon screen-printed electrodes. The data obtained demonstrated the good features of the aptamer which could be used to create a rapid method for the detection of SARS-CoV-2 virus. In fact, it is specific for spike also when tested against bovine serum albumin and lysozyme, competitor proteins if saliva is used as sample to test for the virus presence. Spectrofluorometric characterization allowed to measure the amount of aptamer present on the carbon electrode surface, while DPV measurements proved the affinity of the aptamer towards the spike protein and gave quantitative results. The acquired data allowed to conclude that the APTERION bioinformatic platform is a good method for aptamer design for rapidity and specificity.Key points• Spike protein detection using an electrochemical biosensor• Aptamer characterization by contact angle and fluorescent measurements on electrode surface• Computational design of specific aptamers to speed up the aptameric sequence time

Accurate measurement method of contact angle within a small angle

The wetting phenomenon of liquid on a solid surface is a fundamental natural phenomenon in nature. It has a significant impact on people’s production and life. This paper solves the problem that small-angle wetting cannot be accurately measured by changing the imaging direction and complete auxiliary methods.

Nuclear magnetic resonance study on wettability of shale oil reservoir

In order to identify and evaluate reservoir wettability, so as to select suitable mining methods to improve oil recovery, wettability evaluation through one-dimensional (1D) and two-dimensional (2D) nuclear magnetic resonance (NMR) technology combined with physical simulation experiments was carried out in this study, and the feasibility of the experimental method was verified by contact Angle method. According to the principle of hydrophilic inorganic content and hydrophobic organic content of shale, the wettability can be evaluated through vacuum self-imbibition oil and self-imbibition water physical simulation experiments combined with 1D NMR technology, that is, total water absorption can be considered as inorganic content, organic content can be obtained by subtracting total water absorption from total oil absorption, and adsorbed oil content can be obtained by subtracting pore volume from total oil absorption. In addition to the wettability measurement by contact Angle method to verify the experimental method, the occurrence ratio of adsorbed oil can also be verified twice by 2D NMR spectrum. The results show that the error between the proportion of adsorbed oil measured by 2D NMR spectrum and that measured by self-imbibition method is within 4%. In the saturated oil-bound water state, the bound water is within the relaxation interval of 1<T1<10 ms and 1<T2<10 ms, and the oil signal is within the relaxation interval of T1>10 ms and T2>10 ms. And the relaxation time of aqueous phase moved to the right compared with that in the saturated water state, the interaction force between water and the pore wall was weakened, showing the characteristics of free fluid, and the rock sample became oil-wet, which was consistent with the wettability results measured by contact Angle. Therefore, the wettability of rock samples can be evaluated by 1D NMR technique combined with vacuum imbibition method, or by analyzing the changes of NMR spectra of aqueous phase in completely saturated water and saturated oil-bound water.

Evaluation of rock and fluid intermolecular interaction between asphaltene and sand minerals using electrochemical, analytical spectroscopy and microscopy techniques

Long-time contact of heavy crude oil with rock leads to an adsorption phenomenon, which causes the rock surface to become oil-wet and appears as a barrier to the fluid flow in the porous media. However precise understanding of how asphaltene fractions influence sand wettability is lacking. The wetness of neat and asphaltene-aged sandstone was calculated using two relative permeability and contact angle methods. Then the molecular interaction between asphaltene and sand minerals was systematically analyzed using Fourier-transform infrared spectroscopy. Furthermore, the zeta potential was representative of electrostatic properties and surface charge alteration of the sand after these phenomena. Scanning electron microscopy with energy-dispersive X-ray (EDX) analysis also showed elemental mapping and dispersion of asphaltene particles on the rock surface. According to contact angle and EDX analyses of asphaltene samples, the contact angle rises from 115° to 141° by an increase in carbon adsorption on the sand surface from 8.23 to 41.56%. Spectroscopy results demonstrated that hydrogen-bonding, π-bonding, and sulfur-containing compounds such as sulfoxide improve asphaltene adsorption onto the sand surface. The higher the aromaticity index and hydrogen potential index of asphaltene, the greater the ability of asphaltene to change wettability. Adsorption of surface active components would make the surface charge of the sand more negative. The presence of nitrogen/sulfur-containing functional groups on the sand surface changed the electrostatic properties, as a sand surface coated with asphaltene would reduce the percentage of metal cations.

Preparation and application of stimuli-responsive PET TeMs: RAFT graft block copolymerisation of styrene and acrylic acid for the separation of water-oil emulsions.

