Changes In Wettability Research Articles

Experimental Investigation on the Interfacial Characteristics of Tight Oil Rocks Induced by Tuning Brine Chemistry.

Currently, research on enhancing imbibition oil recovery in tight oil reservoirs through the ion-tuning technique remains limited. Two critical parameters for capillary imbibition are the wettability and interfacial tension between oil and water. In this investigation, we manipulate the properties of two types of formation water for both aged and unaged samples by diluting brine and altering ion composition. Subsequently, we employ captive and pendant-drop methods to assess rock wettability and interfacial tension under varied brine conditions. Additionally, we elucidate the primary mechanisms underlying changes in rock wettability and interfacial tension. Meanwhile, we analyze capillarity characteristics and assess the relative significance of wettability and interfacial tension. Results indicate that there is a critical interfacial tension with progressive dilution of two types of formation water. However, modifying ion composition leads to a complex trend in interfacial tension, which can be explained qualitatively through the Gibbs adsorption isotherm. For unaged samples, the contact angle demonstrates a pronounced water-wet characteristic, showing a nonmonotonic trend with respect to dilution times. Remarkably, the rock surface exhibits the strongest water-wet, particularly evident in the case of FW-10, largely influenced by variations in interfacial tension. Conversely, aged samples demonstrate strong oil-wet, with a critical salinity resulting in the lowest contact angle, while altering brine ion types can alter rock wettability from strongly oil-wet to intermediate-wet, which is not sufficient to result in the wettability alteration. The removal of multivalent cations is proposed as the most effective method for wettability modification. Furthermore, capillarity variations among different brine cases are primarily contingent upon contact angle changes, and interfacial tension does not have a significant change when regulating the brine properties. Consequently, we emphasize the significance of wettability in the adoption of ion-tuned brine techniques for tight oil reservoirs. Overall, our study underscores the potential of reasonably regulating brine properties to enhance capillarity and, thereby, improve imbibition oil recovery.

Effects of surface wettability and density change during solidification of paraffin phase change materials

Phase change materials (PCMs) are widely used for thermal energy storage and other applications. During the solidification of a PCM, a volume change occurs due to thermal expansion and structural change of the molecules. A concave shape may be created during the solidification shrinkage. This paper investigates the shrinkage profile formed during the solidification of paraffin wax and its relationship with the surface wettability (contact angle), considering the effect of density changes. The contact angle of a paraffin droplet on a surface indicates the extent of adhesion between the solid surface and paraffin. The experimental study examines a mixture of wax with nanoparticles, wax with surfactants, different coatings on the container surface, and different solidification temperatures. Enhanced adhesion and increased shrinkage height are observed due to the non-polar interaction between coated surfaces and paraffin, facilitated by induced dipole-induced dipole forces. The addition of 3% octadecylamine enhances adhesion between paraffin and the container, as driven by dipole–dipole forces between the hydroxyl group on epoxy resin-container surfaces and the hydrophilic amine group of octadecylamine. The shrinkage height increases with a decrease in the contact angle of paraffin on the surface. The shrinkage profile also changes with the solidification temperature. The highest shrinkage profile is achieved for the highest solidification temperature.

Defect by design: Harnessing the “petal effect” for advanced hydrophobic surface applications

Hypothesis: In the interfacial wetting boundary, the superhydrophobic surface is often damaged, and the anisotropic wettability of its surface has attracted many researchers’ attention. The “petal effect” surface has typical anisotropic wettability. We predict that under the dual conditions of structural defects and high impact velocity, the “petal effect” becomes more adhesive on the surface.Experiments: This study refers to the droplet state on rose petals, structural defects were constructed on the superhydrophobic surface. This paper studies the influence of macro-structural defects on the wettability change from natural to bionic “lotus effect” to “petal effect” in both static and dynamic angles.Findings: Macro defects significantly change the static contact angle of the superhydrophobic surface. The higher the impact velocity of the droplet, the higher the energy dissipation of the “petal effect” surface (DSHS), which improves the adhesion of the surface to the droplet and prolongs the contact time. It is found that the defect structure and high impact velocity will directly affect the deposition and desorption of droplets on the superhydrophobic surface, and they are both essential. This wetting dynamic law is very likely to be helpful in the quantitative design of defect structure scale for dynamic desorption of droplets on superhydrophobic surfaces.

