Excellent Wettability Research Articles

The SCC behavior of MAO/EPD biocomposite coatings on Ti-6Al-4V alloy

Aseptic loosening and inadequate osseointegration are significant issues associated with titanium alloy implants in complex body fluid environments. Surface coatings techniques are often employed to enhance the bioactivity and osseointegration capabilities. In this research, biocomposite coatings were fabricated on Ti-6Al-4V alloy employing micro-arc oxidation (MAO) and the integration of micro-arc oxidation/electrophoretic deposition (MAO/EPD) technology. Microstructure, bioactivity, and corrosion resistance of the coatings were studied. To investigate the effect of the coatings on the stress corrosion cracking (SCC) behavior of Ti-6Al-4V alloy, slow strain rate tension (SSRT) tests were conducted in simulated body fluid (SBF). Results show that the adhesive strength of the MAO/EPD composite coatings is around 28.41N, with an average contact angle of 19.05 °, indicating excellent wettability and biocompatibility. The corrosion rate of biocomposite coatings is 3.43 μm·a−1 and the biocomposite coatings exhibit excellent SCC resistance, with a SCC sensitivity of 9.21%, which is significantly lower than the 18.39% of Ti-6Al-4V alloy. This can be attributed to the lower porosity of the coatings, which can provide excellent protection for the alloy.

Organic Salt Buffer Layer Enables High‐Performance NiOx‐Based Inverted Perovskite Solar Cells

The merits of a low‐cost fabrication process, suitable band structure, excellent wettability to perovskite precursor, and outstanding stability ensure NiOx as a hole transport material with beneficial characteristics to construct high‐performance perovskite solar cells (PSCs). However, direct contact between perovskite and NiOx causes delamination and chemical instability and thus results in poor carrier transport and short device lifespan. Here, we propose a solution for this issue by introducing an organic salt additive 4‐(trifluoromethyl) benzylammonium formate (TFMBAFa) in the perovskite precursor to passivate perovskite film and NiOx@(2‐(3,6‐dimethyl‐9H‐carbazol‐9‐yl) ethyl) phosphonic acid (Me‐2PACz) composited hole transport layer (HTL), and thus construct a buffer layer between perovskite‐HTL interface. The effective diminishing of NiOx/perovskite interfacial reactions and defects results in enhanced carrier transport. Consequently, the target device achieves simultaneous improvements in power conversion efficiency (24.2%), storage stability (T100 > 1400 h), thermal stability (T80 > 1000 h), and operational stability (T70 > 850 h), where T100, T80, and T70 refer to the retention of 100%, 80%, and 70% of initial PCE, respectively. This work provides an effective strategy to advance the performance of NiOx‐based inverted PSCs.

Turning Crisis into Opportunity: Intrinsically Polarised Low Concentration Eutectic Electrolytes Enable Highly Reversible Zinc Anodes

Low-concentration electrolytes (LCEs) hold great promise for sustainable energy storage due to their low viscosity, excellent wettability, and cost-effectiveness. However, their intrinsic polarization issues often lead to side reactions and dendrite growth, hindering their broader application. Herein, we present an approach to convert the negative effects of intrinsic polarization in LCEs into advantages, overcoming these challenges. The experimental and theoretical analyses demonstrate that acetate-adsorbed zinc anodes can harness the intrinsic polarization of LCEs to direct the electrocrystallization process on their surfaces. This promotes the preferential orientation of Zn(002) plane with high stability, resulting in symmetric batteries loaded with low-concentration eutectic electrolytes (LCEE) that maintain surprisingly low voltage polarization during the dendrite-free growth of up to 3150 h. In addition, by forming an organic-inorganic composite film enriched with N and Cl, LCEE achieves rapid migration of Zn2+. This allows Zn//PANI full batteries with LCEE to demonstrate superior capacity and cycling stability compared to other Zn-based batteries with LCEs. This study not only achieves a divergent design in LCEs but also provides clear guidance for future electrolyte development.

