Excellent Dispersion Research Articles

The Synergistic Effect of Graphene Oxide in Epoxy Resin on Photocured Coating Films with Anticorrosion and Antibacterial Properties.

In this work, graphene oxide (GO) and epoxy-functionalized graphene oxide (GOSi) are chosen as additives and incorporated into epoxy resin (EP) for nanocomposite photo-coating films (GO/EP and GOSi/EP series). Compared to GO/EP, the GOSi/EP nanocomposite demonstrates strong binding and excellent dispersibility, highlighting covalent bonding between GOSi and the epoxy coating. Furthermore, GOSi/EP-based films demonstrated superior thermal stability and adhesion performance on galvanized steel plates. The corrosion performance of the coated galvanized steel is investigated using electrochemical impedance spectroscopy (EIS) and polarization curve analysis (Tafel). The effectiveness of corrosion protection is evaluated based on a combination of photoreactivity, crosslinking density, dispersity, and adhesion properties. Out of all the treated films, the film based on 0.1GOSi/EP exhibited the highest percentage of inhibition (98.89%) and demonstrated superior long-term anticorrosion stability. In addition, the 0.1GOSi/EP based formulation showed remarkable antibacterial activity against S. aureus, resulting in a 92% reduction. This work demonstrates the development of a facile, environmentally friendly functionalized graphene oxide/epoxy photocured film with superior dual functionalities in both anticorrosion and antibacterial properties. These advancements hold promising potential for impactful practical applications.

Facile modification method for the controlled synthesis of dumbbell-like gold nanoparticles (AuNDBs) for application in detecting glucose using the SERS method

Dumbbell-like nanoparticles, previously known for their excellent light absorption and dispersion, have diverse applications, especially in SERS. Herein, we have explored a fast and novel controlled synthesis approach to achieve a high formation of AuNDBs. Precise control of precursor amounts and seed addition order halted seed growth at the AuNDB formation stage, preventing further elongation into rod-like structures. The AuNDBs were functionalized with 4-mercaptobenzoic acid (4-MBA) to create SERS nanosubstrates and deposited on the glass slide through 3-mercaptopropyl (dimethoxy)methylsilane by the spin-coating technique. The detection of d-glucose was achieved by measuring the signal decrease of the 4-MBA Raman probe molecules on the nanosubstrates at different trace concentrations of the analyte. These novel SERS substrates have the potential to provide an enhancement factor (EF) of 2.41 × 107 and a limit of detection (LOD) as low as 1.17 nmol/L. The electromagnetic field distribution of AuNDBs with many arrangements surrounded by air and d-glucose solutions was also determined by using the finite-difference time-domain technique (FDTD). The FDTD results confirmed that d-glucose on the SERS substrates caused the local electromagnetic field to degrade, resulting in the degree of the Raman signal. Our findings suggest that dumbbell-shaped SERS substrates can effectively detect very low levels of glucose, making them ideal for designing novel anisotropic nanoparticle-functionalized surfaces with ease.

Melt compounding of spray-dried cellulose nanofibrils/polypropylene and their application in 3D printing

Micro- and nano-scale cellulosic fillers exhibit excellent dispersion and distribution within a thermoplastic matrix during the process of melt compounding or injection molding. In this study, spray-dried cellulose nanofiber (SDCNF) powders were manufactured using a pilot-scale rotating disk atomizer spray dryer. Bleached Kraft pulp (BKP), unbleached Kraft pulp (UKP), and old corrugated cardboard pulp (OCC) fibrillated at a fines level of 90% were used as feedstock materials for spray-drying. BKP-, UKP-, and OCC- SDCNFs were compounded with polypropylene using a twin screw co-rotating extruder. Maleic anhydride grafted polypropylene (MAPP) was used as a coupling agent in the composite formulations. The tensile, flexural, and impact properties of SDCNF-filled PP composites increased at 10 wt% SDCNF loading. The presence of SDCNFs in the PP matrix resulted in faster crystallization and a 12% reduction in the degree of crystallinity of the neat PP. The coefficient of thermal expansion (CTE) of neat PP was reduced by up to 31% attributable to the presence of the SDCNFs. Application of the SDCNF-reinforced PP composites in 3D printing reduced the shrinkage rate of the printed neat PP by 39%, and the printability of the PP was significantly improved with the addition of the SDCNFs.