Experimental investigation of pool boiling performance on a coated copper surface using a two-step non-thermal plasma process

In this study, a stable hydrophilic thin layer resembling SiOx is formed on the copper surface by combining plasma polymerization using hexamethyldisiloxane (HMDSO) and Ar plasma activation. The effect of coating on the Heat Transfer Coefficient (HTC) and Critical Heat Flux (CHF) at two different subcooling temperatures is investigated through pool boiling experiments. It is found that the HTC and CHF of the modified surface improved by 42 % and 97 %, respectively. The chemical composition of the coating, as well as changes in surface roughness, wettability, and porosity, are studied using the Scanning Electron Microscope (SEM), Energy Dispersive X-ray spectrometer (EDX), Fourier Transform Infrared (FT-IR) spectroscopy, and contact angle measurement. The boiling/cooling experiments for the plasma-coated surface show good stability, demonstrating that the surface characteristics remain stable even after three boiling/cooling cycles.

Enhancing Injectivity in Lithuanian Hydrocarbon Reservoirs through Wettability-Altering Surfactant Injection

Improved and efficient recovery methods are investigated as possible candidates to arrest the production decline and to improve the injection capacity in hydrocarbon fields in Lithuania. The data show that the Cambrian reservoirs in Lithuania are mixed to oil-wet in nature, which results in poor water-flooding efficiency. Wettability alteration could help in improved water injection and, at the same time, it could help recover additional oil from the residual oil saturation zone of the reservoir. In this paper, a screening exercise is conducted to help alter reservoir wettability, improve water injection efficiency, and to improve oil recovery. Analytical and machine-learning supported methods are used for screening. Based on the screening results, dilute surfactant-based injection techniques are suggested as a potential method to improve injectivity and, thereby, recovery from the field. An initial experimental analysis targets the wettability of the rock from the field, followed by testing for wettability-altering surfactants. Based on the findings of the screening study and experimental analysis, it is recommended that we initiate a core flooding experimental program to investigate wettability changes and enhance injection and recovery from the field.

Relating Pore‐Scale Observations to Continuum‐Scale Models: Impact of Ganglion Dynamics on Flow Transport Kinetics

AbstractContinuum‐scale models used to model and predict two‐phase flow in the subsurface are often based on averaged flow parameters and do not consider pore‐scale fluid flow phenomena, for example, ganglion dynamics and thin‐film flow. As such, a major challenge in upscaling two‐phase flow for groundwater engineering applications is understanding the impact of disconnected flow and ganglion dynamics on continuum‐scale flow functions such as relative permeability‐saturation and capillary pressure‐saturation curves. In this study, we explored how changes in wettability and fluid velocity affect ganglion dynamics. We conducted pore‐scale numerical simulations with OpenFOAM to investigate the displacement of decane by water. Additionally, we examined how displaced phase saturation (a continuum‐scale flow function) responds to changes in dynamic fluid connectivity. We identified three different fluid flow regimes, that is, the connected pathway flow regime, ganglion dynamics (GD) flow regime, and droplet traffic flow regime, and studied the effects of changes in the wettability of the porous medium and the velocity of the invading fluid on the transitions between these different regimes. Our research showed that transitions between connected and disconnected pore‐scale flow regimes, which are induced by changes in fluid velocity and wettability, have a significant impact on both fluid displacement efficiency and average fluid flow transport kinetics.

Experimental Evaluation of CO2-Soluble Nonionic Surfactants for Wettability Alteration to Intermediate CO2-Oil Wet during Immiscible Gas Injection

