Contact Angle Test Research Articles

Optimizing biomimetic hydroxyapatite coating on Ti-6Al-6Mo alloy: influence of immersion time

This study investigates the formation and characteristics of hydroxyapatite (HAp) coating on Ti-6Al-6Mo alloy through immersion in a supersaturated calcification solution (SCS) for 3, 7, and 14 days. X-ray diffraction (XRD) and secondary electron microscopy (SEM) with electron dispersive spectroscopy (EDS) were used to identify the phases and characterize the morphology and composition of the HAp layer. Atomic force microscopy (AFM) and contact angle tests were used to evaluate the surface properties, while potentiodynamic corrosion testing in Hanks’ solution was used to assess corrosion behavior. It is confirmed that the sample immersed for 14 days formed an HAp layer on the Ti-6Al-6Mo substrate with a Ca/P ratio of 2.5, approaching the ideal value of 1.67. This HAp film exhibits a smooth and homogeneous crystal structure, with a surface roughness of 31.47 nm and an appreciable corrosion rate of 0.0005 mm y−1. This study signifies the impact of immersion time on the microstructural properties and biocompatibility of biomimetic HAp coatings applied to Ti-6Al-6Mo alloy, contributing to the progress of HAp coatings in biomedical engineering.

Exploration on performance of the oxidized collector in the low-rank coal flotation

ABSTRACT Low-rank coal can be concentrated by flotation process using oxidized kerosene, which can improve flotation performance. However, the difference between oxidized kerosene and conventional collector with the same dosage on flotation performance is little known. In this study, the FTIR spectrum, GC-MS analysis and surfaces tension of collectors were analyzed for comparison the physical and chemical properties. The results showed the kerosene appearance of the short hydrocarbon chains with oxygen groups. The surface tension of kerosene is reduced by 21.99 mm/m after oxidation process. The contact angle and flotation tests were used for the kerosene, mixture including oxidized kerosene and kerosene with a mass ratio of 1:1, as well as oxidized kerosene for evaluating the performance. The results showed that the order of coal surface contact angle is that kerosene > mixture > oxidized kerosene. In addition, flotation tests revealed that mixture had superior flotation performance compared with kerosene and oxidized kerosene. The oxidized kerosene could significantly diminish the ash content of flotation concentrates, and the combustible matter recovery of clean coal with mixture is nearly 16.50% higher than that with kerosene. These results constitute a substantial step forward in technical development for resource recycling of low-rank coal.

Synthesis of Amphiphilic Polyacrylates as Peelable Coatings for Optical Surface Cleaning

Optical instruments require extremely high precision, and even minor surface contamination can severely impact their performance. Peelable coatings offer an effective and non-damaging method for removing contaminants from optical surfaces. In this study, an amphiphilic polyacrylate copolymer (PMLEA) was synthesized via solution radical copolymerization using the lipophilic monomer lauryl acrylate (LA) and hydrophilic monomers ER-10, methyl methacrylate (MMA), and butyl acrylate (BA). The structure and molecular weight of the copolymer were characterized using Fourier transform infrared spectroscopy (FTIR), nuclear magnetic resonance (NMR), and gel permeation chromatography (GPC). The hydrophilic–lipophilic balance, surface tension, and wettability of the copolymer were analyzed through water titration, the platinum plate method, and liquid contact angle tests. The cleaning performance of the copolymer coating on quartz glass surface contaminants was evaluated using optical microscopy and Ultraviolet-Visible Near-Infrared (UV-Vis-NIR) spectroscopy. The study examined the effect of varying the ratio of LA to ER-10 on the hydrophilicity, lipophilicity, cleaning efficiency, and mechanical properties of the copolymer coating. The results showed that when the mass ratio of LA to ER-10 was 1:2, the synthesized copolymer exhibited optimal performance in removing dust, grease, and fingerprints from quartz glass surfaces. The coating had a tensile strength of 2.57 MPa, an elongation at break of 183%, and a peeling force of 2.07 N m−1.