Electro-thermal actuation in recycled aggregate concrete with rapid self-reinforcement via smart cement-based composites

With the growing call for low-carbon and environmentally friendly materials, recycled aggregate concrete (RAC) holds great promise for sustainable development. Nevertheless, significant challenges exist with respect to the material’s poor flexural carrying capacity. Development of an effective method for improving the flexural carrying capacity of RAC under a specific deflection deformation is important for enhancing the range of its structural applications. In this study, an intelligent structural optimisation strategy for compounding RAC with carbon-fibre (CF) reinforced cement-based composites (CFRCs) to realize rapid self-reinforcement via electro-thermal actuation is proposed. As a smart component, CFRC was first researched to investigate its electrical, mechanical, and microscopic properties. The optimal properties were obtained in specimens incorporating 0.5 vol%, CFRC0.5. CFRC0.5 exhibits an electrical resistivity of approximately 0.39 Ω∙m, accompanied by 65.3 % and 33 % increases in flexural and compressive strengths, respectively, when compared to the control mixture without CF. Furthermore, CFRC0.5 can maintain outstanding stability after multiple electro-thermal cycles. Analysis via microscopic characterisation revealed that a satisfactory conductive network can be formed at 0.5 vol% CF. Furthermore, CFs with excellent dispersity are particularly advantageous in improving the mechanical biting force within the cement matrix and restraining the further formation and expansion of microcracks. Thus CFRC0.5 was designed and fabricated as a pre-stress controller to realise rapid structural self-reinforcement, resulting in a 38.6 % improvement in the flexural carrying capacity of the RAC under specific midspan deflection conditions. Additionally, a response behaviour model for midspan deflection with temperature differential was established, showing an excellent correlation between the experimental results and theoretical simulation. This findings from this study highlight the significance of leveraging intelligent techniques to realise rapid self-reinforcement capabilities in concrete structures, facilitating their potential application in smart and adaptive structures.

Performance repair of building materials using alumina and silica composite nanomaterials with electrodynamic properties

Abstract In recent years, the service life of building materials has become the focus of attention. Among them, the service life of concrete and steel bars is particularly affected by the corrosion of external ions (such as Cl−) in the environment. To solve this problem, a new type of composite nanocolloid was prepared through a controllable preparation method. The composite nanocolloid is prepared from aluminum chloride sol and silica sol as raw materials. The prepared colloidal particles have a particle size distribution between 10.5 and 17.5 nm, exhibiting excellent stability and dispersibility. In order to verify the improvement effect of the composite nanocolloid on the properties of building materials, the influence of it on the porosity of concrete and the anti-corrosion performance of steel bars was experimentally studied. The results indicate that the moisture absorption and dehumidification speed of concrete treated with composite nano colloids is slower, and the pore size distribution is mainly concentrated in 100–1,000 nm, indicating that the colloids can effectively optimize the pore structure of concrete. In addition, the processed steel plate samples showed high AC impedance values and low corrosion current logarithmic values in electrochemical testing, indicating that composite nanocolloids have a significant protective effect on the corrosion of steel bars, which can effectively improve the performance of building materials and extend their service life.

Densely Branched Carbon Nanotubes for Boosting the Electrochemical Performance of Li-S Batteries.

To address the inherent limitations of conventional carbon nanotubes (CNTs), such as their tendency to agglomerate and scarcity of catalytic sites, the development of branched carbon nanotubes (BCNTs) with a unique hierarchical structure has emerged as a promising solution. Herein, gram scale quantities of densely branched and structurally consistent Ni-Fe decorated branched CNTs (Ni-Fe@BCNT) have been prepared. This uniform and densely branched architecture ensures excellent dispersibility and superior electrical conductivity. Additionally, each branched tip is equipped with Ni-Fe particles, thereby providing numerous catalytic sites which endow them with exceptional catalytic activity for the conversion of polysulfides. The polypropylene (PP) separator modified with Ni-Fe@BCNT interlayer is fabricated as a multifunctional barrier for Li-S batteries. The experimental results demonstrate that Ni-Fe@BCNT interlayer can effectively suppress the shuttle effect of polysulfides and enhance their redox kinetics. The outstanding catalytic ability of Ni-Fe@BCNT interlayer enables batteries with high specific capacities, outstanding rate performance, and remarkable cycling stability. This approach proposed in this work paves a new path for synthesizing BCNTs and shows great potential for scaling up the production of BCNTs to address more demanding applications.

