Mixed Solution Research Articles

Graphene oxide/polydopamine interface co-reinforced carbon paper: With comprehensive mechanical properties, electrical conductivity and air permeability

Proton Exchange Membrane Fuel Cell ( PEMFC) are characterised by their cleanliness, efficiency and lack of pollution. Carbon paper, the fundamental material for constructing gas-diffusion layer (GDL), plays a crucial role in electron transmission, supporting the electrode structure, and proton transport. However, the traditional carbon paper for GDL significantly limits the large-scale commercial application of PEMFC due to its low mechanical strength and poor conductivity. Based on this, in this paper, polydopamine is used to modify primary carbon fiber paper, a homogeneous mixed solution of graphene oxide and phenolic resin is used as the impregnating agent, and the effects of different GO concentrations on the properties of carbon paper are investigated. The results show that the graphitization degree and mechanical properties of carbon paper are improved with the increase of GO concentration. When the content of polydopamine is 2 g/L and the concentration of GO is 0.5 wt%, the carbon paper exhibits optimal performance. The air permeability of carbon paper is 12.18 L/min, the resistivity is 13.5 mΩ·cm, and the tensile strength is 19.3 MPa. This study provides a simple method for preparing highly breathable and highly conductive carbon paper, offering a reference for achieving low-cost and high-performance carbon paper production, and facilitating the large-scale commercial production of carbon paper.

Facile synthesis of triple‐network organo‐hydrogel for all‐temperature flexible supercapacitors

AbstractA new triple‐network organo‐hydrogel with high anti‐freezing and thermally‐stable performance is prepared for application in all‐temperature flexible supercapacitor. It is composed of boric acid/graphene/polyvinyl alcohol matrix and H2SO4/dimethyl sulfoxide mixing solution. The incorporation of graphene and boric acid into polymer matrix can improve thermal stability and ionic conductivity of organo‐hydrogel. The H2SO4 and dimethyl sulfoxide are key roles for improving anti‐freezing of organo‐hydrogel. The organo‐hydrogel exhibits high ionic conductivity of 1.6 and 3.1 S/m at −80 and 90°C, respectively. As a result, the assembled supercapacitor delivers a high capacitance retention of 84.5% and 113.3% at ultra‐low temperature (−80.0°C) and high temperature (90.0°C), respectively. The work provides a new route to design and prepare flexible supercapacitor with wide temperature range.

Research on CO2 capture performance and reaction mechanism using a novel low energy consumption and high cyclic performance absorbent for onboard application

High desorption energy consumption and low cyclic loading are critical issues limiting the application of onboard carbon capture (OCC) systems. In this study, a tetraethylenepentamine (TEPA) and 2–amino–2–methyl–1–propanol (AMP) mixed amine solvent with low desorption energy consumption and high CO2 cyclic loading, suitable for the operational environment of OCC systems, has been proposed. Detailed research was conducted on the capture performance and mechanism of the TEPA + AMP mixed amine solvent. The 0.25M TEPA+0.75M AMP mixed amine solvent exhibited the best performance, with an 86.5% increase in CO2 loading, a 214% increase in single–cycle CO2 loading, a 236% increase in CO2 loading after four cycles compared to monoethanolamine (MEA), and a 20.76% reduction in desorption energy consumption. In addition, to address the challenge of applying polyamine mixed solutions in the simulation studies of OCC systems, the capture mechanism was analyzed using density functional theory (DFT) calculations and nuclear magnetic resonance (NMR) characterization. The results indicated that increasing AMP promoted HCO3– formation in the TEPA + AMP mixed amine solvent. Since HCO3– decomposed more easily than carbamate, it reduced desorption energy consumption. However, an excess of AMP inhibited the absorption rate of TEPA, affecting the absorption capacity. Increasing the concentration of TEPA enhanced the amine concentration in the absorbent and improved the absorption performance. Nevertheless, excessive TEPA caused AMP to participate only in deprotonation reactions, which was not conducive to reducing desorption energy consumption.