Summary The change in wettability of limestone reservoirs from oil-wet toward gas-wet can enhance crude oil production during immiscible CO2 injection. Therefore, in this research, we investigated the impact of wettability alteration to CO2-wet on oil recovery factor via dissolution of fluorine-free, CO2-philic, nonionic surfactants such as C4(PO)6 and C41H83O19 in CO2. Based on the cloudpoint measurements, the dissolution pressures of nonionic surfactants in supercritical CO2 ranged between 2,100 psi and 2,700 psi (below the reservoir pressure, i.e., 3,000 psi) at reservoir temperature, 65°C; these pressures are commensurate with CO2-enhanced oil recovery (EOR) pressures. Also, the C4(PO)6 and C41H83O19 can reduce the CO2-oil interfacial tension (IFT). Moreover, the CO2/C4(PO)6 and C41H83O19 solutions can change the limestone wettability from strongly oil-wet (Θ ~ 20o) to intermediate CO2/oil-wet (Θ = 95o and 110o) at reservoir conditions. The relative permeability curves also confirmed it by changing the curvature to the left and decreasing the residual oil saturation in both cases of CO2/C4(PO)6 and C41H83O19 solutions. The 20.8% and 13.1% additional oil recoveries were achieved during the 30,000 ppm CO2/C4(PO)6 and C41H83O19 solution scenarios, respectively, relative to the pure CO2 injection scenario. These nonionic surfactants are not able to make CO2-in-oil foam; therefore, wettability alteration and perhaps IFT reduction are the dominant mechanisms of EOR induced by the dissolution of nonionic surfactants in CO2, instead of CO2 mobility control. Consequently, the dissolution of fluorine-free, oxygenated, CO2-philic, nonionic surfactants (such as C4(PO)6 and C41H83O19) in CO2 at 30,000 ppm concentration can be a well-qualified candidate for altering the limestone wettability to intermediate CO2-oil-wet during the immiscible CO2 injection.

Experimental investigation into coal wettability changes caused by reactions with scCO2-H2O

Geological CO2 sequestration (GCS) can help mitigate global warming and enhance methane recovery from coal beds. However, few studies have linked the effects of CO2 to surface chemistry changes controlling wetting behavior in deep coal beds. Contact angles (CAs) of CO2/N2-high volatile bituminous coal-water systems were measured under different temperatures and pressures. The surface chemistry and physical structure of coals were characterized to investigate changes in physicochemical properties and their relations with wettability after reactions. For N2 treatment, the time-dependence of static and dynamic CAs were insignificant, ranging within 4°. For gaseous CO2 treatment, the static CAs and the average advancing angles increased slightly. With supercritical (sc) CO2, both the static and dynamic CAs increased significantly, and θadv changed to intermediate-wet (92°). Reactions with minerals exposed to scCO2 resulted in greater surface roughness and heterogeneity, greater contact angle hysteresis and more surface sites occupied by scCO2 rather than H2O. Increases in hydrophobic functional groups and decreases in hydrophilicity were shown by FTIR spectra, reflecting the shedding of polar oxygen-containing functional groups, reduction of hydrogen bonds, and increasing percentage of hydrocarbons. XRD patterns obtained following scCO2-treatment showed that crystallite growth and molecular polymerization were higher toward graphite-like. The calculated structural parameters of functional groups and crystallites both showed elevated coal rank. Changes in crystallite structure, notably higher carbon content and decreased negative surface charge, are unfavorable for water-wetting. This study contributes to understanding surface chemistry changes responsible for decreased wettability during CO2-enhanced coal bed methane recovery and GCS in coal reservoirs.

Static and impact performance of engineered cementitious composites with hybrid graphite nano platelets modified PVA and shape memory alloy fibres

Polyvinyl alcohol (PVA) fibre has been widely adopted to produce engineered cementitious composites (ECC), the overall performance of which is highly dependent on the fibre surface characteristics. The traditional approach to improve PVA fibre bridging ability is to tailor the surrounding matrix properties. However, this common practice need to do a lot of laborious experimental works, and thus it has limited efficiency and practicality. Therefore, special surface treatments on PVA fibres are required to create synergistic interactions between fibre and surrounding matrix to retain excellent tensile ductility and better mechanical performance. This paper proposes a novel treatment method for PVA fibres using nano graphite platelets to modify the PVA fibre surface and improve the mechanical properties of PVA fibre reinforced ECC. To evaluate the effectiveness of such treatment, a systematic experimental study was performed. Firstly, static contact angle measurements, scanning electron microscopy and atomic force microscopy were employed to monitor the wettability and physical changes on the fibre surface. Then, the static and dynamic mechanical properties as well as microstructural characteristics of ECC with hybrid modified PVA fibres (2 vol%) and shape memory alloy (SMA) fibres (0.25 vol%, 0.50 vol% and 1 vol%) were examined. The results indicate that the graphite nanoplatelets treated PVA fibres (GPVA) exhibit high hydrophobicity and surface roughness providing steady-state crack propagation, which is a necessary condition to ensure multiple cracking and improving the higher fibre bridging complementary energy. This is evidenced by significantly densified the transition zone between the graphite treated PVA fibres and the matrix, and improved the flexural tensile strength and the toughness. The calculated surface roughness of 28.86 μm and lots of peaks and valleys on the 3D topographical micrographs of the cracking faces confirmed that 1 SMA-2 GPVA specimen efficiently participated in transferring stress through the composite, leading to a greater vertical impact reaction force. Finally, the structure-property relation for flexural versus fracture behaviour and the effectiveness of SMA fibres on the crack-healing feature of the composites were studied by using digitized fractal analysis and through the heat treatment. The disseminated fracture energy (Ws/Gf) value reached 130 and the crack sizes the crack size decreased by 34 %, which were much better than that of the reference composites. The nano treatment of PVA fibres in ECC provides an innovative and sustainable solution for engineering structures with requirement of high tensile ductility and high impact resistance, e.g., military infrastructure and industrial floors.