Preparation of MnO2 modified winter melon-derived biochar for enhanced adsorption of U(VI) from aqueous solution

Abstract This work synthesized MnO2 modified winter melon-derived biochar (MnO2@WBC) using potassium permanganate oxidation/hydrothermal method for uranium(VI) removal. The factors influencing uranium(VI) adsorption by MnO2@WBC, including pH, adsorbent dosage, time, temperature, and initial U(VI) concentration were explored. The material’s performance was characterized, and the underlying mechanism of U(VI) removal was analyzed using various techniques. The characterization results indicated that the MnO2@WBC exhibited excellent dispersibility, suggesting that MnO2 effectively prevented WBC aggregation and enhanced the reactive surface area, and providing more active sites that can effectively promote the complexation and adsorption of U(VI). The process suggested a dominant role for chemical adsorption. The Freundlich isotherm model demonstrated a high degree of alignment with the observed adsorption behavior, indicating a predominantly multilayer adsorption process. Thermodynamic studies indicated that adsorption was a spontaneous endothermic process. The XPS analysis demonstrated that the adsorption process was primarily due to the formation of stable complexes with C–O, Mn–O–H and C=O. The results demonstrated that MnO2@WBC effectively removed U(VI), achieving a maximum adsorption capacity of 240.86 mg g−1 at a pH of 5.0. These findings provided a theoretical basis for the treatment of wastewater contaminated with U(VI).

Foam drainage agent with enhanced foam stability through modified Fe3O4 nanoparticles

A nanofoam drainage agent was developed to address the challenges of inadequate foam stability and foaming efficiency in the gas recovery process of foam drainage. The formulation of the primary foam drainage agent was obtained by screening and combining conventional anionic and amphoteric surfactants. Experimental results revealed a synergistic interaction between α-olefin sulfonate (AOS) and lauramidopropyl betaine (LAB-35). Specifically, when a mixture of 0.4 wt.% AOS and 0.1 wt.% LAB-35 was used, the surface tension of the primary foam drainage agent was measured to be 23.32 mN/m. Furthermore, modification of Fe3O4 nanoparticles with the silane coupling agent γ-(methacryloxy)propyl trimethoxysilane (KH-570) was performed to improve the dispersibility in aqueous solutions and enhance foam stability. The results of infrared spectroscopy, x-ray diffraction, thermogravimetric analysis, and contact angle measurements revealed the effective bonding of KH-570 to the surface of Fe3O4 nanoparticles. Additionally, the particle size distribution in the aqueous solution showed the excellent dispersion of the modified Fe3O4 nanoparticles. Through the incorporation of the modified Fe3O4 nanoparticles into the primary foam drainage agent, a nanofoam drainage agent with a half-life of 989 ± 6.5 s was developed. Microscopic observations of foam coarsening behavior revealed the mechanism behind foam stability. Performance testing of the foam drainage agent demonstrated the agent’s outstanding resistance against salinity, temperature, and oil and its remarkable liquid-carrying capacity.

Preparation and thermal properties of latent functional thermal fluid based on size-controllable phase change nanocapsules

Size-controllable 1-octadecanol@polystyrene phase change nanocapsules (NEPCMs) were prepared using the miniemulsion polymerization and dispersed in deionized water containing multi-walled carbon nanotubes to prepare a latent functional thermal fluid (LFTF). The results demonstrate that the NEPCMs exhibit a typical core-shell structure. The average particle size (55.28–143.8 nm) of the NEPCMs can be regulated by controlling the content of compound emulsifiers. The optimal phase change enthalpy has an excellent heat storage capacity of about 222.7 J/g, the encapsulation efficiency is up to 80.63 %, and the average particle size is about 88.3 nm. The heating/cooling cycles results show that NEPCMs have excellent cycle stability. LFTF containing 10 wt% NEPCMs was considered the optimal choice for its excellent photothermal conversion efficiency (up to 64.91 %), excellent dispersion stability (zeta potential 39.17 mV) and thermal storage capacity (peak specific heat capacity 5.72 J g−1 K−1). Under the influence of solar radiation, the temperature rise curve of LFTF exhibited a rapid initial warming rate followed by a plateau period of approximately 76 min upon reaching the melting point of the NEPCMs, whose photothermal conversion efficiency is roughly 2.18 times that of water. The experimental findings demonstrate the potential application of LFTF based on NEPCMs in the solar thermal industry.