Environmentally Benign High‐Performance Composites‐Based Hybrid Microcrystalline Cellulose/Graphene Oxide

ABSTRACTA novel silane functionalization prepared by a solution mixing approach of epoxy composites filled with eco‐friendly reinforcement filler, that is, graphene oxide (GO) and microcrystalline cellulose (MCC). The developed composites were subjected to comprehensive analysis using various characterization techniques, encompassing mechanical testing, water absorption analysis, thermal stability assessment, and scanning electron microscopy (SEM). The tensile strength and Young's Modulus of the epoxy composite filled with 1.0 wt.% of GO (EGO1.0) demonstrated the highest value viz. 29.83 MPa and 1991.71 MPa, respectively, when compared to neat epoxy composite (E0). Meanwhile, the thermal gravimetry analysis (TGA) studies, particularly char yield, highlight improvements in the thermal stability of the EGO2.5 composite, that is, 23.39% representing a 33.73% increment compared to the E0 composite. The synergistic effect of hybrid filler, achieved by a combination of micro and nanoparticle fillers within an epoxy matrix, was investigated as a virtuous alternative to the conventional epoxy nanocomposites. A uniform dispersion of GO on the MCC surface leads to significant improvements in the mechanical properties and thermal stability of the epoxy‐reinforced composite. The maximum tensile strength, Young's Modulus, and break strain of 39.77 MPa, 2591.27 MPa, and 2.90%, respectively, were observed for the modified EGO1.0MCC1.5 composite. The synergistic effect of hybrid eco‐friendly reinforcement fillers (GO/MCC) and a strong interfacial adhesion between the matrix and filler reduces the formation of defects, thereby resulting in good stress transfer from matrix to fillers.

Construction of Mo/S/Ag Cluster Complexes from Dinuclear Molybdenum Precursors [R4N]2[(edt)2Mo2S2(μ‐S)2] (R = Et, nPr; edt = −SCH2CH2S−)

AbstractWe have demonstrated that complexes [(edt)2Mo2O2(μ‐S)2Ag2(dppm)2]·4CH3OH·DMF (2, edt = 1,2‐ethanedithiolate dianion, dppm = bis(diphenylphosphino)methane, DMF = N,N‐dimethylformamide) and [(μ‐Cl)2Ag4(μ3‐Cl)2(dppm)2]·4DMF (3), were generated by combining a dinuclear molybdenum precursor [Et4N]2[(edt)2Mo2S2(μ‐S)2] (1a) with two equimolar AgCl and dppm in a CH3OH‐DMF mixed solution. Treatment of complex 1a with one equimolar AgCl and DPEPhos in CH3OH and DMF mixed solutions, producing complex [Et4N][(edt)2Mo2S2(μ‐S)2Ag(DPEPhos)]·CH3OH (4, DPEPhos = bis(2‐diphenylphosphinophenyl)ether). Treatment of complex [nPr4N]2[(edt)2Mo2S2(μ‐S)2] (1b) with AgBr in acetonitrile followed by addition of (NH4)2S produced a dodecanuclear Mo–Ag–S cage cluster [nPr4N]2[{Mo2Ag2S2O2(edt)2}3(μ6‐S)]·1.5CH3CN (5). Complexes 2−5 have been characterized by infrared(IR), 1H NMR, UV‐vis, and fluorescence spectroscopies. Moreover, molecular structures of complexes 2−5 have been established by single‐crystal X‐ray crystallography.

3D-printed poly(p-dioxanone)/graphene oxide composite bioresorbable stents for congenital heart disease treatment

Bioresorbable stents (BRSs) offer significant advantages in treating congenital heart disease-related vascular stenoses, especially for pediatric patients. However, the insufficient mechanical performance of polymeric BRSs remains a critical challenge. In this study, Poly(p-dioxanone) (PPDO) was incorporated with graphene oxide (GO) for the first time to improve both mechanical properties and biocompatibility. PPDO/GO composites with varying GO contents were fabricated via solution mixing and solvent casting, and tensile tests revealed that lower GO content levels (0.2% and 0.5%) significantly improved the Young’s modulus, tensile strength, and elongation at break of PPDO due to hydrogen bonding and increased degree of crystallinity. 3D-printed PPDO/GO sliding-lock stents with optimal GO contents were fabricated by fused deposition modeling and demonstrated superior compression force compared to pristine PPDO stents. In vitro hemocompatibility and cytocompatibility assessments showed that 3D-printed PPDO/GO stents exhibited low hemolysis rate, reduced platelet adhesion, and enhanced adhesion and proliferation of endothelial cells. In vivo evaluation further demonstrated improved endothelialization in rat abdominal aortas implanted with 3D-printed PPDO/GO filaments for 4 weeks. Overall, PPDO/0.5%GO exhibited superior performance in compression force, hemocompatibility, cytocompatibility, and in vivo endothelialization. This study, for the first time, combines PPDO with GO and explains the mechanism of the enhanced mechanical properties of PPDO/GO composite material. Using 3D printing, PPDO/GO BRS with improved compression performance and biocompatibility were developed, highlighting its potential value for treating pediatric patients with CHD-related vascular stenoses.