Materials Characterization of Stereolithography 3D Printed Polymer to Develop a Self-Driven Microfluidic Device for Bioanalytical Applications.

Stereolithography (SLA) 3D printing is a rapid prototyping technique and reproducible manufacturing platform, which makes it a useful tool to develop advanced microfluidic devices for bioanalytical applications. However, limited information exists regarding the physical, chemical, and biological properties of the photocured polymers printed with SLA. This study demonstrates the characterization of a commercially available SLA 3D printed polymer to evaluate the potential presence of any time-dependent changes in material properties that may affect its ability to produce functional, capillary-action microfluidic devices. The printed polymer was analyzed with Fourier transform infrared-attenuated total reflectance, contact angle measurements, tensile test, impact test, scanning electron microscopy, and fluid flow analysis. Polymer biocompatibility was assessed with propidium iodide flow cytometry and an MTT assay for cell viability. The material characterization and biocompatibility results were then implemented to design and fabricate a self-driven capillary action microfluidic device for future use as a bioanalytical assay. This study demonstrates temporally stable mechanical properties and biocompatibility of the SLA polymer. However, surface characterization through contact angle measurements shows the polymer's wettability changes over time which indicates there is a limited postprinting period when the polymer can be used for capillary-based fluid flow. Overall, this study demonstrates the feasibility of implementing SLA as a high-throughput manufacturing method for capillary action microfluidic devices.

Interfacial tension and wettability alteration during hydrogen and carbon dioxide storage in depleted gas reservoirs

The storage of CO2 and hydrogen within depleted gas and oil reservoirs holds immense potential for mitigating greenhouse gas emissions and advancing renewable energy initiatives. However, achieving effective storage necessitates a thorough comprehension of the dynamic interplay between interfacial tension and wettability alteration under varying conditions. This comprehensive review investigates the multifaceted influence of several critical parameters on the alterations of IFT and wettability during the injection and storage of CO2 and hydrogen. Through a meticulous analysis of pressure, temperature, treatment duration, pH levels, the presence of nanoparticles, organic acids, anionic surfactants, and rock characteristics, this review elucidates the intricate mechanisms governing the changes in IFT and wettability within reservoir environments. By synthesizing recent experimental and theoretical advancements, this review aims to provide a holistic understanding of the processes underlying IFT and wettability alteration, thereby facilitating the optimization of storage efficiency and the long-term viability of depleted reservoirs as carbon capture and storage or hydrogen storage solutions. The insights gleaned from this analysis offer invaluable guidance for researchers, engineers, and policymakers engaged in harnessing the potential of depleted reservoirs for sustainable energy solutions and environmental conservation. This synthesis of knowledge serves as a foundational resource for future research endeavors aimed at enhancing the efficacy and reliability of CO2 and hydrogen storage in depleted reservoirs.