Tribological Effects of Quaternary Ammonium-Functionalized Montmorillonite as Water-Based Additives.

In this study, a water-soluble quaternary ammonium salt (QAS)-functionalized montmorillonite (MMT) was fabricated using a mechanochemical method as a high-performance water lubrication additive. The intercalation of QAS into the MMT layer expands the layer spacing of MMT, but does not affect the hydrophilicity of MMT. The ultrathin layer QAS-functionalized montmorillonite (QAS-MMT) demonstrated excellent water-stable dispersion and can be used as a water-based lubrication additive. Only 0.1% addition can reduce the friction coefficient by more than 71.4% and the wear volume by about 58.8% when compared to water, demonstrating its excellent friction reduction and antiwear performance. The frictional mechanism indicates that the physical adsorption film, together with the chemical reaction film, endows the QAS-MMT additives with outstanding tribological performance, provides excellent lubrication for the contact of steel/steel pairs, and prevents the steel surface from being further worn.

Dispersion effect of nano-structure pyrolytic carbon on mechanical, electrical, and microstructural characteristics of cement mortar composite

ABSTRACT In material science, converting waste into nanomaterials by green technologies highlights the interest in producing sustainable carbon nanomaterial (SCN). This study first-ever utilized tyre-char as a Nano-Structure Pyrolytic Carbon (NSPC) to develop electrically conductive composites. Unlike other carbon nanomaterials, the efficiency of NSPC particle as an SCN in developing electrically conductive composites was investigated in terms of dispersion, mechanical, water absorption, electrical resistivity, and microstructure. The results of sedimentation and zeta potential (−19 mV) showed the excellent dispersion of NSPC particle in water with the combined effect of superplasticizer and ultrasonication. The compressive (40.37%) and flexural strength (10.76%) than that of plain cement mortar composite (CMC) is achieved with 2 wt.% and 1.5 wt.% of NSPC particle, respectively. The water absorption rate and volume of permeable voids were reduced, exhibiting less agglomerations. The percolation zone of AC and DC resistivity of NSPC composite ranges between 1 and 2 wt.%, and the established percolation threshold is at 2 wt.%. XRD analysis showed C-S-H formation consistently increased with curing age, and HR-SEM with EDAX analysis exhibits the dense microstructure and well-distributed NSPC particle at the nanoscale. These experimental outcomes significantly enhanced the reliability and provided a framework for tailoring NSPC particle as SCN for developing electrically conductive composite.

Dispersion Strategy improves the mechanical properties of 3D-Printed biopolymer nanocomposite

Homogenous dispersion of nanoparticles in polymer matrices is a technical challenge that if overcome can lead to improved mechanical properties of the resulting nanocomposites. In this work, we successfully refined commercially-available nanoscale, calcium deficient, and poorly crystalline hydroxyapatite (nHA) particles and composited them with acrylate and methacrylate functionalized soybean oil (mAESO) and triethylene glycol dimethacrylate (TEGDMA) producing inks for masked stereolithography (mSLA) -based 3D printing. First, we used shear mixing and ultrasonication on nHA/ethanol mixtures to break down agglomerates and then separated the finest nanoparticles from the remaining agglomerates using centrifugation. The refined nanoparticles (termed fine) were then mixed with the resins and UV-initiator to produce inks for 3D printing. Similarly, we prepared one ink using as-purchased nHA particles (termed raw) and another ink using leftover agglomerates after refinement (termed coarse). We compared the rheological properties of the nHA-resin inks. We used mSLA to fabricate nanocomposite specimens and tested them using flexural, and Mode-I fracture toughness testing following ASTM standards. The dispersion of nanoparticles in the polymer matrix was studied by analyzing backscattered mode scanning electron microscopy images. The nHA particle refinement improved the nanoparticle dispersion in the resin matrix while also increasing the viscosity and shear yield strength of the nanocomposite ink. The flexural fracture strength, flexural modulus, and Mode-I fracture toughness of refined nHA-based nanocomposites were increased by 11 %, 71 %, and 12 %, respectively compared to the raw nHA-based nanocomposites. However, the flexural fracture strain of refined nHA-based nanocomposites was lower by 40 % compared to the raw nHA-based nanocomposites. The nanocomposites became stiffer with the incorporation of refined nanoscale nHA. The separation of nanoscale nHA particles, excellent dispersion of these nanoparticles in polymer matrix, and improved flexural strength and modulus opens a new avenue towards the 3D printing of high-performance nHA-based nanocomposites.

