Reduction Of Surface Energy Research Articles

One-step development of photothermal omniphobic membrane for vacuum membrane distillation towards sustainable water desalination using solar energy

Nowadays, development of photothermal omniphobic membranes (POMs) for water desalination using solar energy has gained considerable attention to face water and energy challenges in a sustainable way. Scientists have been developing POM via different techniques based on photothermal component loading and surface energy reduction, all of which suffer from multi-step processes. Obviously, researchers and especially industrial developers aspire to one-step techniques that make the production process highly accelerated and economical. In this study, a one-step technique to develop POMs is demonstrate, using which the omniphobic and photothermal properties are simultaneously imparted to the membrane through being integrated with the membrane fabrication process. The technique works based on elaborate design of membrane surface chemistry and roughness via electrospinning of poly(vinylidene fluoride) (PVDF)/poly(1H,1H,2H,2H-perfluorooctyl acrylate) (PPFOA) blend solution containing carbon black nanoparticles (CB NPs). Optimum concentrations for PPFOA and CB NPs with respect to the PVDF weight were obtained as 60 and 15 wt%, respectively. The developed membrane exhibited permeate flux and salt rejection as high as 2.94 kg/m2·h and > 98 %, respectively, under one sun radiation. Evaporation rate and efficiency of the developed membrane were calculated as 1.49 kg/m2.h and 83.5 %, respectively. The membrane exhibited stable long-term performance for 600 min in contact with the sodium dodecyl sulfate (0.8 mM)-containing NaCl aqueous solution (3.5 wt%). Besides single-step implementation, the introduced technique benefits from endowing the entire membrane structure with omniphobic and photothermal properties not only the membrane surface. This can drastically improve the membrane performance and life time.

Durable Organic Coating-Free Superhydrophobic Metal Surface by Paracrystalline State Formation.

The chemical instability of traditional organically-decorated superhydrophobic metal surfaces is a significant issue, severely limiting practical applications. This is due to the susceptibility of low surface energy coatings to ion permeation, decomposition, and exfoliation, especially in harsh environments. Here, organic coating-free, durable superhydrophobic surfaces on Al alloys by developing the paracrystalline state of a bionic anthill tribe structure is successfully achieved, using femtosecond laser element-doping microstructuring followed by repetitive annealing processes. Remarkably, the inherent superhydrophobic properties of the sample are maintained for ≈2000 h in a corrosive 3.5 wt.% NaCl aqueous solution, significantly surpassing the performance of traditional organic coatings. Moreover, this inherent superhydrophobicity remains nearly unchanged, even after rigorous electrochemical reaction measurements. Additional tests involving UV irradiation (>100 h), freezing cycles (>100 cycles), and acid/alkali resistance (>65 h) further demonstrate that the environmental adaptability of the surface far exceeds that of silane-coated surfaces. Ab initio calculations reveal that the formation of the paracrystalline state reduces surface energy and enhances chemical stability, thereby extending the durability of the superhydrophobic metal. These findings offer a powerful strategy for utilizing atomic-level structural rearrangements to design inherent superhydrophobic surfaces without the need for organic coatings.

Water-induced surface ordering facilitating the microcutting of ductile metals

Metal cutting is a crucial process in modern manufacturing. Enhancing the machinability of metals can significantly improve their production efficiency and surface integrity. Coating surface-active media (SAM) on the free surface of the metals before cutting is an easy method to improve machinability, which usually pertains to the category of the renowned Rehbinder effect. However, the existing SAM is usually hazardous and complex materials. Besides, the effect of SAM on the local structure of the metal surface remains unclear. In this study, water is employed as a simple yet often overlooked SAM in the microcutting of copper. Using water as SAM also allows the employment of X-ray absorption fine structure spectroscopy (XAFS) to study the local structure of copper with and without water coating. Results show that water coating on the free surface of copper can significantly reduce the cutting force and chip thickness, and improve the surface finish. Interestingly, removing the water coating enables the recovery of the cutting force, demonstrating a reversible effect. Based on the XAFS results and molecular dynamics simulation, a water-induced surface ordering mechanism is proposed to explain the findings from the microcutting experiments. This mechanism suggests that water molecules can induce surface ordering in copper, resulting in reduced surface energy and fracture toughness of copper, thus enhancing machinability. This work provides valuable insights into the comprehension of the Rehbinder effect and shows that picometer-scale modifications of the surface atom arrangement can considerably alter the deformation mode of metals, paving the way for the development of new manufacturing processes.