Surface treatment processed electron transport layers for efficient Sb2S3 solar cells

Solution-processed Sb2S3 thin films and solar cell devices have recently gained popularity due to their easy procedure and outstanding final device performance. Nevertheless, although the substrate has a significant influence on thefollowing functional films, the effect of the substrate in the Sb-based solar cells appears to have not been adequately examined. In this study, we performed an interesting thioacetamide (TA)-assisted surface treatment strategy on the electron transport layer (ETL) to achieve high-quality development of Sb2S3 thin films and based solar devices. The surface treatment of ETLs resulted in a uniform surface, Zn(OH)2 impurity reduction, and excellent wettability. The above enhanced the growth of Sb2S3 thin films with features like extremely large crystal sizes (∼8 um), more homogeneous and dense film morphology, preferred crystal orientation, reduced oxygen content, and fewer defects, which benefits carrier transport. Finally, a device structure constructed of FTO/TiO2/Zn(O,S)/Sb2S3/Spiro/Au was created, resulting in an almost 30 % increase in efficiency, from 4.05 % to 5.21 %. The proposed approach not only gives new insights into generating higher-quality Sb2S3 thin films and devices, but it also presents new concepts and methods for future high-quality sulfide thin film preparation.

Densification and properties of WC-CoCrFeNi/Co cemented carbide fabricated via spark plasma sintering

The spark plasma sintering (SPS) technique was used to employe WC-CoCrFeNi/Co cemented carbides, incorporating CoCrFeNi and Co as low-coercivity binder phases, resulting in the development of cemented carbides with exceptional mechanical properties. The densification mechanism varying with increasing sintering temperature and the effect of densification on the mechanical properties were investigated using the creep deformation model. In the temperature range of 1100 °C–1300 °C, the main factors contributing to densification behavior are particle rearrangement and grain boundary diffusion due to the viscous flow of the binder phase. The densification mechanism gradually transforms into dislocation climbing with increasing temperature. When the sintering temperature exceeded 1300 °C, the WC grain size increased significantly with increasing temperature and holding time, and the dominant mechanism for grain growth was grain boundary diffusion. The high densification resulted in a substantial increase in effective grain boundary area, thereby increasing both hardness and fracture toughness of the material. Benefiting from the fine grain strengthening effect of the high-entropy alloys (HEAs) and the excellent wettability of Co, a highly dense cemented carbide material with excellent hardness and fracture toughness is achieved at the sintering temperature of 1300 °C, characterized by a relative density of 99.3 %, a hardness of 2064.9 MPa, and a fracture toughness of 11.5 MPa m−2.

Defect-rich N, S Co-doped porous carbon with hierarchical channel network for ultrafast capacitive deionization

Developing an eco-friendly and effective approach for preparing N, S co-doped hierarchical porous carbons (NSHPC) for capacitive deionization (CDI) is a huge task for desalination. Herein, NSHPCSKK with interconnected hierarchical pore structures, manufactured via self-activation/co-activation of sodium lignosulfonate (SLS) encapsulation using KNO3-KHCO3 activators, inducing N, S co-doping. Different from NSHPCS and NSHPCSK, NSHPCSKK exhibits the highest specific surface area (SBET, 2264.67 m2/g) and a unique hierarchical pore structure (mesoporous volume/pore volume (Vmeso/ Vpore), 0.65). Small-angle X-ray scattering (SAXS) and scanning electron microscopy (SEM) both reveal the complex interconnected pore structure of NSHPCSKK. Regional Raman imaging conjugated with XPS reveals the presence of extensively distributed N, S co-doped defect structures, providing NSHPCSKK with excellent wettability and electrochemical performance. DFT calculations indicate that the N, S co-doping at the defect sites depicts excellent adsorption capability. Eventually, NSHPCSKK acquired an impressive salt adsorption capacity (SAC) of 20.5 mg/g and the highest average salt adsorption rate (ASAR) of 12.1 mg/g/min, indicating its superior desalting performance. In-situ Raman spectroscopy confirms NSHPCSKK’s rapid ion regeneration mechanism. The research introduces a span-new NSHPC synthesis strategy for fabricating advanced NSHPC with rapid desalination response for upgrading CDI desalination.