Natural and polyanionic heparin polysaccharide functionalized upconversion nanoparticles for highly sensitive and selective ratiometric detection of pesticide

Pesticide contamination is a global concern, threatening human health and food safety. Herein, we developed heparin (HEP) functionalized upconversion nanoparticles (UCNPs)-based ratiometric nanosensor for the sensitive detection of 2,6-dichloro-4-nitroaniline (DCN) pesticide via inner filter effect. The strategy for HEP functionalization of UCNPs is based on adjusting the surface potentials of UCNPs with polyanionic HEP through the electrostatic interaction. UCNPs (NaYbF4:Gd/Y/Tm@NaYbF4@NaYF4) was designed with core-shell-shell structure and extra sensitizer layer for efficient and strong upconversion luminescence (UCL) in the range of UV to NIR. After incorporation of DCN, the upconverted UV emission of UCNPs-HEP ratiometric nanosensor was considerably quenched with the NIR UCL at 800 nm remaining unchanged as internal standard. The UCNPs-HEP ratiometric nanosensor can achieve outstandingly selective and sensitive detection of DCN at the wide linear range of 5–300 μM with a detection limit of 0.41 μM. The remarkable applicability of the UCNPs-HEP ratiometric nanosensor was verified in apple, cucumber and grapes samples. The developed UCNPs-HEP ratiometric nanosensor with excellent biocompatibility and water dispersion capability, is promising for convenient, selective and sensitive sensing of DCN towards food and aqueous samples.

Improved carbon fibers dispersion in geopolymer composites

Carbon fibers (CFs) reinforced alkali-activated (AA) ground granulated blast furnace slag (GGBFS) geopolymer composites have excellent mechanical and thermoelectrical properties, as well as low energy consumption and low CO2 emissions during their production. However, the dispersion of CFs in the geopolymer matrix is always a technical issue in the preparation of the green composite material. Therefore, this study comparatively investigated various dispersion methods, including, mixing sequence (pre-mixing and after-mixing methods), dispersing agent (nano silicon dioxide [nSiO2]), and ultrasonic treatment time (0, 15, 30, and 45 min), as well as CFs content (0.5, 1.0, and 1.5 wt% of GGBFS). The distribution of CFs was then qualitatively and quantitatively evaluated by a series of tests, such as flowability, electrical resistivity, flexural strength, scanning electron microscope (SEM) analysis, and X-ray computed tomography (CT). The experimental results showed that the proposed pre-mixing method provided excellent dispersion characteristics for CFs compared with the after-mixing method. The introduction of nSiO2 can enhance the dispersion of CFs and the mechanical and electrical properties of AA GGBFS geopolymer composites. At a carbon fiber content of 1.5 %, the pre-mixing method and the addition of nSiO2 dispersant reduced the resistivity of the 28-day geopolymer composites by 17.0 % and 38 %, respectively, compared with the after-mixing method. It is feasible to use X-ray CT scanning with the gray-scale frequency map to analyze the dispersion effect of CFs in AA GGBFS geopolymer composites. However, the results were not intuitive when less agglomeration of CFs occurred for the low content of CFs. The scanning method is more applicable to the sample with over 1.0 wt% CFs. The average pixel areas of uniformly dispersed CF bundles in the 2D images of the pre-mixing method and the addition of nSiO2 dispersant specimens were 3.32 % and 6.55 % higher than those of the after-mixing method, respectively. The 2D and 3D scanning results from the dispersion characteristics of CFs were consistent. 2D scanning could provide a time-consuming option for the measurement of CFs dispersion characteristics.