Modified ceramic membrane with temperature responsiveness and self-cleaning property for efficient separation and catalysis

Composite membrane that integrating catalytic degradation with membrane separation offers a promising solution for one-step treatment of complex wastewater. However, the challenge of membrane fouling by multi-component pollutants, impedes their broader applications. Herein, building on previous work, temperature responsive polymers are grafted onto a nano-Ag decorated ceramic substrate for enhanced dye removal and anti-fouling property. The grafting process is optimized in terms of reaction temperature (75 ℃), reaction time (4 h), and monomer concentration (VMDMO: 0.01 M, MATE: 0.02 M, DMAEMA: 0.04 M). The morphology of the membrane surface after each modification step is characterized by FESEM. The prepared composite membrane manifests temperature-responsive property. As the temperature rises from 20 °C to 85 °C, the pure water flux of the membrane increases from 68.8 L m-2h−1 to 434.4 L m-2h−1 (0.1 MPa), reflecting a six-fold enhancement. And this temperature response is reversible. In oil-in-dye containing water treatment, the composite membranes demonstrate an oil separation efficiency exceeding 98.0 % and a dye degradation efficiency surpassing 99.0 %. By elevating the ambient temperature, the flux recovery of the composite membrane is 91.2 %, which is much higher than that of the original membrane (58.8 %). This is ascribed to the physical configuration and wettability changes of the grafted polymers at different temperature, which facilitate the release of foulants. This study introduces a novel strategy (surface modification with temperature responsive polymer) for preparing anti-fouling ceramic composite membrane with the function of catalytic degradation of dyes. It would have potential applications in environmental remediation.

Different effects of resins and asphaltenes concentration of crude oil on sandstone wettability

The influence of asphaltenes in crude oil on sandstone wettability is widely acknowledged. Although asphaltenes are recognized for their stronger polarity compared to resins, resins also contain the similar acidic and nitrogen-containing compounds to those found in asphaltenes. Nevertheless, the impact of resin adsorption on altering sandstone wettability, the different effects of vary concentrations of resins and asphaltenes, and their microscopic mechanisms influencing sandstone surfaces remain ambiguous. Thus, in this study, resins and asphaltenes were isolated from crude oil individually to investigate the different effects of their concentrations on sandstone wettability and the specific reasons. The contact angle measurements, atomic force microscopy (AFM), energy dispersive spectroscopy (EDS), and Cryo-environmental scanning electron microscopy (ESEM) were used to examine and explain the wettability changes of Berea sandstone slices before and after exposure to varying concentrations kerosene solutions of resins and asphaltenes. The results reveal that sandstone wettability could not be changed from strongly water-wet to oil-wet, even at resin concentrations as high as 50.0 mg/mL kerosene. In contrast, lower concentrations of asphaltenes, equivalent to a 5.0 mg/mL kerosene threshold, can facilitate the wettability transition process. After the adsorption of resins and asphaltenes, the roughness of the clay surface changes much more significantly than that of the quartz surface. Combined with the observation of ESEM and the results of EDS, it is believed that the resins and asphaltenes preferentially adsorb to clay surfaces, especially chlorite, rather than quartz surfaces. Clay could provide favorable sites for the accumulation of oxygen-containing compounds, leading to enduring clay-organic complexes that serve as anchor molecules for the adsorption of other compounds, ultimately causing the sandstone surface to an oil-wet state. These results may provide theoretical support for better core aging process in the laboratory, surfactant development and enhanced oil recovery procedure optimization in the oilfield.

Polymer System Based on Polyethylene Glycol and TFE Telomers for Producing Films with Switchable Wettability.

Today a lot of attention is paid to the formation of thermosensitive systems for biomedical and industrial applications. The development of new methods for synthesis of such systems is a dynamically developing direction in chemistry and materials science. In this regard, this paper presents results of the studies of a new synthesized supramolecular polymer system based on polyethylene glycol and tetrafluoroethylene telomers. The films formed from the polymer substance have the property of switching wettability depending on temperature after heating activation. It has been established that the wettability changes at 60 °C. The contact angle of activated hydrophobic polymer film reaches 143°. Additionally, the system exhibits its properties regardless of the pH of the environment. Based on data obtained by the methods of infrared and x-ray photoelectron spectroscopy, differential thermal analysis and thermal analysis in conjunction with wettability and morphology, a model of the behavior of molecules in a polymer system was built that ensures switching of the hydrophilic/hydrophobic surface state. The resulting polymer system, as well as films based on it, can be used in targeted drug delivery, implantation surgery, as sensors, etc.