Application of the Thermal Analysis of Frozen Aqueous Solutions to Assess the Miscibility of Hyaluronic Acid and Polymers Used for Dissolving Microneedles.

Background: The combination of multiple polymers is anticipated to serve as a means to diversify the physical properties and functionalities of dissolving microneedles. The mixing state of components is considered as a crucial factor in determining their suitability. Objectives: The purpose of this study was to elucidate whether thermal analysis of frozen aqueous solutions can appropriately predict the miscibility of hyaluronic acid (HA) and other polymers used for dissolving microneedles prepared by a micromolding method. Methods: Aliquots of aqueous polymer solutions were applied for thermal analysis by heating the samples from -70 °C at 5 °C/min to obtain the transition temperature of amorphous polymers and/or the crystallization/melting peaks of polymers (e.g., polyethylene glycol (PEG)). Films and dissolving microneedles were prepared by air-drying of the aqueous polymer solutions to assess the polymer miscibility in the solids. Results: The frozen aqueous single-solute HA solutions exhibited a clear Tg' (the glass transition temperature of maximally freeze-concentrated solutes) at approximately -20 °C. The combination of HA with several polymers (e.g., dextran FP40, DEAE-dextran, dextran sulfate, and gelatin) showed a single Tg' transition at temperatures that shifted according to their mass ratio, which strongly suggested the mixing of the freeze-concentrated solutes. By contrast, the observation of two Tg' transitions in a scan strongly suggested the separation of HA and polyvinylpyrrolidone (PVP) or HA and polyacrylic acid (PAA) into different freeze-concentrated phases, each of which was rich in an amorphous polymer. The combination of HA and PEG exhibited the individual physical changes of the polymers. The polymer combinations that showed phase separation in the frozen solution formed opaque films and microneedles upon their preparation by air-drying. Coacervation occurring in certain polymer combinations was also suggested as a factor contributing to the formation of cloudy films. Conclusions: Freezing aqueous polymer solutions creates a highly concentrated polymer environment that mimics the matrix of dissolving microneedles prepared through air drying. This study demonstrated that thermal analysis of the frozen solution offers insights into the mixing state of condensed polymers, which can be useful for predicting the physical properties of microneedles.

Ultrasonic-aided preparation of poly(vanillin-co-thiophene)/green Fe₃O₄ nanocomposites via solution mixing for methyl orange adsorption and antibacterial applications

This work describes the preparation of novel nanocomposite materials comprising a newly synthesized semiconducting copolymer, poly(vanillin-co-thiophene) (PVTH), blended with different weight proportions (3 %, 6 %, and 9 % by weight) of greenly synthesized magnetite nanoparticles (GFe3O4 MNPs) via solution mixing, assisted by ultrasonic irradiation. PVTH copolymer was synthesized through the polycondensation of vanillin, a bioderived aldehyde, and thiophene, catalyzed by sulfuric acid. GFe3O4 MNPs were prepared via the coprecipitation method with mint extract as an environmentally friendly stabilizer. The physicochemical properties of the prepared samples were investigated by 1H NMR, 13C NMR, FTIR, XRD, UV–vis, TGA, FE-SEM/Eds, AFM, VSM, tauc plot method and the four-points probe measurement. The samples were evaluated for two applications: methyl orange (MO) adsorption from aqueous solutions and antibacterial activities against Gram-negative (Escherichia coli and Pseudomonas aeruginosa) and Gram-positive (Staphylococcus aureus and Bacillus) bacterial strains. The results showed that ultrasound irradiation facilitated the easy preparation of well-dispersed and homogeneous nanocomposites with combined semiconducting and magnetic properties and improved thermal stability compared to the parent PVTH. The most effective nanocomposite for MO removal was the sample containing 9 % GFe3O4 MNPs, whose adsorption behavior followed pseudo-second-order kinetics and Freundlich isotherm. Its maximum adsorption capacity was 103.79 mg g−1. In addition, all samples showed antibacterial action against the tested bacterial strains, with PVTH showing the highest efficacy, followed by PVTH/GFe3O4 nanocomposites.