Polyglycerol Sebacate/polycaprolactone/reduced graphene oxide composite scaffold for myocardial tissue engineering

The aim of this research was to fabricate and evaluate polyglycerol sebacate/polycaprolactone/reduced graphene oxide (PGS-PCL-RGO) composite scaffolds for myocardial tissue engineering. Polyglycerol sebacate polymer was synthesized using glycerol and sebacic acid prepolymers, confirmed by Fourier-transform infrared spectroscopy (FTIR) and X-ray diffraction (XRD). Six PGS-PCL-RGO composite scaffolds (S1-S6) with various weight ratios were prepared in chloroform (CF) and acetone (Ace) solvents at 8 CF:2Ace and 9 CF:1Ace volume ratios, using the electrospinning method at a rate of 1 ml/h and a voltage of 18 kV. The scaffolds' chemical composition and microstructure were characterized by FTIR, XRD, and scanning electron microscopy (SEM). Further investigations included tensile testing, contact angle testing, four-point probe testing for electrical conductivity, degradation testing, and cytotoxicity testing (MTT). The results showed that adding 2%wt RGO to the composite scaffold decreased fiber diameter and degradation rate, while increasing electrical conductivity and ductility. The 33%PGS-65%PCL-2%RGO (S3) composite scaffold exhibited the lowest degradation rate (23.87 % over 60 days) and the highest electrical conductivity (51E-3 S/m). Mechanical evaluations revealed an elastic modulus of 2.46 MPa and elongation of 62.43 %, aligning closely with the heart muscle's elastomeric properties. The contact angle test indicated that the scaffold was hydrophilic, with a water contact angle of 61 ± 2°. Additionally, the cell toxicity test confirmed that scaffolds containing RGO were non-toxic and supported good cell viability. In conclusion, the 33%PGS-65%PCL-2%RGO composite scaffold exhibits mechanical and structural properties similar to heart tissue, making it an ideal candidate for myocardial tissue engineering.

Preparation of Antistatic Polyester Fiber via Layer-by-Layer Self-Assembly

Polyester fibers tend to generate static electricity during the weaving and application processes, posing a threat to their production. Enhancing the water absorbency and electrical conductivity of polyester fibers themselves is an effective approach to improving their antistatic properties. In this study, multifunctional chitosan (CS), sodium phytate (SP), and Cu2+ were loaded on polyester fibers through layer-by-layer (LBL) self-assembly. The antistatic and water absorption capability of the modified polyester fibers was investigated by designing different process parameters combined with a surface resistance test and water contact angle tests. The antistatic property test results confirmed the positive effect of CS and Cu2+ on discharging electrostatic charge. Within a definite scope, with the increase in the number of assembly layers, assembly duration, and the concentration of the assembly substances, the wettability of the modified polyester fibers became more favorable and the antistatic effect became more remarkable.

Preparation, Mechanical and Thermal Insulation Properties of Graphene Oxide/Polydopamine/Polyurethane Foam‐Based Tunnel Insulation Liner Material

This article designs a novel tunnel insulation liner material based on polyurethane foam (PUF), aiming to improve the liner material's mechanical properties, hydrophobicity, thermal insulation properties and to reduce the self‐weight of the material. Firstly, PUF is self‐made using a one‐step method, and the optimal parameter combination is optimized through the single‐parameter (SP) method. Secondly, based on the optimal parameter combination of PUF, a new process is employed to prepare polydopamine (PDA)/graphene oxide (GO)/PUF. Compression experiments and contact angle tests are conducted to assess the physical mechanical properties of PDA/GO/PUF. Infrared thermography and combustion experiments are employed to characterize the thermal insulation performance of PDA/GO/PUF. Microscopic mechanisms are explained through thermogravimetric analysis (TG), scanning electron microscopy (SEM), and Fourier‐transform infrared spectroscopy (FTIR). The results show that: the optimal parameter combination of tin(II) bis(2‐ethylhexanoate) (TEH), water (H2O), and toluene‐2,4‐diisocyanate (TDI) content optimized by the SP method is 4 parts, 2.8 parts, and 19 parts. PUF prepared based on the optimal parameter combination exhibits a dense and uniform cell structure with low density. Under cyclic loading, PDA/GO/PUF composite material exhibits excellent mechanical stability and fatigue resistance; the hydrophobicity, thermal insulation, and thermal stability of PDA/GO/PUF are significantly improved compared to PUF.