Development and characterization of tobacco suspension cell chassis NBS-1

Plant synthetic biology has significant theoretical advantages in exploration and production of plant natural products. However, its contribution to the field of biosynthesis is currently limited due to the lack of efficient chassis systems and related enabling technologies. Synthetic biologists often avoid tobacco as a chassis system because of its long operation cycle, difficulties in genetic and metabolic modification, complex metabolism and purification background, nicotine toxicity, and challenges in accurately controlling for agricultural production. Nevertheless, the tobacco suspension cell chassis system offers a viable solution to these challenges. The objective of this research was to develop a tobacco suspension cell chassis with high scientific and industrial potential. This chassis should exhibit rapid growth, high biomass, excellent dispersion, high transformation efficiency, and minimal nicotine content. Nicotiana benthamiana, which has high applicability in molecular technology, was used to induce suspension cells. The induced suspension cells, named NBS-1, exhibited rapid growth, excellent dispersion, and high biomass, reaching a maximum biomass of 476.39 g/L (fresh weight), which was significantly higher than that of BY-2. The transformation efficiency of the widely utilized pEAQ-HT transient expression system in NBS-1 reached 81%, which was substantially elevated compared to BY-2. The metabolic characteristics and bias of BY-2 and NBS-1 were analyzed using transcriptome data. It was found that the gene expression of pathways related to biosynthesis of flavonoids and their derivatives in NBS-1 was significantly higher, while the pathways related to alkaloid biosynthesis were significantly lower compared to BY-2. These findings were further validated by the total content of flavonoid and alkaloid. In summary, our research demonstrates NBS-1 possesses minimal nicotine content and provides valuable guidance for selecting appropriate chassis for specific products. In conclusion, this study developed NBS-1, a tobacco suspension cell chassis with excellent growth and transformation, high flavonoid content and minimal nicotine content, which has important guiding significance for the development of tobacco suspension cell chassis.

Ultra‐deep and fast oxidative desulfurization by IL‐POM immobilized on bar‐shaped green fiber toward the high efficiency

The Keggin‐type P‐Mo‐W polyoxometalate‐based ionic liquids ([VimAm]Br‐POM, POM is PMo6W6O40) were facilely supported on the green fiber (CA) to obtain a kind of bar‐shaped catalyst. The [VimAm]Br‐POM@CA showed an outstanding oxidative desulfurization performance for model oil and real oils with H2O2 as oxidant, mainly due to the dual role of the [VimAm]Br‐POM with the high activity and its excellent dispersion on CA. The dibenzothiophene (DBT) in model oil could be almost completely removed with [VimAm]Br‐POM@CA‐2 in 60 min at 60 °C without adding other extractants, in which [VimAm]Br acts as this role. Meanwhile, the influences of reaction temperature, molar ratio of H2O2/S, catalyst dosage, and different sulfur‐containing compounds were also investigated. Interestingly, the pretty low activation energy (0.1875 kJ/mol) has been achieved, and no significant loss of activity even after being reused for 5 cycles. The combination of IL‐POM and CA is an efficient strategy to obtain a newly kind desulfurization catalyst, with remarkable results on catalytic efficiency and reuse ability at the same time.

Transparent and High-Refractive-Index Titanium Dioxide/Thermoplastic Polyurethane Nanocomposites.

Transparent nanocomposite films made of surface-modified titanium dioxide nanoparticles and thermoplastic polyurethane are prepared via film casting approach showing enhanced refractive indexes and mechanical properties. Two different sets of composites were prepared up to 37.5 wt % of inorganic nanoparticles with a diameter <15 nm, one set using particles capped only with oleic acid and a second one with a bimodal system layer made of oleic acid and mPEO-5000 as coating agents. All of the composites show significantly enhanced refractive index and mechanical properties than the neat polymeric matrix. The transparency of nanocomposite films shows the excellent dispersion of the inorganic nanoparticles in the polymeric matrix avoiding aggregation and precipitation phenomena. Our study provides a facile and feasible route to produce transparent nanocomposite films with tunable mechanical properties and high refractive indices for various applications.

The Synthesis of Copper Nanoparticles for Printed Electronic Materials Using Liquid Phase Reduction Method.