Sustainable poultry practices: integrating green light interventions to control pecking in chicken

BackgroundThe present study aimed to investigate the impact of the light-emitting diode (LED) green light alone or in combination with melatonin on pecking-related hormone regulation during incubation under normal and under hormonal stress conditions in breeder eggs. This study was divided into 2 experiments: In the first experiment effect of LED green light incubation on pecking-related hormones under normal conditions, on Hy-line brown (low pecking phenotype) and Roman pink (high pecking phenotype) eggs were tested. The 296 eggs of each strain were divided into two groups: LED green light incubation and dark incubation (control), each containing four replicates (37 eggs/replicate). The second experiment was conducted to evaluate the effect of LED green light incubation alone or in combination with melatonin under hormonal stress conditions on Roman pink eggs. A total of 704 Roman pink eggs were taken and divided into four groups, each consisting of 176 eggs. Each group was further divided into 2 subgroups, LED green light-regulated incubation and dark incubation with 88 eggs per subgroup, having 4 replicates of 22 eggs each. The groups were as follows: corticosterone solution injection (CI), corticosterone + melatonin mixed solution injection (CMI), Phosphate buffer solution injection (PI), and no injection (UI).ResultsResults of the first experiment revealed a higher level of serotonin hormone and lower corticosterone hormone in Hy-Line brown embryos compared to Roman pink embryos during dark incubation. The LED green light incubation significantly (P < 0.05) increased the level of 5-HT while decreasing the CORT level in Roman pink embryos indicating its regulatory effect on pecking-related hormones. Results of the second experiment showed that LED green light incubation significantly (P < 0.05) alleviated the CORT-induced hyperactivity of plasma 5-HT in Roman pink embryos. Furthermore, Melatonin (MLT) injection and LED green light together significantly (P < 0.05) reduced the hormonal stress caused by corticosterone injection in the eggs.ConclusionsOverall, the LED green light regulatory incubation demonstrated a regulatory effect on hormones that influence pecking habits. Additionally, when coupled with MLT injection, it synergistically mitigated hormonal stress in the embryos. So, LED green light incubation emerged as a novel method to reduce the damaging pecking habits of poultry birds.

Exploring the Electrochemical Superiority of V2O5/TiO2@Ti3C2-MXene Hybrid Nanostructures for Enhanced Lithium-Ion Battery Performance.

The use of vanadium(V)-based materials as electrode materials in electrochemical energy storage (EES) devices is promising due to their structural and chemical variety, abundance, and low cost. V-based materials with a layered structure and high multielectron transfer in the redox reaction have been actively explored for energy storage. Our current work presents the structural and electrochemical properties of a vanadium-based composite with TiO2@Ti3C2 MXene, referred to as VM. This composite is obtained through the in situ thermal decomposition of the VO2(OH)/Ti3C2mixture, which is achieved by solution mixing and drying. The material structure is confirmed using various characterization tools, which establish an orthorhombic V2O5 nanostructure compositing with nanocrystalline TiO2@Ti3C2. VM with 5 wt % MXene, referred to as VM5, can achieve 460 mAhg-1 at a current density of 0.1 Ag1- and 290 mAhg-1 at 1 Ag1-, with an average coulombic efficiency of 98.5%. The presence of the V2O5/TiO2 (nanocrystals) heterojunction attached with Ti3C2 sheets contributed to reduced charge transfer resistance. The cyclic stability shows a capacity retention of 62% over 500 cycles at 1 Ag1- (4C rate, where 1C equals 0.25 Ag1-) with a 0.22 capacity drop with each cycle. Dunn's approach to examining the charge storage mechanism demonstrates 72% contribution of the surface-dominant capacitive process and 28% of the diffusion-controlled intercalation process at 0.4 mVs-1, suggesting a potential high-performance pseudocapacitive hybrid electrode material for lithium-ion batteries.

Fluoride-Treated Nano-HZSM-5 Zeolite as a Highly Stable Catalyst for the Conversion of Bioethanol to Propylene.