Surface amphiphilic hybrid porous polymers based on cage-like organosiloxanes for pipette tip solid-phase extraction of microcystins in water

The occurrence of microcystins (MCs) during harmful algal blooms (HABs) represents a major threat to freshwater environments. In this work, a novel surface amphiphilic hybrid porous polymers based on cage-like organosiloxanes (PCSs) was prepared for the enrichment of MCs. The copolymerization of bifunctional amphiphilic monomers, 2-methacryloyloxyethyl phosphorylcholine (MPC) and N-benzylquininium chloride (BQN), with the cross-linker methacryl substituted polyhedral oligomeric silsesquioxane (POSS) was achieved in an ionic liquid-based porogenic medium. The hierarchical porous structure, a variety of surface functional groups and weak hydrophilicity were well characterized on the prepared materials using scanning electron microscopy, nitrogen adsorption/desorption analysis, Fourier transform infrared spectroscopy, X-ray photoelectron spectroscopy, zeta potential analysis and water contact angle testing, respectively. The as-prepared surface amphiphilic PCSs was used as an adsorbent for pipette tip solid-phase extraction (PT-SPE) to enrich microcystins (MCs) from surface waters before their analysis by capillary electrochromatography (CEC) and liquid chromatography-mass spectrometry (LC-MS). Under the optimal conditions, the established PT-SPE-LC-MS method exhibited a wide linear range (10–10,000 ng L−1), low limits of detection (4.0–8.0 ng L−1) and satisfactory recoveries (89.5–102.8 %) for MCs. An adsorption mechanism involving electrostatic interactions, hydrogen bonding, hydrophilic interactions, and π-π stacking has been proposed. The findings suggest that the use of surface amphiphilic PCSs materials as adsorbents in the PT-SPE platform facilitates efficient enrichment of MCs for subsequent chromatographic analysis. These investigations offer a new perspective on the simple and uncomplicated pretreatment of complex environmental samples.

Fabrication and Self-Assembly Behavior of BPEF and BBPEF Composite Langmuir-Blodgett Films with Photovoltaic Conversion Properties.

The LB films prepared through the Langmuir-Blodgett (LB) technique are of significant importance for the fabrication of functional films such as optoelectronic materials and sensors. In this study, 9,9-bis (4-(2-hydroxy-ethoxy) phenyl) fluorene (BPEF) and 9,9-bis [3-phenyl-4-(β-hydroxy-ethoxy) phenyl] fluorene (BBPEF) were combined with saffron T (ST), methylene blue (MB) and Rhodamine B (RhB) dyes by LB technique to prepare ordered composite films. The nanostructures and morphologies of the composite films were analyzed by transmission electron microscopy (TEM) and atomic force microscopy (AFM). It was found that the films exhibited distinct aggregation morphologies. The UV-VIS absorption spectra showed that the concentration of dye molecules had a significant effect on the spectral characteristics. The contact Angle test shows that the prepared composite films are hydrophobic. The photovoltaic conversion performance of LB composite films was studied by transient photocurrent response experiments. It was found that BPEF/dye and BBPEF/dye composite films exhibited significant responses in photocurrent. In particular, BPEF/RhB and BBPEF/RhB composite films demonstrated excellent photoresponsive performance. This study used LB technology in combination with BPEF and BBPEF to demonstrate enhanced photocurrent and stable performance of LB film, which provided ideas for expanding the application range of materials.

Optimizing activated carbon electrodes and improving their electrochemical performance through nitrogen doping and HNO3 modification

In order to optimize the process conditions, electrodes were prepared by mixing coal-based activated carbon (AC), polyvinylidene fluoride (PVDF), and conductive carbon black on a graphite plate. To enhance the adsorption capacity of the electrode, nitrogen-doped modification and nitric acid modification were sequentially performed on AC. Characterization methods included scanning electron microscopy (SEM), specific surface area (BET), x-ray photoelectron spectroscopy (XPS), and other analytical techniques. Contact angle and cyclic voltammetry tests were also conducted on the electrode. The experimental results showed that the modified material's specific surface area increased from 482.843 m2/g to 856.073 m2/g, the electrode's specific capacitance reached 404.56 F/g. For better utilization of AC for electrosorption, new nitrogen- and oxygen-containing functional groups were introduced to provide additional electrons, reduces the internal resistance of the material improves the electron mobility, and improves AC electrochemical performance. The removal of Cu2+ by modified AC reached 76.25 % at a Cu2+ concentration of 80 mg/L with an applied voltage of 1.5 V.