Enhanced Thermodynamic Stability of Delithiated Nano-LiCoO2 by Lanthanum Doping.

The dynamic environment within lithium-ion batteries induces significant changes in local thermodynamic functions, hampering the accurate prediction of the stability of the cathodes during cycling. While delithiation primarily affects the surface properties of the cathode structure, there is a lack of fundamental understanding concerning the evolution of interfacial energies with varying stoichiometry. Here, we used microcalorimetry to quantify the thermodynamic changes between the stoichiometric and partially delithiated nano-LiCoO2 states for the first time. A mild delithiation from LiCoO2 to Li0.71CoO2 caused a surface energy reduction, negatively affecting the adhesion between adjacent grains by ∼0.4J/m2. The introduction of lanthanum at 1.0 atom % reduced the surface energy of the stoichiometric LiCoO2 while forcing a constant surface energy state during delithiation down to Li0.57CoO2. This reduced the thermodynamic stress between grains during lithium cycling, mitigating degradation mechanisms. The lanthanum-induced surface stabilization also inhibited the coarsening and dissolution of the cathode particles. We used electron microscopy to propose an atomistic mechanism by which the lanthanum doping pins surface dissolution for improved cathode stability.

Thermal decomposition temperature-dependent bonding performance of Ag nanostructures derived from metal–organic decomposition

In wide-bandgap semiconductor power device packaging, die bonding refers to attaching the die to substrate. Thereby, the process temperature of Ag sintering for the die bonding should be low to prevent damage to fragile dies. Herein, an organic-free strategy using Ag nanostructures derived from the thermal decomposition of metal–organic decomposition (MOD) was proposed to achieve low-temperature bonding. Significant effects on bonding performance were determined by the thermal decomposition temperature, which in turn determined the organic content and sintering degree of Ag nanostructures. At a low thermal decomposition temperature of 160 °C, incomplete decomposition resulted in high organic content in the Ag nanostructures, causing large pores inside the Ag joints owing to the generation of gaseous products. Owing to the Ag particles with naked surfaces and wide size distribution, the Ag nanostructure obtained at 180 °C showed an excellent bonding performance, resulting in a high shear strength of 31.1 MPa at a low bonding temperature of 160 °C. As the thermal decomposition temperature was 200 °C, sintering among Ag particles increased the particle size, resulting in a reduction of surface energy and driving force for sintering. We think that uncovering this underlying mechanism responsible for the bonding performance will promote the application of Ag MOD in the die bonding of WBG power devices.Graphical abstract

Impregnate Carbonation: CO2-Guided In Situ Growth of Robust Superhydrophobic Structures on Concrete Surfaces.

Superhydrophobic surfaces applying on concrete can greatly improve the durability of concrete by preventing the damage from water. However, traditional design of superhydrophobic concrete surfaces by external coating encounters to problems of flaking and poor surface robustness, while that by adding hydrophobic agents or particles faces the challenges of strength damage of concrete. Drawing inspiration from the carbonation phenomenon of concrete, here a new design of in situ growing superhydrophobic structures on concrete is proposed: The concrete sample is impregnated into Mg2+-containing silane-water system with continuous CO2 injection. The contact angle of the concrete surface achieves 171.9° without obvious strength decrease after 120 min, which are mainly attributed to the formation of CaxMg1-xCO3 crystals with micro-nano-structures and the reduction of carbonates surface energy by silane. This superhydrophobic concrete structure can be divided into a superhydrophobic-hydrophobic-hydrophilic three layers structure, providing the stable water-proof protection under mechanical fatigue, capillary water absorption, UV aging, sulfate attack, and impurity water impact tests due to the in situ growing robust superhydrophobic structures. Furthermore, it captures 29.80gm-2 CO2 during the reaction process, providing new insights for the design and preparation of eco-friendly superhydrophobic concrete.