Stimuli-responsive membranes play an important role in the fields of biomedicine, food and chemical industries, and environmental applications, including separation of water-oil emulsions. In this study, we present a method to fabricate pH-sensitive membranes using UV-initiated RAFT graft copolymerization of styrene (ST) and acrylic acid (AA) on poly(ethylene terephthalate) (PET) track-etched membranes (TeMs). The optimization of polymerization conditions led to successful grafting of polystyrene (PS) and poly(acrylic acid) (PAA) onto PET TeMs, resulting in membranes with stable hydrophobicity and pH change responsiveness. The membranes show a contact angle of 65° in basic environments (pH 9) and 97° in acidic environments (pH 2). The membranes were characterized by atomic force microscopy (AFM), scanning electron microscopy with energy dispersive X-ray spectroscopy (SEM-EDX), thermogravimetric analyses (TGA), Fourier transform infrared spectroscopy (FTIR), contact angle (CA) methods. The PET TeMs-g-PS-g-PAA exhibited good performance in separating water-oil emulsions with a high efficiency of more than 90% and flux for direct chloroform-water 2500 L m-2 h-1 and reverse emulsions of benzene-water 1700 L m-2 h-1. This method of preparing stimuli-responsive membranes with controlled wettability and responsiveness to environmental pH provides versatility in their use in separating two types of emulsions: direct and reverse.

Optimization of PDMS Surface Treatment Using Atmospheric Pressure Plasma for Microfluidic Applications

Abstract Polydimethylsiloxane (PDMS) is widely used for microfluidic and biomedical applications because of its chemical inertness and affordability. However, its low surface energy limits its adhesion properties, thus necessitating mandatory surface activation, via plasma treatments or chemical processing, especially for improving its hydrophilicity. In this study, we employed an atmospheric pressure plasma jet (2 W) in order to enhance the PDMS surface adhesion for application in microfluidic devices. Treatment variables, including exposure and recovery time and adhesion quality, were investigated. It was possible to achieve a minimum exposure time of 15 s/cm2 for thin PDMS (sheet, 250 μm) and 30 s/cm2 for thick (resin, 3 mm) PDMS. A robust and efficient methodology for scaling the jet system treatment of larger areas was developed. Additionally, we examined the effect of ambient humidity on the plasma treatment. Results showed that water adsorption on PDMS-treated surfaces indicated a difference between the well-established contact angle method for determining surface hydrophilicity (and thus, its adhesion) and the real adhesion properties of the treated surfaces.

Evaluation of the hydrophobic and barrier properties of the polyurethane coatings covered by stearic acid thin layer

In this paper, a thin stearic acid (SA) film was deposited onto the polyurethane (PU) coatings with different concentrations of stearic acid in the ethanol (1 wt.%, 2 wt.% and 3 wt.%) by centrifuged technique. Fourier transform infrared spectra (FTIR) and water contact angle (WCA) method were performed to characterize and evaluate the hydrophobic layer formed on the surface of the samples. Then, the barrier property of the PU/SA was assessed by using electrochemical impedance spectroscopy (EIS) and accelerated salt spray test method. The results show that the presence of the stearic acid layer was effective for both hydrophobic and barrier properties, especially the samples prepared with 3 wt.% stearic acid. This work landmarks the need for improving the protection ability of polyurethane coatings for a metallic substrate.

Characterization and in vitro bioactivity evaluation of polyvinyl alcohol incorporated electro spun chitosan/ fluor apatite nanofibrous scaffold for bone tissue engineering

In this study, polyvinyl alcohol/chitosan/fluor apatite scaffolds with different concentrations of polyvinyl alcohol of 0.075 g ml−1 and 0.1 g ml−1, respectively named A and B fabricated by electrospinning method to use in tissue engineering. By examining the scaffolds by FE-SEM, an appetite layer formation which was on the scaffold surface was clearly observable. Increasing the concentration of polyvinyl alcohol from 0.075 g ml−1 to 0.1 g ml−1 in the nanofibrous scaffolds improved degradation characteristic with an optimized value of 26 ± 2 and 42 ± 1 % after 28 days, respectively. The mean diameter of fibers both scaffolds was 405 nm and 212 nm, respectively. Furthermore, the percentage of porosity in both scaffolds was calculated as 84% and 91%, separately. The level of hydrophilicity of the scaffolds was measured by the dynamic contact angle method. Moreover, the increase in the percentage of polyvinyl alcohol led to the decrease in the average contact angle in scaffold A and scaffold B from 90° to 70°, respectively. The results of bone marrow culture test with MG-63 (NCBI C555) cell on the surface of scaffolds demonstrated not cytotoxicity in the resulting scaffolds as well as a suitable substrate for the adhesion and growth of the cells. According to our findings, the electrospun fluorapatite-incorporated-chitosan/polyvinyl alcohol scaffold could provide a new nanocomposite for biomedical applications.