Physical, chemical, and biological property of silk reinforced polycaprolactone composites for bone tissue engineering

To develop a biodegradable implantable bone material with compatible mechanics with the bone tissue, providing a new biomaterial for clinical bone repair and regeneration. Silk reinforced polycaprolactone composites (SPC) containing 20%, 40%, and 60% silk were prepared by layer-by-layer assembly and hot-pressing technology. Macroscopic morphology was observed and microstructure were observed by scanning electron microscopy, compressive mechanical properties were detected by compression test, surface wettability was detected by surface contact angle test, degradation of materials was observed after soaking in PBS for 180 days, and proliferation of MC3T3-E1 cells was detected by cell counting kit 8 assay. Six Sprague Dawley rats were subcutaneously implanted with polycaprolactone (PCL) and 20%-SPC, respectively. Masson staining was used to analyze the in vivo degradation behavior and vascularization effect within 180 days. The pore defects of the three SPC sections were relatively few. In the range of 20% to 60%, as the silk content increased and the PCL content decreased, the interlayer spacing of silk fabric decreased, and the fibers almost covered the entire cross-section. The compressive modulus and compressive strength of SPC showed an increasing trend, and the compressive modulus of 60%-SPC was slightly lower than that of 40%-SPC. There were significant differences in compressive modulus and compressive strength between the materials ( P<0.05). In vitro simulated fluid degradation experiments showed that the mass loss of the three types of SPC after 180 days of degradation was within 5%, with the highest mass loss observed in 60%-SPC. The differences in mass loss between the materials were significant ( P<0.05). As the silk content increased, the static water contact angle of each material gradually decreased, and all could promote the proliferation of MC3T3-E1 cells. The subcutaneous degradation experiment in rats showed that 20%-SPC began to degrade at 30 days after implantation, and material degradation and vascularization were significant at 180 days, which was in sharp contrast to PCL. SPC has the mechanical and hydrophilic properties that are compatible with bone tissue. It maintains its mechanical strength for a long time in a simulated body fluid environment in vitro, and achieves dynamic synchronization of material degradation, tissue regeneration, and vascularization through the body's immune regulation mechanism in vivo. It is expected to provide a new type of implant material for clinical bone repair.

Investigation of immobilized RAP binder on asphalt-asphalt/aggregate interaction under multiple temperatures

The traditional blending process includes blending recycled asphalt pavement (RAP) aggregates and virgin aggregates first and then adding the virgin binder. In the first blending process, the mobilized RAP binder coated virgin aggregates, and the immobilized RAP binder remained RAP aggregates. The objective of this study was to investigate the role of the immobilized RAP binder in the mixing process. The contact angle test and binder bond strength (BBS) test were utilized under multiple temperature conditions to discuss the interaction behavior between immobilized RAP binder and virgin binder/aggregate. Results showed that at 90–170 °C, the spreading degree and rate of contact angle between virgin binder and immobilized RAP binder was bigger and higher than that between virgin binder and virgin aggregate, which indicated that the contact behavior between virgin binder and RAP aggregate was stronger than that between virgin binder and virgin aggregate. But at 50–90 °C, the changes in contact behaviors were unstable and irregular. In BBS test, at 20–60 °C, the bonding strength between virgin binder and slate coated by immobilized RAP binder was higher than that between virgin binder and clean slate. At 0–20 °C, the BBS of former was slightly smaller than that of latter. It was believed that the immobilized RAP binder on the surface of RAP aggregate could promote more effective wetting effect between RAP aggregates and virgin binder during mixing, which was better than that between virgin binder and virgin aggregate.

Effect of silica‐loaded polydopamine‐modified graphene oxide nanocomposites on the corrosion resistance of polyester coatings

AbstractOn the basis of the complex environment of port terminals, the corrosion resistance of coatings for accompanying metal facilities is a primary factor that needs to be considered. This study prepared polydopamine‐modified graphene oxide loaded with silicon dioxide (PGO@SiO2) functional filler, which was incorporated into polyester resin (PR) by extrusion mixing. The PGO@SiO2/PR composite coating was obtained by electrostatic spraying and high‐temperature curing. Fourier transform infrared spectroscopy, x‐ray diffraction, and other results confirmed the successful preparation of the PGO@SiO2 functional filler. In addition, contact angle, adhesion, and corrosion resistance tests were performed on the composite coating. Compared with pure PR coating, the surface hydrophobicity and adhesion of the composite coating were significantly improved compared with the pure PR coating. Furthermore, the electrochemical impedance spectroscopy of the carbon steel substrate composite coating confirmed that after immersion in salt solution, the low‐frequency impedance modulus of the composite coating could be maintained at 8.63 × 108 Ω·cm2, which was more than two orders of magnitude higher than that of the pure PR coating. Thus, PGO@SiO2 could significantly enhance the corrosion resistance of the PR coating and hinder the infiltration of corrosive media. It has broad prospects for engineering applications because of its excellent anticorrosive performance.