Fluoride treatment of ZSM-5 zeolite can effectively adjust surface acidity and generate a secondary pore structure. In this study, a series of modified nano-HZSM-5 zeolites were prepared by NH4F-HF mixed solution treatment and applied to the selective conversion of bioethanol to propylene at 500 °C, atmospheric pressure, and a WHSV of 10 h-1. The results showed that NH4F-HF modification weakened the surface acidity of nano-HZSM-5 zeolites, thus inhibiting coke formation. Additionally, the mesopores in the nano-HZSM-5 zeolites increased after NH4F-HF treatment, thereby enhancing the mass transfer rate and improving the coke-resistance ability. The NH4F-HF mixed solution modification significantly improved the stability of nano-HZSM-5 zeolites in catalyzing bioethanol to propylene and greatly extended the working life of nano-HZSM-5 zeolites. It can be seen from the characterization of the deactivated catalysts that coke deposition and weakening of acidity may be the key factors for catalyst deactivation.

Construction of mixed gels of yolk granules and salted ovalbumin driven by pH: phase behavior and calcium bioaccessibility

Mixed gels of egg yolk granules (EYGs) and salted ovalbumin (SO) with different pH values were constructed to design gels of great quality and nutritional properties. However, the formation and dietary properties of mixed gels may be affected by the phase behavior of the mixed protein solution. In this study, the pH was adjusted from 3.0 to 8.0 to tune phase behavior of mixed protein solution before heating. The results demonstrated the presence of a collapsed gel and a dense phase network at pH 3.0 caused by phase separation. As the pH increased and phase separation disappeared, the EYGs-SO gel network showed a filling network structure and then changed to a loose interpenetrating network gel structure with a decreased fractal dimension (from 2.94% to 2.89%). The interpenetrating network improved gel hardness and water-holding capacity. During gelation, the phase separation reduced the gelation transition temperature. The main forces that support EYGs-SO gel were hydrogen and disulfide bonds. Moreover, EYGs-SO showed greater calcium bioaccessibility (7.85%–8.08%) at pH 3.0, 4.0, and 5.0. In summary, the phase behavior in mixed solution modulates the gelation of mixed gels. The construction of mixed gels also provides ideas and strategies for the value-added utilization of salted egg whites.

A 3D printed dual screen-printed electrode separation device for twin electrochemical mini-cell establishment.

We describe a tiny 3D-printed polymethyl-methacrylate-based plastic sleeve that houses two disposable screen-printed electrodes (SPE) and enables each of the working electrodes (WEs) to work independently, on a different side of a thin barrier, in its own electrochemical (EC) mini-cell, while the SPE counter and reference units are shared for electroanalysis. Optical and EC performance tests proved that the plastic divider between WE1 and WE2 efficiently inhibited solution mixing between the mini-cells. The two neighboring, independently operating mini-cells enabled matched differential measurements in the same sample solution, a tactic designed for elimination of electrochemical interference in complex samples. In a proof-of-principle glucose biosensor trial, a glucose oxidase-modified WE2 and an unmodified WE1 delivered the EC data for the removal of anodic ascorbic acid (AA) interference simply by subtracting the WE1 (background) current from the analyte-specific WE2 current (from buffered sample solution supplemented with glucose/AA), at an anodic H2O2 detection potential of +1 V. The microfabricated SPE accessory is cheap and easy to make and use. For the many dual electrode SPE strips on the market for multiple analytical targets the new device widens the options for their exploitation in assays of biological and environmental samples with complex matrix compositions and significant risks of interference.

Preparation and Characterization of Black Phosphene/Titanium Dioxide Composite Nanomaterials by Liquid-Stripping and Solution Mixing Method

In this study, black phosphorus (BP) was prepared via the high-energy ball milling method, and two-dimensional (2D) BP was further fabricated using the liquid-phase stripping approach. Nano TiO2 was synthesized via the sol-gel method, and it was combined with black phosphene through N, N-dimethylformamide (DMF) medium by a straightforward solution mixing process to produce BP/ TiO2 composite photocatalyst. Subsequently, spectrophotometric analysis, X-ray diffraction (XRD), and high-resolution transmission electron microscopy (HRTEM) were conducted. The band gap of BP was calculated using the Tauc plot method. The results revealed that the values are 1.06 eV and 1.23 eV, corresponding to the band gap emissions of four-and three-layer BP band gap emission, indicating the successful preparation of few layers of black phosphorus. The HRTEM analysis demonstrated that the BP/ TiO2 composite photocatalyst formed a relatively stable crystalline state.