Anticorrosion studies of 5-acetyl-4-(3-methoxyphenyl)-6-methyl-1-phenyl-3,4-dihydropyrimidin-2(1H)-one: approach from experimental, DFT studies, and MD simulation

Abstract The effectiveness of 5-acetyl-4-(3-methoxyphenyl)-6-methyl-1-phenyl-3,4-dihydropyrimidin-2(1H)-one as a corrosion inhibitor for mild steel in acidic conditions was investigated herein through the experimental and theoretical approach. Experimental results demonstrated that this compound acts as a reliable corrosion inhibitor (η %) for mild steel in acidic environments, with its inhibition efficiency increasing as the inhibitor concentration rises. Adsorption behavior on the mild steel surface followed Langmuir and Temkin adsorption isotherms. Electrochemical polarization tests indicated that the compound exhibited a mixed corrosion type, and impedance spectroscopy revealed an increase in charge transfer resistance with higher inhibitor concentrations. Examination of the mild steel surface using SEM and Atomic Force Microscopy (AFM) confirmed the formation of a protective film. Wettability characteristics were assessed using the contact angle method. Frontier molecular orbital analysis revealed the HOMO and LUMO values for both the neutral and protonated forms of the compound. At 289 °C, the interaction energy for adsorption was found to be approximately −146.3006 kJ/mol for the neutral system and −135.8122 kJ/mol for the protonated system, while at 318 °C, the corresponding values were −140.6106 kJ/mol and −147.6022 kJ/mol. These findings collectively suggest the potential industrial utility of the investigated inhibitor as an effective corrosion inhibitor.

Ionenes as Potential Phase Change Materials with Self-Healing Behavior.

Ionenes are poly(ionic liquids) (PILs) comprising a polymer backbone with ionic groups along the structure. Ionenes as solid-solid phase change materials are a recent research field, and some studies have demonstrated their potential in thermal dissipation into electronic devices. Eight ionenes obtained through Menshutkin reactions were synthesized and characterized. The analysis of the thermal tests allowed understanding of how the thermal properties of the polymers depend on the aliphatic nature of the dihalogenated monomer and the carbon chain length. The TGA studies concluded that the ionenes were thermally stable with T10% above 420 °C. The DSC tests showed that the prepared ionenes presented solid-solid transitions, and no melting temperature was appreciated, which rules out the possibility of solid-liquid transitions. All ionenes were soluble in common polar aprotic solvents. The hydrophilicity of the synthesized ionenes was studied by the contact angle method, and their total surface energy was calculated. Self-healing behavior was preliminarily explored using a selected sample. Our studies show that the prepared ionenes exhibit properties that make them potential candidates for applications as solid-solid phase change materials.

Mechanism and Quantitative Characterization of Wettability on Shale Surfaces: An Experimental Study Based on Atomic Force Microscopy (AFM)

Wettability, as a vital tool for analyzing and describing oil flow, plays a significant role in determining oil/water relative permeability, residual oil distribution, and on–site recovery efficiency. Although the contact angle method is widely used for measuring wetting behavior, it is susceptible to the effects of surface roughness, oil–water saturation, and the distribution of mixed wetting within the range of droplet sizes. Additionally, millimeter–scale droplets fail to accurately represent the wetting distribution and the influencing factors at the micro/nano–scale. Therefore, this study presents a comprehensive investigation of the microstructure and wettability of shale samples. The characterization of the samples was performed using scanning electron microscopy (SEM) and atomic force microscopy (AFM) techniques to gain insights into their microscopic features, surface properties, and wettability. Results demonstrate the following: (1) Quartz and clay minerals tended to exhibit rough surface topography, appearing as darker areas (DA) under scanning electron microscopy (SEM). It is worth noting that plagioclase minerals exhibited brighter areas (BA) under SEM. (2) An increase in the content of minerals such as quartz and clay minerals was observed to decrease the surface oil wetting behavior. In contrast, plagioclase feldspar exhibited an opposite trend. (3) Based on the adhesive forces of the samples towards oil or water, a wetting index, I, was established to evaluate the wettability of shale at a microscale. The dimensionless contact angle W, obtained by normalizing the contact angle measurement, also consistently indicated oil wetting behavior. (4) By comparing the differences between I and W, it was observed that surface roughness significantly affected the behavior of water droplets. The presence of roughness impeded the contact between the solid and liquid phases, thus influencing the accuracy of the wetting results. Organic matter also plays a significant role in influencing surface wettability, and its distribution within the shale samples can lead to localized variations in wettability.