Evaluating diffusivity for efficient electrocatalytic conversion of carbon dioxide into multicarbon products using dealloyed hierarchically nanoporous copper

Hierarchical nanoporous copper (Hi-NPC) is a promising catalyst for carbon dioxide reduction reaction (CO2RR) due to its high surface area and excellent mass transport properties. To evaluate the effect of its architecture, eutectic-phased Cu18Al82 and single-phased Cu33Al67 were potentiostatically dealloyed to produce Hi-NPC and homogeneous nanoporous copper (Ho-NPC), respectively. At a comparable overpotential, the Hi-NPC electrocatalyst exhibited a significantly higher C2+ partial current density (jC2+) in CO2RR, reaching 510 mA/cm2, compared to both Ho-NPC (72 mA/cm2) and Cu electrodes (23 mA/cm2). When the current density was normalized by the electrochemically active surface area, the CO production among three electrodes demonstrated similar electrochemical behavior. However, notable differences were observed in the formation of C2H4 and C2H5OH, which can be attributed to the hierarchical structure of Hi-NPC facilitating C–C coupling to form C2 products. Although the Tafel plot indicated the CO2RR kinetics were identical for all three electrodes, linear sweep voltammetry experiments revealed that Hi-NPC exhibited the steepest current variation slope. Furthermore, the improved diffusivity was further confirmed by conducting oxygen reduction reactions with varying partial O2/N2 flow rates and electrochemical impedance spectroscopies. The hydrophobic properties of the electrode under various CO2RR current densities were also evaluated by water contact angle test.

Characterization and comparability study of a series of novel fluorinated polyacrylates with a rigid cyclohexane mesogenic core

Surface reconstruction has always been a pain point in the study of short-chain perfluoroalkyl acrylate polymers, and how to maintain the balance between environmental protection and good performance is the key issue. We exploited the high efficiency and selectivity of the reaction between the isophorone di-isocyanate group and the hydroxyl group, and the rigid cyclohexane structure contained in their molecule to efficiently prepare a series of novel fluoro acrylate monomers (IFAM) containing rigid cyclohexane as mesogenic core and their homopolymers (PIFAM) with different lengths of short-chain perfluoroalkyl side chains. Their structures, liquid crystal behavior, thermal properties, surface chemical compositions, surface morphologies, and hydrophobicity were characterized and comparatively studied by FTIR, NMR, XRD, POM, DSC, TGA, XPS, AFM, and static/dynamic contact angle tester and dodecafluoroheptyl methacrylate (DFMA) and its homopolymer as a contrast. The results demonstrated that both the synthesized monomers and homopolymers possessed the expected chemical structures with thermotropic liquid crystalline behavior. Furthermore, the thermal stability and hydrophobicity of the polymers increased with the extension of the fluorocarbon chain length. The incorporation of the mesocrystalline motif and appropriate length of fluoroalkyl tails in the PIFAM polymers would enhance hydrophobic stability, as it promoted the crystallinity of the side chains and limited the structural rearrangement of the fluorocarbon chains. This study offers a straightforward method for synthesizing fluoro acrylate polymers with stable surface properties, highlighting their potential application in hydrophobic coatings.

Bioinspired surface silicification of cellulose-mediated PVDF membranes for significantly enhancing superhydrophilicity and anti-oil adhesion toward ultrafast oil/water emulsion separation