Morphological Characteristics of W/Cu Composite Nanoparticles with Complex Phase Structure Synthesized via Reactive Radio Frequency (RF) Thermal Plasma

The W/Cu binary system is characterized by its mutual insolubility and excellent wettability, making W/Cu composite materials ideal for managing thermal and electrical properties in electronic components. To optimize material properties, control over the microstructure is crucial, and nanocomposites with uniform dispersion offer significant advantages. In this study, W/Cu composite nanoparticles were synthesized by feeding a blended feedstock of tungsten trioxide (WO3) micro-powder and cupric oxide (CuO) micro-powder into a reactive radio frequency (RF) argon–hydrogen thermal plasma system. Cu-coated W nanocomposite particles were obtained through the vaporization, reduction, and condensation processes. The resulting nanocomposite particles were composed of body-centered cubic (BCC) α-W, A15 β-W, and face-centered cubic (FCC) Cu phases, with a chemical composition closely matching theoretical calculations. The phase evolution and morphological changes of the synthesized particles were analyzed as a function of heat treatment temperatures up to 1000 °C in a reducing atmosphere. Up to 600 °C, the phase composition and morphology remained stable. At 800 °C, localized diffusion and coalescence of Cu led to the formation of particulate Cu, and a significant phase transformation from metastable β-W to α-W was observed. Additionally, extensive Cu segregation due to long-range diffusion resulted in distinct Cu-rich and Cu-depleted regions. In these regions, notable sintering of W particles and the complete disappearance of β-W occurred. The results showed that the temperature-dependent redistribution of Cu plays a crucial role in the phase transformation of W and the morphology of W/Cu composite particles.

Low-tortuosity, high-loading electrodes for fast-charging quasi-solid-state lithium metal batteries

Structural design of electrodes is a widely adopted approach towards enhanced electrochemical performance in various battery systems. However, in quasi-solid-state lithium metal batteries, research has predominantly focused on developing gel polymer electrolytes (GPEs), with limited attention given to utilizing electrodes with specialized structural design. Herein, by exploiting the excellent wettability and permeability of the GPE, high-loading NMC-811 cathodes featuring aligned channels achieved through freeze-casting are integrated with in-situ UV-polymerized poly (butyl acrylate) (PBA). The aligned channels in the freeze-cast electrodes provide low-tortuosity pathways for smooth Li+ transport, facilitating rapid kinetics. Consequently, superior areal capacity can be delivered under high areal current density (e.g. 1 mAh cm−2 at 2 mA cm−2 and 0.7 mAh cm−2 at 3.8 mA cm−2), demonstrating the fast-charging capability of quasi-solid-state lithium metal batteries.

A self-adaption robust superhydrophobic cement mortar for resistance of cold environment

Superhydrophobic coatings have wide range of engineering applications due to its excellent wettability. However, the durability of superhydrophobic coatings is still challenging under complex environments, especially in cold regions. In this study, we prepared a new self-adaption superhydrophobic cement mortar (SSCM) by wettability modified aggregates with polydimethylsiloxane adhesive and silica nanoparticles decorated by 1H,1H,2H,2H-perfluorodecyltriethoxysilane. Subsequently, a series of multi-scale characteristics of the SSCM sample were systematically investigated, including the micro morphology, the chemical compositions, the self-adaption robustness, the anti−/de-icing properties, and the freeze-thaw (F-T) resistance. The results indicate that surface and inside of the SSCM samples exhibit a self-adaption superhydrophobicity with the 150.0° contact angle due to the low surface energy micro/nano structure of wettability modified aggregates. Meanwhile, the SSCM sample shows excellent anti−/de-icing abilities due to the stable rough micro/nano structure under negative-temperature ambient, which can delay the droplet freezing time by 4.3 times than that of the contrast sample. Additionally, the newly exposed section of SSCM sample can still have the self-adaption superhydrophobicity and endow significant F-T resistance even if the surface of SSCM was damaged. Meanwhile, the SSCM sample can improve the F-T resistance by 45 % compared to the contrast sample. This work provides a new strategy to solve the durability limitation of superhydrophobic coating in engineering practice.