Hierarchy-constructed superhydrophobic and transparent coating modified intraocular lens by layer-by-layer self-assembly for glistening reduction and antiadhesion

Intraocular lens (IOL) implantation surgery is the most effective treatment for cataract. However, glistening formed by the incoming liquid microvacuoles can significantly damage postoperative visual quality after prolonged implantation, for which there is still lack of effective clinical treatment. In this study, inspired by the amazing water-repellency of natural superhydrophobic surface, a functionalized IOL material modified with the superhydrophobic and transparent coating was prepared using layer-by-layer electrostatic self-assembly technique combined with fluorination. After the alternate deposition of multiple cationic/anionic polyelectrolytes and silica nanoparticles of varying sizes on IOL materials, the constructed multilayered films with special surface roughness were further fluorinated to reduce surface energy. In addition to its excellent superhydrophobicity and transparency, this multilayered coating could efficiently eliminate the glistening formation of IOL under accelerated condition in vitro. Furthermore, the in vitro experiments with water droplets, cells, and bacteria suggested the superior antiadhesion property of such coating modified materials. The biocompatibility evaluation, both in vitro and in vivo, demonstrated the great biocompatibility of the materials modified with superhydrophobic and transparent coating. Therefore, this multilayered coating with excellent superhydrophobic and transparent characteristics can provide an available approach aiming at anti-glistening and antiadhesion of IOL materials. Advances in the fabrication process of surface coating with specific functions will enhance the practical application and clinical success of modified IOLs.

An integrated approach for developing a durable and superhydrophobic anti-corrosion coating inspired by biomimetic starfish surface structures

Applying superhydrophobic coatings with excellent anti-corrosion, anti-fouling, self-cleaning, antibacterial, and wear-resistant properties is a promising approach to protect metal surfaces. This study presents a novel and cost-effective approach, inspired by the biomimetic structure of starfish, to develop a durable and superhydrophobic coating. Unlike traditional methods, we introduce a meticulously engineered tetrapodal ZnO@SiO2-fluorosilane composite that forms a unique hierarchical micro-nano core-shell structure, reducing surface energy and exceptional performance. The formulation combines perfluorooctyl triethoxysilane (FOTS)-modified SiO2, silicone polyester, and tetrapodal ZnO (T-ZnO) in thermoplastic polyurethane (TPU), resulting in a first-of-its-kind T-ZnO@SiO2-FOTS (ZSF) coating with superhydrophobic properties, demonstrated by a water contact angle of 160°, a sliding angle of 3°, and the lowest surface free energy of 14.50 mN/m, contributing to excellent anti-corrosion properties (corrosion rate of 1.44 × 10−6 mm/year) and a corrosion inhibition efficiency of 99.87 %. In addition, the coating exhibits remarkable mechanical durability, adhesion enhancement, and stability against harsh environmental agents, including salt spray, HCl, and NaOH. Our biomimetic approach leverages the starfish-inspired surface design and highly crosslinked interface to enhance resilience, making this coating more robust under real-world conditions. These results provide a promising pathway for the development of multifunctional coating materials suitable for various solid surfaces.

Effect of laser speed on neck formation in SS316L powder joining for LPBF

The objective of this study is to comprehend how changes in laser speed affect the behaviour and features of neck formation in SS316L during powder bed fusion. This study examines the impact of various laser speeds on the neck formation in the commonly used SS316L. Uniweld Laser 3000 was used for laser joining. A constant laser power of 15 W and laser scan speed of 25–150 mm/s were implemented, and powder joining within a single track was observed. Results show that neck size decreases with increasing laser scanning speed and no particle joining occurs at 150 mm/s scan speed, as it is considered too fast for sufficient heat absorption and melting. As laser speed decreases to 125 mm/s, neck starts to form because the particles absorb more heat, which facilitates melting and bonding. Surface diffusion occurs early at this stage because it requires only a small amount of energy to break atomic bonds on the surfaces of particles compared to those in the internal part. This process involves atoms moving along the surfaces of the particles, facilitating the initial stages of sintering by reducing surface energy and causing neck formation between particles. At 125 mm/s, the particle shape remains spherical, and the average neck size is 49 μm. At 100 μm, the powder average neck size is 62 μm. Moreover, the powder completely merges at 50 mm/s and 25 mm/s. The neck formed between particles considerably improves the product's mechanical strength by strengthening bonds between particles. Material density increases with neck quality, and stable neck growth can reduce the porosity of the final parts. Ensuring thermal stability in the laser powder bed fusion allows consistent heat to particles, ensuring even temperature in materials and ultimately facilitating stable neck growth. Thermal stability enables atoms in particles to migrate efficiently and prevents defects, such as bubbling, which increases porosity in printed parts. Therefore, a slow scanning speed allows particles to absorb more heat for melting, increasing the neck size of particles. This knowledge is useful for optimizing laser processing parameters in various industrial applications.