Cellulose is a widely used hydrophilic material due to its rich hydrophilic hydroxyl groups. However, the presence of its lipophilic segment will affect the antifouling performance. Finding strategies to improve this problem has attracted considerable attention. In this work, a layer of silica was applied to a cellulose-deposited polyvinylidene fluoride membrane through a straightforward in-situ bionic silicification process of tetraethyl orthosilicate. The contact angle and oil droplet contact test proved that the high-hydrophilicity and underwater superoleophobicity of the silicified membranes were significantly enhanced. The surface structure and composition were analyzed by scanning electron microscopy, Fourier transform infrared spectroscopy and X-ray photoelectron spectroscopy. The results of show that this improvement was mainly attributed to the presence of silicon hydroxyl groups, buried cellulose chains, and micro-nanostructures composed of cellulose and silica. The stable silica coating also provided protection for the polymeric membrane against degradation after water washing for 24 h, ultrasonic treatment (40 KHZ) for 10 min or exposure to different pH levels (pH=1, 4, 9 and 12) and saturated sodium chloride solution for 24 h. Furthermore, the silicified membrane showed outstanding oil adhesion resistance and permeation flux, enabling effective purification of different oil-in-water emulsions that were stabilized by emulsifiers. Notably, the membrane achieved a high oil removal rate (> 99.4 %) of various emulsions (toluene-in-water, cyclohexane-in-water, tetrachloroethane-in-water, soybean oil-in-water, toluene-in-salt solution, toluene-in-acid solution and toluene-in-alkaline solution emulsions). In particular, for toluene-in-water emulsions (oil droplets in the emulsion ranged from 58.77 nm to 615.1 nm), a significantly enhanced permeation flux (4777 L·m−2·h−1·bar−1) was obtained at 0.8 bar pressure. Even after multiple cycles of separation, the flux was higher than that of the unsilicified membrane. Overall, this approach is mild, simple, efficient, and easily scalable, making it an ideal method for producing superhydrophilic coatings with substantial application potential.

Application and mechanistic insights of a washing/microwave/ultrasonic ternary pretreatment for enhancing barite flotation in waste drilling fluids

A quantity of recoverable barite exists in high-density waste drilling fluid. Based on the inefficiencies and complexities of existing recycling methods, a novel pre-treatment approach which includes clean-breaking, high-speed washing, ultrasonic dispersion, and microwave heating and a new depressant (Gellan Gum) was proposed. The floatability, separation efficiency and mechanism were discussed by SEM, adsorption capacity, zeta potential measurements and contact angle tests. The results of reverse flotation experiments results indicated that secondary water washing proves highly effective in enriching a significant quantity of barite solid phase. Subsequent microwave-ultrasonic and flotation can obtain barite of high quality with recovery and density reaching 81.5% and 4.238 g/cm3, respectively. It can be utilized directly in the preparation of drilling fluid. Mechanism studies shown that the per-treatments substantially enhances the barite grade while effectively eliminating low-density solid phases adhering to the barite surface, thus exposing additional contact points between the constituents so as to improve flotation separation. This new recovery scheme has environmental advantages and great reference value for the separation of barite within high-density waste drilling fluids.

Development of a Superhydrophobic Protection Mechanism and Coating Materials for Cement Concrete Surfaces.

In order to further enhance the erosion resistance of cement concrete pavement materials, this study constructed an apparent rough hydrophobic structure layer by spraying a micro-nano substrate coating on the surface layer of the cement concrete pavement. This was followed by a secondary spray of a hydroxy-silicone oil-modified epoxy resin and a low surface energy-modified substance paste, which combine to form a superhydrophobic coating. The hydrophobic mechanism of the coating was then analysed. Firstly, the effects of different types and ratios of micro-nano substrates on the apparent morphology and hydrophobic performance of the rough structure layer were explored through contact angle testing and scanning electron microscopy (SEM). Subsequently, Fourier transform infrared spectroscopy and permeation gel chromatography were employed to ascertain the optimal modification ratio, temperature, and reaction mechanism of hydroxy-silicone oil with E51 type epoxy resin. Additionally, the mechanical properties of the modified epoxy resin-low surface energy-modified substance paste were evaluated through tensile tests. Finally, the erosion resistance of the superhydrophobic coating was tested under a range of conditions, including acidic, alkaline, de-icer, UV ageing, freeze-thaw cycles and wet wheel wear. The results demonstrate that relying solely on the rough structure of the concrete surface makes it challenging to achieve superhydrophobic performance. A rough structure layer constructed with diamond micropowder and hydrophobic nano-silica is less prone to cracking and can form more "air chamber" structures on the surface, with better wear resistance and hydrophobic performance. The ring-opening reaction products that occur during the preparation of modified epoxy resin will severely affect its mechanical strength after curing. Controlling the reaction temperature and reactant ratio can effectively push the modification reaction of epoxy resin through dehydration condensation, which produces more grafted polymer. It is noteworthy that the grafted polymer content is positively correlated with the hydrophobicity of the modified epoxy resin. The superhydrophobic coating exhibited enhanced erosion resistance (based on hydrochloric acid), UV ageing resistance, abrasion resistance, and freeze-thaw damage resistance to de-icers by 19.41%, 18.36%, 43.17% and 87.47%, respectively, in comparison to the conventional silane-based surface treatment.