In-situ N, P co-doped porous carbon derived from biomass waste for supercapacitors

The development of heteroatom-doped porous carbon derived from biomass waste with high-performance electrodes for supercapacitors has been drawn extensive research. Herein, N, P co-doped porous carbon (NPC) was successfully synthesized using Chinese fir sawdust as a carbon source, NaOH as an activator, urea as a nitrogen source, and melamine phosphate as the phosphorus and nitrogen source by pretreatment with low-temperature NaOH/urea system. The low-temperature pretreatment and melamine phosphate greatly promoted the porous structure and uniform distributions of heteroatom about the NPC. The optimized NPC exhibits high specific surface area (1849 m2/g), hierarchical porous structure with high mesoporosity (87.3 %), appropriate heteroatom content (3.32 at% N, 0.36 at% P), and excellent wettability. This unique facilitates improved electrolyte diffusion efficiency and ion transfer rate. In the three-electrode system, the specific capacitance of the NPC electrode is as high as 260 F/g at 0.5 A/g and remains at 235 F/g at 10 A/g, and the charge transfer resistance is very low (0.08 Ω). In addition, the assembled symmetric supercapacitors deliver an energy density of 15.9 Wh/kg at a power density of 246 W/kg, a long cycling life with 90 % capacitance retention after 5000 cycles. The environment-friendly NPC has a broad development prospect for carbon-based high-performance electrodes for supercapacitors.

Characterization and Performance Evaluation of Liquid Biodegradable Mulch Films and Its Effects on Peanut Cultivation.

With the development of material science and increasing awareness of ecological environmental protection, liquid biodegradable mulch films (LBDMs) have garnered significant public interest. In this research, new LBDMs were developed using hydrophobically modified polymer materials, surfactants, and photosensitive catalysts. Characterization by scanning electron microscopy (SEM) revealed good material compatibility. LBDMs exhibited excellent wettability and degradability, effectively covering soil surfaces and enhancing soil moisture conservation, with a degradation rate of 76.09% after 80 days of burial. The field performance experiment was conducted over two consecutive years, 2021 and 2022, to assess differences in soil temperature and moisture, peanut agronomic traits, pod traits, and yield under four treatments: non-mulching (CK), LBDMs, clear polyethylene mulch films (CPEMs), and black polyethylene mulch films (BPEMs). LBDMs increased soil temperature by 0.56 °C and soil moisture by 19.25%, accelerated the seedling stage by 4-to-6 days, and improved the average emergence rate by 15.91%. Furthermore, LBDMs significantly promoted peanut growth, and it increased yield by 14.34% compared to CK. LBDMs performed comparably to the two types of PE films in maintaining soil conditions and different crop phenotype traits, including plant height, branch number, yield, and quality, and they even outperformed PE films in productivity per plant and 100-kernel weight. These findings suggest that LBDMs are a promising eco-friendly alternative to traditional PE films.

Porous Wood Composite as a Green Approach for Enhancing Electrochemical Performance of Gel Polymer Electrolytes for Supercapacitors.

Delignified wood (DW) is a kind of environment-friendly porous material, and its unique hierarchical orous structure and excellent wettability are conducive to the rapid transfer and storage of ions, which can be used as electrolyte matrix of supercapacitors. In order to solve the deficiency of mechanical properties of DW as electrolyte materials, a novel cross-linked polyurethane (CPU) with high water absorption is designed as a reinforced matrix to improve the mechanical properties of electrolytes while maintaining high ionic conductivity. First, DW is immersed in CPU precursor solution, and the DW/CPU composite (W-CPC) is obtained by thermal crosslinking. Finally, W-CPC is soaked in 1 M LiClO4 aqueous electrolyte to obtain the composite gel polymer electrolyte (W-CPC-GPE). Benefiting from the good hydrophilicity of W-CPC, the anisotropic vertical channels inside the DW, and the synergism of hydrogen bond and covalent bond. The highest ionic conductivity and mechanical strength of W-CPC-GPE are 3.5×10-2 S cm-1 and 0.67 MPa, respectively. The W-CPC-5-G based supercapacitor exhibits a high specific capacitance of 146.52 F g-1 and favorable capacitance retention rate of 90.7 % after 5000 cycles. The results show that compounding with DW is an efficient and green way to develop high-performance gel polymer electrolytes for supercapacitors.