The effect of surface treatments on the bond strength of polyetheretherketone posts: a systematic review protocol

Abstract* Background Polyetheretherketone (PEEK) is widely used in the biomedical field due to its outstanding biological and mechanical properties. Originally employed as a temporary abutment in implantology, recent research has expanded its indications for more definitive applications, such as frameworks and dental post and core. This shift requires a thorough assessment of PEEK’s adhesion and mechanical characteristics. However, PEEK’s inert properties and intricate chemistry create difficulties in surface treatment, resulting in reduced surface energy and inadequate adhesion. Inducing specific physical and chemical changes aims to overcome these challenges and enhance adhesion for PEEK. Despite its numerous clinical trials, standardized protocols remain lacking. This systematic review aims to assess the impact of surface treatments on the bonding performance of PEEK posts. Methods A detailed search of the literature will be conducted across several databases including PubMed, Scopus and clinical trial registries. Additional databases such as Cochrane Central, EMBASE, Web of Science and EBSCO will also be included. The search strategy will target controlled randomized studies and non-randomized clinical trials evaluating the impact of surface treatments on PEEK post adhesion strength. The Newcastle-Ottawa Scale (NOS) will be used to assess bias in non-randomized studies, while the Cochrane Risk of Bias (ROB II) tool will be employed for evaluating randomized controlled trials. Data extraction will focus on study design, treatment methods, outcomes and results. This systematic review protocol will adhere to the guidelines for systematic reviews outlined in the Preferred Reporting Items for Systematic Reviews and Meta-Analyses (PRISMA). Discussion The discussion will explore the implications of findings on clinical practice, highlighting the importance of enhancing PEEK’s bioactivity and surface energy to improve bonding efficacy in dental procedures. Moreover, it will suggest areas for future research to advance dental materials science, aiming to optimize the utilization of PEEK in dental applications Systematic review registration PROSPERO: CRD42024529783 (Registered on 08/04/2024).

Functionalized flattened bamboo board: In-situ immersion assembly of flame-retardant, waterproof and anti-mold composite coatings

The flattened bamboo board (FB) represents a promising innovation in the bamboo industry. To address the challenges of flammability and hygroscopicity, composite coatings consisting of melamine (MEL), phytic acid (PA), cerium ions (Ce3+), and sodium laurate (La) are assembled on the FB surface through an in-situ impregnation strategy. The resulting MEL/PA-Ce3+@La FB exhibits exceptional flame retardancy. It achieves a V-0 rating in the vertical burning test (UL-94) and boasts a high limiting oxygen index (LOI) value of 38.5 %. The coated FB exhibits superhydrophobicity, evidenced by a water contact angle of 156.5°, which can be attributed to the in-situ growth of PA-Ce3+ complexes (for constructing micro/nanoscale coarse structures) and the modification with La (for reducing surface energy).This superhydrophobic surface imparts both self-cleaning and anti-mold properties to the coated FB. Moreover, the coated FB exhibits excellent mechanical stability, withstanding 36 cycles of sandpaper abrasion and tape peeling without losing its hydrophobicity. In summary, this work provides an innovative strategy for the bamboo processing industry to produce flattened bamboo boards with combined flame retardancy, superhydrophobic and anti-mold properties. Such versatility holds significant potential to facilitate the utilization of flattened bamboo boards in the construction and decorative materials industries.

Water-resistant properties improvement of aluminium oxide nanoparticles treated kraft paper by sparking process