Disintegration behaviors of red clay under wet-dry cycles

Cyclic wetting-drying alternation has a significant influence on the strength and structure of soils. It is prone to causing soil softening and disintegration, highlighting the importance to improve the soil's resistance to disintegration. This paper utilizes a self-developed disintegration test apparatus to analyze the disintegration characteristics of improved red soil under wet-dry cycles, focusing on the disintegration amount and ratio. Furthermore, XRD (X-ray diffraction), SEM (scanning electron microscope), tensile test, and contact angle test are employed to investigate the anti-disintegration behaviors of the improved red soil. The results show that the disintegrating amount and ratio of undisturbed and improved red soil are distinctly different under wet-dry cycles. Linear, stepped, constant and concave but perfect "S" shapes of the disintegrating ratio are observed in the cyclic tests. Cement and lime strengthen the red soil primarily through hydration reaction. The drop experiment confirms that cement plays a crucial role in restraining the disintegration. When the ameliorant content is low, the correlation between pore parameters and disintegration duration of red soil follows the order: mean shape coefficient > fractal dimension > probability entropy > area probability distribution index. With a high ameliorant content, the correlation remains similar, with slightly higher correlation for probability entropy. Under wet-dry cycle conditions, sludge and kaolin can improve the soil through the bonding of clay particles. The improved water repellency greatly enhances the resistance to disintegration of the altered red soil. The research provides valuable insights for the practical application of soil.

Research on the process of preparing fiber filtration membrane by centrifugal blowing electrospinning technology

AbstractCurrently, the problem of air pollution is getting more and more serious, especially the pollution of tiny solid particles (PM, particulate matter) in the air, which poses a great challenge to the environment and human health. Therefore, it is particularly important to develop air filtration materials with high filtration efficiency and low resistance to meet this challenge. In this study, we propose to prepare air filtration membranes by centrifugal jet electrospinning technology, design multifactorial orthogonal coupling experiments, and investigate the effects of key process parameters of centrifugal jet electrostatic spinning, including solution concentration, airflow rate, rotational speed, and voltage, on the fiber diameter and uniformity by applying the polar analysis of variance and analysis of variance. PAN‐BaTiO3 electret nanofiber filtration membranes with high efficiency and low resistance were prepared by combining the optimized process of centrifugal blowing electrospinning. Various characterization methods (tensile test, water contact angle test, surface charge test, filtration test) were used to evaluate the effect of different BaTiO3 electret contents (0%, 0.1%, 0.5%, 1%) on the comprehensive performance of the filtration membranes, and the electret filtration efficiency of the electret filtration membranes prepared by the present process reached as high as 96.56% with a pressure drop of 29 Pa.

A simple method for preparing Sb2S3/short-cut carbon fiber foam for the electrocatalytic degradation of dyes

The unstarched short-cut carbon fiber (SCF) foam modified with Sb2S3 nanoparticles (Sb2S3/SCF foam) was synthesized by melamine foam as a template to apply in electro-degradation of methyl orange (MO) and a mixture of dyes. This process takes full advantage of the self-supported 3D SCF foam's mechanical stability and electrical conductivity while preventing the aggregation of unstarched SCF and Sb2S3 nanoparticles. The in-situ deposition and good dispersion of Sb2S3 nanoparticles expose catalytic active sites synergy with stable free-standing 3D SCF foam resulting in efficient degradation capability. The morphology, composition, structure, and hydrophilicity of Sb2S3/SCF foam were analyzed using SEM, EDS, XPS, XRD, Raman, PL, BET and contact angle tests. The Sb2S3/SCF foam is highly effective for degrading MO, with a degradation rate of 97.92 % achieved in just 4 hours at 2.4 V (vs. SCE). Additionally, it could simultaneously degrade mixed dyes including methyl orange (MO), crystal violet (CV), and methylene blue (MB) within 5 hours, achieving complete fade. Furthermore, the Sb2S3/SCF foam also possesses desirable features for large-scale practical applications and recycling in dye degradation.