Two-dimensional Cu2N–A high-performance anode material for ion batteries with excellent electrical conductivity and electrolyte wettability

Determining suitable anode materials is crucial in the advancement of lithium-ion and sodium-ion battery technologies. We propose that the two-dimensional (2D) material Cu2N holds promise as a viable anode candidate. The Cu2N monolayer exhibits a stable checkerboard lattice crystal structure, ensuring structural integrity. Its excellent metallic electronic structure facilitates efficient conductivity during battery operation. We have observed that Li/Na ions can chemically bond to Cu2N substrates via specific charge exchange mechanisms. Moreover, the Cu2N monolayer demonstrates favorable wettability and compatibility with common electrolytes used in lithium-ion and sodium-ion batteries, including solvent molecules and metal salts. Our findings indicate that the Li/Na storage capacity of the Cu2N monolayer reaches approximately 760/760 mAh/g, surpassing that of graphite anodes significantly. Notably, the Li/Na diffusion barrier on the Cu2N monolayer is merely 5/13 meV, lower than that of most other 2D anode materials. Our results underscore the potential of the Cu2N monolayer as an outstanding electrode material, offering high storage capacity, rapid charge/discharge rates, and favorable wettability with electrolytes.

Biobased Polybutyrolactam Nanofiber with Excellent Biodegradability and Cell Growth for Sustainable Healthcare Textiles.

The white pollution caused by unsustainable materials is a significant challenge around the globe. Here, a novel and fully biobased polybutyrolactam (PBY) nanofiber membrane was fabricated via the electrospinning method. As-spun PBY nanofiber membranes have good thermal stability, high porosity of up to 71.94%, and excellent wetting behavior. The biodegradability in soil, UV aging irradiation, and seawater was investigated. The PBY nanofiber membrane is almost completely degraded in the soil within 80 days, showing excellent degradability. More interestingly, γ-aminobutyric acid, as a healthcare agent with intrinsic hypotensive, tranquilizing, diuretic, and antidiabetic efficacy, can be detected in the degradation intermediates. In addition, the PBY nanofiber membrane also exhibits antibacterial ability against Escherichia coli. As a fully biomass-derived material, the PBY membrane has excellent biodegradable performance in various environments as well as negligible cytotoxicity and commendable cell proliferation. Our PBY nanofiber membrane shows great potential as biodegradable packaging and in vitro healthcare materials.

Economical and rapid mechanochemical synthesis of porous organic adsorbents with high hydrophilicity for ultra-fast removal of organic micro-pollutants from water

Various porous adsorbent materials have shown excellent adsorption performance for the removal of organic micro-pollutants in water. However, the practical application was hindered by the high cost or slow adsorption kinetics for most of porous adsorbents. Therefore, it is of great significance to develop economic adsorbent materials with characteristic like low-cost, easier preparation method, excellent adsorption kinetics etc.Herein, based on the Friedel-Crafts alkylation reaction, we reported three novel hydrophilic organic porous adsorbent frameworks (PAF-210, PAF-211 and PAF-212) with high Brunauer-Emmet-Teller (BET) surface area (956 ∼ 1384 m2/g) for phenolic micro-pollutants (bisphenol A (BPA), 2,4-dichlorophenol (2,4-DCP) and 2-naphthol (2-NO)) adsorption in water, which were prepared by using cheap trimethyl orthoformate (TMOF) as crosslinker and one-step simple ball milling synthetic method under room temperature within 15 min. Rich oxygen content promotes the resulting polymers to possess excellent hydrophilicity and wettability through water vapor adsorption and water contact angle analysis. The excellent hydrophilicity and proper porous properties made the resulting frameworks suitable as porous organic adsorbents to rapidly remove organic phenolic micro-pollutants from water. Among the resulting polymers, the PAF-210 exhibited ultra-fast adsorption (>94.0 % within 5 s), ultra-rapid adsorption kinetics with pseudo-second-order rate constants (K2, up to 7.72g/mg min−1 for 2,4-DCP), high pollutant adsorption capacity (up to 867.03 mg g−1 for BPA) and excellent recyclability (10 cycles with slight loss in adsorption capacity) through systematically characterization. The adsorption performances of PAF-210 are much better than these of the commercial activated carbons and β-cyclodextrin-based porous adsorbents (K2 = 1.50g/mg min−1 for P-CDP) etc. The favorable hydrophilicity, surface wettability, and adsorption performance of PAF-210 were significantly better than the comparative material constructed by using benzene and formaldehyde dimethyl acetal (FDA) through conventional thermal synthetic method, which is a very classic synthesis strategy in the field of porous materials. More importantly, the PAF-210 exhibited relatively superior adsorption performance on BPA, and it still presented excellent adsorption performance (removal efficiency ≥ 96.8 % within 5 s after 10 cycles) even at the safe range of BPA quantified in drinking water (BPA≤10 μg L−1, Standards for drinking water quality, GB5749-2022, China). XPS analysis and theoretical simulations proved that the excellent adsorption performance and ultra-fast adsorption rate stem from interactions including π-π interactions, hydrogen bonding and van der Waals interactions between PAF-210 and micro-pollutants.