This study aims to improve the hydrophobicity of non-sizing Kraft paper (KP) surfaces using nanoparticle coating through the sparking process. The aluminium oxide nanoparticles (Al2O3 NPs) were used for surface modification on KP through the sparking process, optimizing with varying sparking cycles (5–20 times), annealing temperatures (60–120 °C), and annealing times (1–3 h). Then, the Al2O3 NPs treated KP were examined by XRD, FT–IR, SEM, EDX, and AFM, respectively. The water contact angle (CA) was used to examine the water-resistant properties of the treated KP. The treated KP with varying sparking cycles up to 15 times showed higher surface coverage and enhanced fine roughness surface on the treated KP. The fine roughness surface of KP induced hydrophobicity (126° of CA) on the surface of KP at 15 sparking cycles. Similarly, the higher CA for hydrophobicity surface on treated KP from varying temperatures and times of the annealing process was demonstrated at 120° for 3 h. Therefore, the treated KP with 15 times of sparking cycle, annealing temperature at 120 °C for 3 h was defined as the optimized condition in this work. Furthermore, the developments of hydrophobicity and superhydrophobicity on the treated KP with CA at 135 and 155° were observed for the non-sizing and sizing KP, respectively. This indicated that the increased surface roughness and reduced surface energy of the treated KP simultaneously delayed the water absorption times on the KP surface. Consequently, the nano-treating of Al2O3 NPs using the sparking process shows the promising feature of inducing superhydrophobicity on the KP surface, which can produce a water-repellent corrugated box as an alternative packaging material.

Transparent Superhydrophobic and Self-Cleaning Coating.

Surface roughness and low surface energy are key elements for the artificial preparation of biomimetic superhydrophobic materials. However, the presence of micro-/nanostructures and the corresponding increase in roughness can increase light scattering, thereby reducing the surface transparency. Therefore, designing and constructing superhydrophobic surfaces that combine superhydrophobicity with high transparency has been a continuous research focus for researchers and engineers. In this study, a transparent superhydrophobic coating was constructed on glass substrates using hydrophobic fumed silica (HF-SiO2) and waterborne polyurethane (WPU) as raw materials, combined with a simple spray-coating technique, resulting in a water contact angle (WCA) of 158.7 ± 1.5° and a sliding angle (SA) of 6.2 ± 1.8°. Characterization tests including SEM, EDS, LSCM, FTIR, and XPS revealed the presence of micron-scale protrusions and a nano-scale porous network composite structure on the surface. The presence of HF-SiO2 not only provided a certain roughness but also effectively reduced surface energy. More importantly, the coating exhibited excellent water-repellent properties, extremely low interfacial adhesion, self-cleaning ability, and high transparency, with the light transmittance of the coated glass substrate reaching 96.1% of that of the bare glass substrate. The series of functional characteristics demonstrated by the transparent superhydrophobic HF-SiO2@WPU coating designed and constructed in this study will play an important role in various applications such as underwater observation windows, building glass facades, automotive glass, and goggles.

X-ray crystallography derived diffraction properties of cuprite crystal as revealed by transmission electron microscopy

To produce high crystalline and unified cuprite nano single crystals from copper sulfate pentahydrate a unique bi-polarized methanol-water mixture reduces surface energy and enhances capping efficiency. Exhaustive significance lattice parameters, crystal volume, peak profiling, lattice constant, percent of crystallinity and crystal strain were analyzed by the whole powder pattern fitting (WFPP) Rietveld refinement method. A red shift at 636.0 nm in UV spectrophotometry is associated with a high surface plasmon effect and the zeta potential of 89.0 mV confirms the excellent stability of the cuprite crystal. Crystallographic data, d-spacing 0.25188 nm, lattice parameters a = b = c = 3.78 Å, α = β = γ = 90° of cuprite single crystal was further established by the selected area electron diffraction (SAED) in TEM. Energy dispersive spectroscopy (EDS) reveals the formation of the 100.0 % unified cuprite single crystal.

A rationally designed polymer brush/lubricant coating system for effective static and dynamic marine antifouling

Bioinspired slippery surfaces have garnered significant attention as promising solutions to mitigate biofouling. Unlike traditional lubricant-infused porous surfaces, recent research has focused on the integration of lubricants within polymer brush-grafted surfaces. The combination of polydimethylsiloxane (PDMS) polymer brush and silicone oil has gradually become the most prevalent choice due to their outstanding chemical affinity. However, this conventional coating system also has the potential for improvement to meet the needs of long-lasting and efficient marine antifouling, including i) precisely designing the polymer brush’s chemical structure to match the polarity of a specific lubricant enhances their chemical affinity, and ii) appropriately reduce the coating system’s surface energy to improve the fouling desorption performance. Here, we introduce a systematically engineered polymer brush/lubricant coating system that incorporates fluorinated polysiloxane and perfluoropolyether fluid. This novel coating system exhibits enhanced adhesion strength coupled with reduced surface energy, resulting in superior stability and omniphobic properties. Additionally, it showcases excellent corrosion resistance and significantly deters marine microorganism adhesion, achieving reductions of 98.8 % for P. tricornutum and 99.8 % for Bacillus sp.. Marine field trials, conducted over a 90-day static immersion period, confirm the remarkable antifouling performance, which surpasses most existing slippery coatings. Moreover, under dynamic conditions, organisms adhering for 150 days are readily dislodged by shear force. These findings underscore the pivotal role of systematic design in polymer brush/lubricant coating systems for the advancement of high-performance slippery surfaces tailored for marine antifouling applications.