Design of a mixed robotic machining system and its application in support removal from metal additive manufactured thin-wall parts

Robotic machining could provide a solution for removing supports from metal additive manufactured workpieces, replacing labor-intensive work. However, the robot’s intrinsic weaknesses of low positioning accuracy and structural rigidity primarily restrict its applications. Improving the accuracy of robotic machining remains an unresolved issue. A mixed solution is proposed, in which a portable CNC machine with the capability of visual feature recognition is equipped with a universal industrial robot. The robot implements positioning motions in a large space, while the portable CNC fulfills accurate machining motions on a local feature of the workpiece. A sizeable weight of the portable CNC exerts a moderate load on the industrial robot’s joints, increasing joint stiffness. The mixed machining system exhibits high accuracy and stiffness when milling a steel/titanium alloy workpiece, achieving tolerances up to ±0.04 mm on a 60×80 mm U-shaped path without exciting any structural vibration modes. When the dimension of the workpiece exceeds the machining range of the portable CNC, a combined algorithm of coarse-fine registration based visual identification and robot error compensation is designed to align the spatial coordinates of the machining motion with that of the positioning motion, thereby extending the machining range with high accuracy. Through the proposed mixed robot machining method, experiments of doubling the machining range have been done to verify that the mixed machining robotic system is able to slot a 550 mm-long path with accuracy of ±0.1 mm. Furthermore, the mixed robotic machining system is applied to recognize and remove multiple supports of lattices, grids and ribs from a titanium-alloy additive manufactured thin-wall workpiece with high accuracy and high efficiency.

Nanodiamond Nano-Reinforcements in Thermoplastic (Polyamide, Polyimide, Polystyrene) Nanocomposites—Essential Characteristics and Technicalities

Nanodiamonds are unique spherical carbon nano-entities having the advantages of very high surface area and high optical, thermal, wear and strength characteristics. Like other carbonaceous nanoparticles (like fullerene, graphene or carbon nanotube), nanodiamond nano-reinforcements have been investigated for the significant types of polymeric matrices (such as thermosets, thermoplastics, rubbers) nanocomposites. Consequently, this overview was planned to systematically describe the current scientific status of the nanodiamonds reinforced thermoplastic nanomaterials. In this regard, polyamide/nanodiamonds, polyimide/nanodiamonds and polystyrene/nanodiamonds nanocomposites have been fabricated using the facile solution, in-situ and melt mixing techniques. We suggest that including nanodiamonds in polyamides and polyimides increased their engineering characteristics, like mechanical properties and thermal stability, of the resulting nanocomposites due to a distinct interface formation and their compatibilization effects toward these matrices. Correspondingly, including nanodiamonds in polystyrene has been observed to increase the intrinsically low strength/toughness features of this polymer. Predominantly, nano-reinforcement and miscibility effects of the nanodiamonds with the polystyrene and their mutual matrix-nanofiller synergies were responsible to improve the overall microstructural and physical properties of the resulting nanocomposites. As per our analysis, the research reports so far on the important categories of the nanodiamonds reinforced thermoplastic matrix nanocomposites have shown important technical applications in the fields of high-tech coatings, membranes and energy devices.

Complex Formation of Gold Nanoparticles with Collagen in Aqueous Media Studied by X-ray Scattering and Absorption Spectroscopy.

Small-angle X-ray scattering and UV-vis absorption measurements were performed on mixed solutions of gold nanoparticles (AuNPs) and atelocollagen (AC), triple-helical collagen without telopeptide, in acetate buffer at pH 4 under different temperature conditions, i.e., preparation temperature Tprep and measurement temperature Tmeas. Due to the significantly higher electron density of gold than that of AC, the structure factor S(q) of AuNPs is readily estimated from the scattering intensities of AuNP-only and mixed solutions. The resulting S(q) profile for the mixed solution indicated significant attractive interactions, especially for the smaller AuNPs. Therefore, the sticky sphere model was applied to analyze S(q) to determine the interaction parameters at different Tprep and Tmeas. The attractive interactions between AuNPs were higher at higher Tprep, suggesting that single-chain AC tends to make the interactions between AuNPs more attractive than those for triple-helical AC. Complex formation was also detected by the aggregation-induced surface plasmon absorption shift. More densely packed AuNPs were detected from the absorption spectra for higher AuNP content at which the ζ potential disappeared, while a split absorption band was also found, indicating that not all AuNPs can form a complex with AC at ζ = 0.