Dual-stimuli-responsive silica-based emamectin benzoate nanodelivery system for effective control of Spodoptera frugiperda and safety assessment toward Microplitis manilae

The utilization of highly efficient and ecofriendly stimulus-responsive delivery systems for pesticides represents a powerful strategy for enhancing their efficacy and environmental safety. In this study, the application of emamectin benzoate (EB)-loaded amino-functionalized rough mesoporous silica (KMSNs)@poly(glycidyl methacrylate-co-acrylic acid) (PMA) composites (KMSNs@PMA@EB, 6.52 % loading capacity for EB) to control efficacy for Spodoptera frugiperda was investigated in detail. The results showed that, KMSNs@PMA@EB rapidly released EB under acidic and high-temperature conditions. compared with EB and commercial formulations, a solution of KMSNs@PMA@EB with the agricultural organosilicon additive exhibited excellent wetting. Compared with MSNs, KMSNs@PMA significantly enhanced the effective deposition. Moreover, the photostability of KMSNs@PMA@EB was improved by 1.87-fold and 2.25-fold compared to EB and an EB suspension concentrate (EB SC). S. frugiperda larvae preferred corn leaves with low concentrations (0.125 mg/L) of KMSNs@PMA@EB than EB-treated. Bioassays revealed that KMSNs@PMA@EB maintained > 37 % control efficiency after 21 d of spraying, KMSNs@PMA@EB exhibited significantly greater insecticidal activity and persistence against S. frugiperda than commercial formulations. After 21 days of application, the final deposition rates of KMSNs@PMA@EB were lower than the maximum residual limit of EB, spraying KMSNs@PMA@EB has a lower impact on corn plants. Furthermore, biological safety assessments confirmed that KMSNs@PMA@EB did not affect the maize seed germination and growth and posed a low risk to Microplitis manilae. Those results highlight that the advantages of KMSNs@PMA@EB nanoparticles multidimensional enhancement of pesticide efficacy, persistence, and safety to parasitic wasps and has great potential to be used in pest control combining parasitoid and nanopesticides.

Polyetheramine enhanced biosurfactant/biopolymer flooding for enhanced oil recovery

The application of conventional alkali, surfactant and polymer in alkali/surfactant/polymer (ASP) flooding has exposed the inherent shortcomings of pollution and damage to reservoirs. Hence, finding new environmentally friendly alternatives is essential for the sustainable development of ASP flooding. In this paper, we proposed a novel ternary combination utilizing organic alkali polyetheramine, biosurfactant, and biopolymer as alternative chemical agents for ASP flooding. Specifically, the ASP system composed of polyetheramine D230, biosurfactant sophorolipid (SL) and biopolymer welan gum (WLG) exhibited excellent potential in improving oil recovery. The interfacial tension measurements proved that D230 could react with organic acids in crude oil to generate surface-active soaps, which cooperated with SL to reduce the oil–water interfacial tension to 10−2 mN/m. The rheological measurements demonstrated that the addition of D230 could increase the viscosity of low concentration WLG solution, but this phenomenon gradually disappeared with the rise of WLG concentration. Even at higher WLG concentration, D230 only caused a slight decrease in system viscosity, which facilitated the improvement of sweep efficiency. Emulsification and contact angle measurements indicated that D230/SL blend had outstanding emulsifying ability and successfully altered the quartz surface from oil-wet to water-wet. Core flooding experiments and micromodel experiments showed that the D230/SL/WLG system significantly enhanced oil recovery by 22.66 %, which was attributed to the high viscosity, low interfacial tension, excellent wettability reversal and emulsifying abilities of the system. The economic benefit assessment indicated that this ASP system has the potential to be economic, rendering it profitable even during periods of low oil prices. Furthermore, the EC50 value of 52,600 mg/L for D230/SL/WLG demonstrated its environmental friendliness.