Evolution of shale wetting properties under long-term CO2/brine/shale interaction: Implications for CO2 storage in shale reservoirs

In the case of Carbon Geological Storage (CGS), the wettability is one of the main parameters controlling the CO2 injection capacity and CO2 plume movement, which affects the safety of long-term CO2 storage. A full evaluation of this parameter is essential for risk evaluation and storage capacity estimation. The objective of this study was to investigate the wettability changes of shales from the Chang 7 Formation in the Ordos Basin by exposing the samples to ScCO2/brine for 10/20/30/and 60 days. The mineral composition, pore structure, chemical functional groups, and surface morphology changes of the shale were analyzed using x-ray diffractometer (XRD), low-temperature nitrogen adsorption (LN-N2), infrared spectroscopy (FTIR), and scanning electron microscopy (SEM). In addition, the solid-drop method was used to measure the contact angle of shale samples at different times of ScCO2 soaking. The results show that after 60 days of continuous ScCO2 soaking, the shale water contact angle and chemical group peak spectrum generally show an increasing trend, which is caused by the reduction of carbonate and clay mineral content. The prolonged time of ScCO2 soaking weakens the shale's water wettability and reduces the water-locking effect (water has a sealing effect in the pore channel of the reservoir), capillary force, and the height of CO2 sequestration columns, which is favorable for shale gas extraction (a method of extracting natural gas from shale rock by CO2 fracturing), but it may increase the CO2 geological leakage risk. The results have important implications for regulating the change of shale water wettability, and this study can also better provide theoretical references for Carbon Geological Storage programs.

Photo‐Arbuzov Reactions as a Broadly Applicable Surface Modification Strategy

AbstractChemical vapor deposition (CVD) polymerization is a commonly used approach in surface chemistry, providing a substrate‐independent platform for bioactive surface functionalization strategies. This work investigates the Arbuzov reaction of halogenated polymer coatings readily available via CVD polymerization, using poly(4‐chloro‐para‐xylylene) (Parylene C) as a model substance. Postpolymerization modification of these coatings via catalyst‐free and UV‐induced Arbuzov reaction using phosphites results in phosphonate‐functionalized polymers. The combination of infrared reflection‐absorption spectroscopy (IRRAS), X‐ray photoelectron spectroscopy (XPS), and time‐of‐flight secondary ion mass spectrometry (ToF‐SIMS) provides detailed insights into the reaction progress. Time‐dependent studies suggest that the non‐polar phosphites penetrate deep into the CVD films and react with the polymer film. In addition, ToF‐SIMS, scanning electron microscopy (SEM), and atomic force microscopy (AFM) confirm spatial control of the reaction, resulting in localized chemical and topographical surface modification, recognizable by changes in interference color, fluorescence, and wettability. Preliminary 3D fluorescence spectroscopy investigations indicate tunable near‐infrared emission of these polymer films. This work is the first step toward generating multifunctional polymer coatings based on chemically modifiable, CVD polymers with potential applications in biomaterials, sensors, or optoelectronics.

Study on the Wettability and Methane Desorption Characteristics of Coal under High Pressure with Different Surfactants.

In the process of coalbed methane extraction, due to the strong hydrophilicity of coal, the surface interaction force between water and the coal matrix is strong. The hydrophobic effect of the coal seam during drainage and pressure reduction is not significant, and adsorbed methane is difficult to desorb. In order to reduce the surface interaction force promoting methane desorption between water and coal, the surfactants NH766, G526, and D001 with a concentration of 0.1% were selected. A pressure of 12 MPa, which is close to that used for the on-site mining of coalbed methane in Baode, was selected as the experimental condition to simulate hydraulic fracturing of high fat coal, and the influence of different surfactants on methane desorption characteristics was analyzed. Combining contact angle experiments and infrared spectroscopy experiments, we explored the changes in wettability of the coal samples. We compared the changes in wettability and methane desorption characteristics and explored the similarities between these changes. The experimental results showed that after NH766 treatment, the content of oxygen-containing functional groups in coal rock decreased by 30%, and the contact angle of the coal matrix surface increased by 10°. Furthermore, its hydrophobicity was enhanced, and the desorption amount increased by 24%. In contrast, the oxygen-containing functional groups in coal rock after G526 and D001 treatments increased by 5% and 16%, respectively, and the contact angle of the coal matrix surface became smaller. Furthermore, its hydrophilicity was enhanced, and the desorption amount was reduced by 12.5% and 20%, respectively. NH766 reduces wettability and promotes methane desorption, and it can be applied to improve CBM extraction efficiency. G526 and D001 enhance wettability and inhibit methane desorption, which make them suitable for dust prevention and gas control in coal mines.