This text discusses the synthesis of copper nanoparticles via a liquid phase reduction method, using ascorbic acid as a reducing agent and CuSO4·5H2O as the copper source. The synthesized copper nanoparticles are small in size, uniformly distributed, are mostly between 100-200 nm with clear boundaries between particles, and exhibit excellent dispersibility, making them suitable for metal conductive inks. 1. The copper nanoparticles are analyzed for good antioxidation properties, because their surface is coated with PVP and ascorbic acid. This organic layer somewhat isolates the particle surface from contact with air, preventing oxidation, and accounts for about 9% of the total weight. 2. When the prepared copper nanoparticles are spread on a polyimide substrate and sintered at 250 °C for 120 min, the resistivity can be as low as 23.5 μΩ·cm, and at 350 °C for 30 min, the resistivity is only three times that of bulk copper. 3. The prepared conductive ink, printed on a polyimide substrate using a direct writing tool, shows good flexibility before and after sintering. After sintering at 300 °C for 30 min and connecting the pattern to a circuit with a diode lamp, the diode lamp is successfully lit. 4. This method produces copper nanoparticles with small size, good dispersion, and antioxidation capabilities, and the conductive ink prepared from them demonstrates good conductivity after sintering.

Penetrative Ionic Organic Molecular Cage Nanozyme for the Targeted Treatment of Keratomycosis.

Keratomycosis, caused by pathogenic fungi, is an intractable blinding eye disease. Corneal penetration is an essential requirement for conventional antifungal medications to address keratomycosis. Due to the distinctive anatomical and physiological structure of the cornea, the therapeutic efficacy is hampered by the inadequate penetration capacity. Despite the emergence of diverse antifungal drug delivery systems and advanced antifungal nanomaterials, it has remained challenging to achieve corneal penetration over the past decade. This study fabricates a penetrative ionic organic molecular cage-based nanozyme (OMCzyme) for treating keratomycosis. The synthesis of OMCzyme involved two steps. Initially, the ionic OMC is synthesized by a [2+3] cycloimination reaction of triformylphloroglucinol and 2,3-diaminopropionic acid. Subsequently, OMCzyme is fabricated by coordination of Fe2⁺ with carboxyl anions and phenolic hydroxyls in the organic cage, and further deposition of silver nanoparticles on the surface of OMC-Fe complex. The as-prepared OMCzyme demonstrates excellent water dispersion, peroxidase-like activity, in vitro and in vivo biocompatibility, and corneal penetration. Notably, the nanozyme displays targeted antifungal activity, effectively combating Fusarium solani with negligible cytotoxicity toward human corneal epithelial cells. The hybrid mimic is further demonstrated to be effective in treating keratomycosis in mice, indicating the potential of OMCzyme for curing fungal infectious diseases.

Magnetic surface-imprinted polymer microspheres coupled with HPLC-MS/MS for sensitive detection of amphetamine-type drugs in water

Magnetic surface imprinted polymer microspheres (Fe3O4@MIPs) were successfully synthesized via Pickering emulsion polymerization, utilizing N-Methylphenethylamine as a surrogate template for amphetamine-type drugs. Fe3O4@MIPs not only possessed excellent dispersibility and enough magnetic properties in aqueous solutions, but also displayed good selectivity towards six amphetamines, with an imprinting factor ranging from 1.8 to 2.6. The adsorption kinetics closely aligned with the pseudo-second-order model, and the adsorption efficiency exceeds 80 % for each amphetamine at equilibrium. Fe3O4@MIPs were then employed as the efficient adsorbents for the extraction of amphetamine drugs. Extraction parameters, including sample pH, the mass of adsorbent, and the type and volume of eluting solvent, were carefully optimized. In combination with the high performance liquid chromatography tandem triple quadrupole mass spectrometry (HPLC-MS/MS), a selective magnetic solid-phase extraction (MISPE) method utilizing Fe3O4@MIPs was developed for the detection of six amphetamines in water samples. The limits of detection and limits of quantitation were determined to be 5.2∼23 ng L−1 and 17∼77 ng L−1, respectively. Recoveries for the six target drugs from lake water and sewage samples fell within the range of 87.2∼110 %. Additionally, the MISPE-HPLC-MS/MS method exhibited excellent repeatability, with a precision below 8.5 % at two spiking levels. The prepared Fe3O4@MIPs possessed the advantages of high selectivity, straightforward preparation, facile separation and good reusability, and was highly suitable for the efficient extraction of amphetamine-type substances in complex environmental water.