Research on the influence of dynamic contact angle of mercury meniscus on the interpretation of rock pore throat radius in mercury intrusion experiments

Addressing the lack of measurement methods for dynamic contact angles of mercury meniscus in mercury intrusion porosimetry experiments and the unclear understanding of the impact of dynamic contact angles on the interpretation of pore throat radius in rocks, a new type of closed mercury intrusion characteristic curve (O-R curve) is constructed utilizing the withdrawal curve O and the secondary injection curve R obtained from the experiments. Based on the excellent wetting and de-wetting correlation characteristics at the equal mercury saturation points on this curve, a method for measuring the dynamic contact angles of mercury meniscus (O-R loop method) is established. Taking the Chang 63 tight oil reservoir samples from the Nanliang Oilfield in the Ordos Basin of China as an example, this method is applied to investigate the dynamic contact angles of mercury meniscus in mercury intrusion porosimetry experiments and the impact on the interpretation of pore throat radius in rocks. The results indicate that the dynamic contact angles of mercury meniscus changes significantly during the experiments, which cannot be ignored. And the smaller pore throats lead to more severe deformation of mercury meniscus, resulting in higher wetting resistance coefficients and hysteresis angles. Calculations reveal that the pore throat radius interpreted using the modified Washburn equation (which adopts dynamic contact angles) are generally larger than those interpreted using the conventional Washburn equation (which adopts static contact angles), with relative errors ranging from 12.2% to 54.7%. The smaller the pore throats, the larger the relative errors. The analysis shows that the conventional Washburn equation significantly underestimates the reservoir pore throat radius due to the neglect of the dynamic contact angle, while the modified Washburn equation provides more accurate interpretation. Overall, this research provides a method for calculating the dynamic contact angle in mercury intrusion porosimetry experiments and has important reference significance for the accurate interpretation of rock pore throat radius.

Development of pectin/chitosan-based electrospun biomimetic nanofiber membranes loaded with dihydromyricetin inclusion complexes for wound healing application

Accidents and surgical procedures inevitably lead to wounds, presenting clinical challenges such as inflammation and microbial infections that impede the wound-healing process. This study aimed to address these challenges by developing a series of novel wound dressings known as electrospun biomimetic nanofiber membranes. These membranes were prepared using electrostatic spinning technique, incorporating hydroxypropyl-β-cyclodextrin/dihydromyricetin inclusion complexes. The prepared electrospun biomimetic nanofiber membranes exhibited randomly arranged fiber morphology with average fiber diameters ranging from 200 to 400 nm, resembling the collagen fibers in the native skin. These membranes demonstrated excellent biocompatibility, hemocompatibility, surface hydrophilicity, and wettability, while also releasing dihydromyricetin in a sustained manner. In vitro testing revealed that these membranes, loaded with hydroxypropyl-β-cyclodextrin/dihydromyricetin inclusion complexes, displayed higher antioxidant potential and inhibitory effects against Staphylococcus aureus and Escherichia coli. Furthermore, these membranes significantly reduced the M1 phenotypic transition in RAW264.7 cells, even when stimulated by lipopolysaccharides, effectively restoring M2 polarization, thereby shortening the inflammatory period. Additionally, the in vivo wound healing effects of these membranes were validated. In conclusion, this study introduces a promising nanofiber membrane with diverse biological properties that holds promise for addressing various crucial aspects of the wound-healing process.

Polyetherketoneketone/carbon fiber composites with an amorphous interface prepared by solution impregnation

Interfacial adhesion between carbon fibers (CF) and polyetherketoneketone (PEKK) is a key factor that affects the mechanical performances of their composites. It is therefore of great importance to impregnate the CF bundles with PEKK as efficiently as possible. We report that PEKK with a good dispersion in a mixed solution of 4-chlorophenol and 1,2-dichloroethane can be introduced onto CF surfaces by solution impregnation and curing at 280, 320, 340 and 360 °C. The excellent wettability or infiltration of the PEKK solution guarantees a full covering and its tight binding to CFs, making it possible to evaluate the interfacial shear strength (IFSS) with the microdroplet method. The interior of the CF bundles is completely and uniformly filled with PEKK by solution impregnation, leading to a high interlaminar shear strength (ILSS). The maximum IFSS and ILSS reached 107.8 and 99.3 MPa, respectively. Such superior shear properties are ascribed to the formation of amorphous PEKK in the small spaces between CFs.