Preferred Crystallographic Orientation via Solution Bathing for High‐Performance Inverted Perovskite Photovoltaics

AbstractThe meticulous control of crystal facets in polycrystalline perovskite films offers valuable insights into the photoelectric properties, varying significantly with different orientations. Exploring effective means to regulate these facets is crucial, and further revealing the underlying mechanisms is needed. Here, the research employed green solution bathing to obtain high‐quality perovskite films with preferred crystallographic orientation. In brief, eco‐friendly 2‐pentanol is used as the solvent, and functional molecules 2‐(dimethylaminomethyl)‐4‐(2‐aminoethylthiomethyl)thiazole (DAT) are introduced into the solution bathing as the solute. By introducing DAT molecules, precise control over perovskite crystal nucleation kinetics is achieved, resulting in films with a preferential (100) facet orientation. Conversely, films without DAT exhibited distinct (111) facet orientation. The regulation of DAT on perovskite film crystal facet is verified through theoretical and crystallographic analyses. Theoretical calculations show that S atom of DAT binds most strongly to the (100) facet of FAPbI3, promoting surface energy reduction and thermodynamic enhancement, favoring (100) crystal orientation. Crystallographic characterization further proved the regulation effect. In addition, PL/TRPL tests confirm the regulation of DAT on superior photoelectric properties of (100)‐oriented perovskite films. The work introduces a novel approach and preparation process for regulating the crystal facets orientation of polycrystalline perovskite films.

Effect of pore-bearing fluids on the mechanical behavior of siliceous cemented sandstones containing different clay contents and types

The clay minerals contained in the reservoir rock of CO2 geological storage formations can adsorb fluids and swell, which weakens the rock and promotes deformation. This phenomenon has not been widely investigated due to the complexity of the mineral components of the rock. To study the relationship between fluids in rock pores and the mechanical behavior of clay-bearing reservoir rocks, three types of siliceous cemented sandstones mainly composed of clay minerals and quartz, both dry and saturated with various fluids (i.e. N2, scCO2, H2O), were subjected to conventional triaxial compression tests. The results show that the fluids weakened the mechanical strength of the sandstones, and the degree of weakening depended on the clay composition and the type of fluid, with no significant relationship to the clay content. For the sandstone containing montmorillonite, compared to the dry condition, scCO2 and H2O reduced the peak strength by up to 7.16% and 15.33%, respectively, while for the sandstone containing only kaolinite as clay component, scCO2 and H2O reduced the peak strength by 3.34% and 3.18%, respectively. As a control, N2 weakened the strength of the three types of sandstones between 1.46% and 4.04%. By considering the failure characteristics of sandstone at the macro- and microscales, the failure mechanism of the sandstones was explained from two perspectives: the intercrack surface energy reduction and the swelling of clay. This study offers new perspectives for assessing the mechanical stability of fluid-bearing reservoirs and clarifies the role of clay in the connection between fluids in rock pores and the mechanical behavior of rocks.