Smart antibiofouling composite coatings based on photothermally-active polyaniline and thermo-responsive poly(N-isopropylacrylamide)

Marine biofouling profoundly affects the economic viability of the marine sector. With a view towards addressing this issue, this work reported the successful development of smart photo-responsive and thermo-responsive antibiofouling coatings by combining photothermally-active polyaniline (PANI) with temperature-sensitive poly(N-isopropylacrylamide) (PNIPAM). Under light irradiation, the PNIPAM/PANI coating could be photothermally heated to temperatures as high as 89.3 ± 1.6 °C, delivering a maximum antibacterial rate of 99.99 %. Impressively, light-induced temperature changes in the PNIPAM/PANI coating caused dynamic changes in film morphology and wettability. Upon lowering the temperature to below the lower critical solution temperature (LCST) of PNIPAM, the water contact angle of the PNIPAM/PANI coating decreased from 81° to 35° and the coating surface roughened appreciably, resulting in a 99.99 % release rate for both E.coli and S. aureus, thus achieving a dynamic self-cleaning effect. Furthermore, the developed PNIPAM/PANI coating demonstrated excellent resistance against protein and algae adhesion. These findings showcase the broad application potential of PNIPAM/PANI antifouling coatings in the marine sector.

Polycaprolactone-Based Composite Electrospun Nanofibers as Hybrid Biomaterial Systems Containing Hydroxyl- or Carboxylic Acid-Functionalized Multiwall Carbon Nanotubes

Composite electrospun nanofibers based on polycaprolactone (PCL) have shown promise in various biomedical applications due to their unique properties. This study investigates the effects of incorporating hydroxyl (–OH)- or carboxylic acid (–COOH)-functionalized multiwall carbon nanotubes (MWCNTs) into PCL matrices. Two types of functionalized additives, MWCNT-OH and MWCNT-COOH, were used at different concentrations (0.06 and 0.12 wt%). Various characterization techniques including FTIR, XRD, AFM, SEM, water contact angle analysis, and tensile strength testing were employed to evaluate changes in nanofiber morphology, crystallinity, surface topography, wettability, and mechanical properties. In addition, in vitro cytotoxicity assays were conducted using HUVECs and L929 fibroblasts over 1-, 3-, and 5-day intervals. This study represents a novel examination of (–OH)- and (–COOH)-functionalized MWCNTs as additives in electrospun PCL biopolymer matrices. The findings indicate that incorporating small amounts of (–OH)- or (–COOH)-functionalized MWCNTs enhances the physicochemical characteristics of PCL nanofibers, making them more suitable for biomedical applications. While both types of functionalized MWCNT additives improved properties compared to pure PCL nanofibers, (–COOH)-functionalized MWCNT-incorporated nanofibers exhibited the most favorable features. In conclusion, this research highlights the potential of tailored PCL-based composite nanofibers containing functionalized MWCNTs as advanced biomaterial systems for biomedical applications, contributing to the development of innovative biomaterials for diverse biomedical contexts.

Influence of surfactant adsorption on coal oxidation and wettability: Experimental discussion and model development

To further investigate the physicochemical properties and wettability changes of surfactant-modified coal after oxidation, the contact angle, industrial composition, and functional groups of the surfactant-modified coal were measured. The experimental data were analyzed using a ridge regression prediction model to explore the relationship between the physicochemical properties and the wettability. The results indicate that the oxidated-modified coal has a worse wettability at room temperature. The adsorption of SL and CDEA surfactants effectively impedes the increase in the contact angle of the oxidized coal. The hydrophilic functional group (2#CO, C–O–C, RHCCH2) in coal demonstrates higher sensitivity to surfactants, while the hydrophobic functional group (2# Free OH, 1#CC) exhibits greater reactivity. There is a strong correlation between the industrial composition, structural parameters, and the contact angle. The quantitative influence of the parameters on the contact angle is as follows: FCad > Vad > P1 ≥ P4 ≥ Mad ≥ P3 ≥ P2. A coal wetting model is established that considers the combined action of surfactants and coal quality. These findings suggest that wettability is determined by multiple parameters, providing a basis for discovering new reagents that significantly enhance coal wettability and reduce coal oxidation activity.