Novel polyamide nanofiltration membrane PEI-(β-CD@g-C3N5)/TMC based on microfiltration substrate for efficient separation of lithium and magnesium

With the development of industry, the scarcity of lithium resources is becoming increasingly prominent. Therefore, the development of high-performance nanofiltration (NF) membranes for lithium extraction from salt lakes has become crucial. Herein, β-Cyclodextrin (β-CD) and amino-rich graphitic carbon nitride (g-C3N5) sol were uniformly mixed to form β-CD@g-C3N5, which was then mixed with polyetherimide (PEI) monomer and subjected to interfacial polymerization (IP) reaction with trimesoyl chloride (TMC) on a 0.22 μm microfiltration (MF) membrane to prepare the PEI-(β-CD@g-C3N5)/TMC composite NF membrane. Through thin plate theory and gradient operation pressure filtration tests, it was found that the composite NF membrane prepared on the MF membrane substrate was not only defect-free but also exhibited superior compression resistance. In Li+/Mg2+ filtration tests, the PEI-(β-CD@g-C3N5)/TMC membrane showed superior NF performance, with a Li+/Mg2+ selectivity coefficient of 38.85 and a permeability of 8.91 L·m−2·h−1·bar−1. This was attributed to the effect of β-CD@g-C3N5, which could thin the separation layer, slightly enlarge and more uniformly distribute the pores, increase hydrophilicity, and enhance positive charge; meanwhile, the cavity structure provided by β-CD helped to effectively separate Li+/Mg2+. Furthermore, under conditions of mixed salt solutions with different Mg2+/Li+ mass ratios and 80 h of continuous filtration, the membrane exhibited excellent stability. This work introduces innovative membrane materials and design concepts to the field of lithium extraction via NF, potentially paving the way for the industrial application of NF technology.

Optimizing surface properties in pure titanium for dental implants: a crystallographic analysis of sandblasting and acid-etching techniques

Surface roughness is a critical factor affecting the performance of dental implants. One approach to influence this is through sandblasted, large grit, acid-etched (SLA) modification on pure titanium implant surfaces. In this study, SLA was performed on grade IV pure titanium. Sandblasting was conducted at distances of 2, 4, and 6 cm. Subsequently, the samples were etched with a mixed acid solution of HCl, H2SO4, and H2O for 0, 30, and 60 min. Surface roughness and X-ray diffraction (XRD) characterizations were conducted on the samples. The results revealed that surface roughness increased but was not too significant as the sandblasting distance decreased. Longer etching durations for sandblasted with acid-etched samples led to reduced surface roughness (Sa and Sz). It was found that a 60 min-etched sample resulted in optimal Sa, Sz, and Ssk values, i.e., 1.19 μm, 13.76 μm, and −0.60, respectively. The XRD texture was significantly influenced by sandblasting, with compressive residual stress increasing as the sandblasting distance decreased. Normal stress causes hill formations at shorter sandblasting distances. For etched samples, the residual stress decreased with longer etching durations. Normal stress-decreasing trend aligns with the initial reduction in hill and valley within the samples and subsequent hill enhancement at extended etching duration.

Exposing a dual-readout fibre calorimeter to electron beams, in preparation for HiDRa: High-resolution calorimeter for [formula omitted] colliders

Among the proposed accelerators for the post-LHC era are the Future Circular Collider (FCC) and the Circular Electron–Positron Collider (CEPC). Both projects would take advantage of the clean environment and low radiation damage of electron–positron collisions, providing the highest precision studies of electroweak and Higgs physics. The relatively high branching fraction of W, Z and Higgs bosons into hadronic jets makes the precise measurements of these objects an essential aspect on detector development for experiments at future collider facilities. One of the most promising calorimetry techniques for improved hadron energy reconstruction is the dual-readout method, which exploits signals from two different physics processes to correct for the fem of hadron showers, therefore boosting the standalone calorimeter performance. The usage of compact photosensors (e.g. Silicon PhotoMultipliers) for the readout enables a very fine segmentation, opening to particle-flow and advanced neural networks software reconstruction of events. In this contribution, the results of testing a small-scale dual-readout calorimeter prototype, characterised by a mixed PMT and SiPM readout solution, with an electron beam at the CERN SPS facility in the energy range [10, 120] GeV are presented. It follows the description of a larger prototype of the same type, currently under construction in the context of the INFN HiDRa project, that will be large enough to fully contain hadron showers. The design, construction technique and expected performance, as estimated through a Geant4 simulation parameterised on the previous prototype, are presented.