INVESTIGATION OF SURFACE PROPERTIES OF MODIFIED BITUMEN COMPOSITIONS

One of the main reasons for premature destruction of road surfaces is the poor quality of road bitumen. An effective way to improve the quality of a bitumen binder is to modify it with polymer or surface-active additives. The goal is to determine the effect of the concentration of modifiers on surface tension in binary "bitumen-surfactant", "bitumen-polymer" and triple "bitumen-surfactant-polymer" systems. The methodology of the work included measuring the surface tension of modified bitumen systems depending on the quantitative content of additives in bitumen. Results and discussion: As follows from the analysis of the data obtained, in bitumen systems with a limited concentration of polymer AG-4I (C≤1 g/dm3), the effect of reducing surface energy at the interface with air is achieved by concentrating surfactants in the surface layer, which are part of the structure of the bitumen itself. The extreme nature of the change in surface tension was also recorded in AC-2 bitumen compositions. Conclusion: In the "bitumen-AG-4I-AS-2" triple systems, the change in the specific surface energy at the "liquid-gas" interface is not an additive value, taking into account the separate contribution of AG-4I and AS-2. The concentration threshold of additives to achieve a minimum surface tension varies in comparison with binary compositions. With the combined administration of AG-4I (C=1g/dm3) and AC-2 (C=1g/dm3), the surface tension decreased by 9.30 mN/m compared with unmodified bitumen.

Influence of Mechanical Loading on the Process of Tribochemical Action on Physicochemical and Biopharmaceutical Properties of Substances, Using Lacosamide as an Example: From Micronisation to Mechanical Activation.

Many physical and chemical properties of solids, such as strength, plasticity, dispersibility, solubility and dissolution are determined by defects in the crystal structure. The aim of this work is to study in situ dynamic, dispersion, chemical, biological and surface properties of lacosamide powder after a complete cycle of mechanical loading by laser scattering, electron microscopy, FR-IR and biopharmaceutical approaches. The SLS method demonstrated the spontaneous tendency toward surface-energy reduction due to aggregation during micronisation. DLS analysis showed conformational changes of colloidal particles as supramolecular complexes depending on the loading time on the solid. SEM analysis demonstrated the conglomeration of needle-like lacosamide particles after 60 min of milling time and the transition to a glassy state with isotropy of properties by the end of the tribochemistry cycle. The following dynamic properties of lacosamide were established: elastic and plastic deformation boundaries, region of inhomogeneous deformation and fracture point. The ratio of dissolution-rate constants in water of samples before and after a full cycle of loading was 2.4. The lacosamide sample, which underwent a full cycle of mechanical loading, showed improved kinetics of API release via analysis of dissolution profiles in 0.1 M HCl medium. The observed activation-energy values of the cell-death biosensor process in aqueous solutions of the lacosamide samples before and after the complete tribochemical cycle were 207 kJmol-1 and 145 kJmol-1, respectively. The equilibrium time of dissolution and activation of cell-biosensor death corresponding to 20 min of mechanical loading on a solid was determined. The current study may have important practical significance for the transformation and management of the properties of drug substances in solid form and in solutions and for increasing the strength of drug matrices by pre-strain hardening via structural rearrangements during mechanical loading.

Effect of CO2-H2O Interaction with High-Rank Coal on Mechanical Properties and Acoustic Emission Characteristics under Confining Pressure.

The adsorption of CO2 by coal leads to changes in its mechanical properties, particularly when considering supercritical CO2 and water with supercritical CO2 adsorption. This is strongly linked to the efficiency of CO2-enhanced coalbed methane (CO2-ECBM) extraction and the safety of CO2 geological storage. This study focuses on 3# coal from the Datong Mine in Gaoping City, Shanxi Province. The high-rank coal's mechanical properties, including the triaxial compressive strength and elastic modulus, were examined under the combined effects of CO2 injection pressure, CO2 injection time, and moisture content. The triaxial compressive strength and elastic modulus of the coal showed a decrease following CO2 injection. Increasing the CO2 injection pressure, prolonging the CO2 injection time, and increasing the moisture content were favorable for coal softening. In particular, the triaxial compressive strength and elastic modulus of the coal sample after 144 h of water and supercritical CO2 softening decreased by 67.67 and 64.15%, respectively. Injecting CO2 into coal changed its failure mode. The dry raw coal sample exhibited a brittle shear failure mode, while the coal samples showed transitional shear failure after injecting 6 MPa CO2 and 8 MPa CO2 and ductile nondilatant barreling failure after injecting water and 8 MPa CO2 (with a moisture content of 3.02%). Moreover, the cumulative acoustic emission energy of the coal samples followed a similar trend to the decrease in mechanical properties under different conditions. The physical and chemical interactions among coal, CO2, and water caused the softening of coal; these included the generation of the swelling stress, the dissolution of minerals by carbonate solutions, the reduction in surface energy of coal owing to CO2 adsorption, and the extraction and plasticization reactions of organic matter in coal. The research results are of great significance for further understanding CO2-ECBM and CO2 geological sequestration.