Publications by authors named "Meishuai Zou"

Modified basalt microfiber-reinforced polyurethane elastomer composites were prepared by a semi-prepolymer method with two different silane coupling agents (KH550 and KH560) in this study. Infrared spectroscopy was used to quantify the degree of microphase separation and analyze the formation of hydrogen bonding in polyurethane. The interfacial surface and the morphology of fibers and composites from tensile fracture were examined by a scanning electron microscope.

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Elastomers are of great significance in developing smart materials for information encryption, and their unique self-healing and highly flexible properties provide innovative solutions to enhance security and anti-counterfeiting effectiveness. However, challenges remain in the multifunctional combination of mechanical properties, self-healing, degradability, and luminescence of these materials. Herein, a chemodynamic covalent adaptable network (CCAN)-induced robust, self-healing, and degradable fluorescent elastomer is proposed.

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Polymer materials are highly vulnerable to fire disaster. However, current research focuses on flame retardancy rather than protection. In this work, two natural extracts of phytic acid (PA) and tannic acid (TA), were successfully compounded via dual-nucleophilic esterification, which facilitated the formation supramolecular hydrogel (T-P-PAA).

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Polyurethane incorporated with nanofillers such as carbon nanotubes, basalt fibers, and clay nanoparticles has presented remarkable potential for improving the performance of the polymeric composites. In this study, the halloysite nanofiller-reinforced polyurethane elastomer composites were prepared via the semi-prepolymer method. The impact of different halloysites (halloysite nanotubes and halloysite nanoplates) in polyurethane composites was investigated.

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Vanadium tetrasulfide (VS) is one of the most promising cathodic materials for rechargeable magnesium battery systems (RMBSs). Elemental substitution to expand layers, creation of sulfur vacancies, and reduction of particle sizes of VS are undoubtedly effective strategies to enhance cathodic performances. Experimental and DFT analysis revealed that valence states of vanadium and cobalt have been elevated from V to V and Co to Co in VS and that the Co-S bond length shortened due to cobalt substitution, which resulted in enhanced overall internal polarization in the layered atomic structure of VS by increasing cobalt concentrations.

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Article Synopsis
  • Surface modification is commonly used to enhance the combustion properties and reduce agglomeration in aluminum-based fuels, but traditional methods result in uneven coatings that reduce performance.
  • A new technique using monolayer nano-vesicular self-assembly with a specially designed triblock copolymer called G-F-G leads to a uniform, thin coating (≈15 nm) on aluminum powder.
  • This innovative approach results in aluminum fuels with improved ignition, combustion, anti-agglomeration, and waterproof properties, which could influence the development of advanced energetic materials and other applications involving surface nanostructures.
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Constructing multiheteroatom coordination structure in carbonaceous substrates demonstrates an effective method to accelerate the oxygen reduction reaction (ORR) of supported single-atom catalyst. Herein, the novel etching route assisted by potassium thiocyanate (KCNS) is developed to convert metal-organic framework to 2D defect-rich porous N,S-co-doped carbon nanosheets for anchoring atomically dispersed iron sites as the high-performance ORR catalysts (Fe-SACs). The well-designed KCNS-assisted etching route can generate spatial confinement template to direct the carbon nanosheet formation, etching condition to form defect-rich structure, and additional sulfur atoms to coordinate iron species.

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  • Polyurethane microcellular elastomers (PUME) are effective for impact protection and energy absorption, and their behaviors depend on strain rate and past deformation.
  • The study investigated PUME with different densities (800 kg/m³, 600 kg/m³, 400 kg/m³) under varying strain rates and found that the 600 kg/m³ density exhibited the best compressive performance.
  • A new visco-hyperelasticity-air model was developed to describe PUME's deformation under high strain rates, and its parameters were verified using experimental data, enhancing simulation and application potential for energy absorption in protective designs.
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Article Synopsis
  • Flame retardants (FRs) can weaken the mechanical properties of polymers, prompting a study on FR/microcellular polyurethane elastomer (MPUE) composites using different liquid FRs and expandable graphite (EG).
  • The combination of expandable graphite and dimethyl methylphosphonate (EG/DMMP) significantly improved flame resistance (LOI up to ~36.1% and V-0 ratings) but decreased tensile strength by 17.5%, while EG alone maintained strength without a dripping hazard.
  • A balance of flame retardancy and mechanical properties was achievable with EG, and the proposed synthesis method is effective, low-cost, and versatile, enhancing potential applications for MPUEs.
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Aluminum powder plays important role in the field of energetic materials. However, it is often vulnerable to oxygen and water due to the high reactivity of aluminum, and it is challenging to build up uniform and passivated coating via existing means. In this work, (Heptadecafluoro-1,1,2,2-tetradecyl) trimethoxysilane (FAS-17) and glycidyl azide polymer (GAP) were used to coat the surface of high water-reactive aluminum powder (w-Al) to form inactivated w-Al@FAS-17@GAP energetic materials, via the synergy of chemical bonding and physical attraction.

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The curing kinetics of MDI-based polyurethane elastomers were studied by non-isothermal differential scanning calorimetry (DSC). The kinetic parameters of the reaction system were calculated by the Kissinger method. The changing activation energy was observed by the Flynn−Wall−Ozawa method and the Friedman method.

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The main problem for the application of hydrogen generated via hydrolysis of metal alloys is the low hydrogen generation rate (HGR). In this paper, active Al alloys were prepared using a new coupled method-melting-mechanical crushing-mechanical ball milling method to enhance the HGR at room temperature. This method contains three steps, including the melting of Al, Ga, In, and Sn ingots with low melting alloy blocks and casting into plates, then crushing alloy plate into powders and ball milling with chloride salts such as NiCl and CoCl were added during the ball milling process.

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The non-isothermal crystallization behaviors of poly (ethylene glycol) (PEG) and poly (ethylene glycol)-b-poly(ε-caprolactone) (PEG-PCL) were investigated through a commercially available chip-calorimeter Flash DSC2+. The non-isothermal crystallization data under different cooling rates were analyzed by the Ozawa model, modified Avrami model, and Mo model. The results of the non-isothermal crystallization showed that the PCL block crystallized first, followed by the crystallization of the PEG block when the cooling rate was 50-200 K/s.

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The non-isothermal crystallization kinetics of double-crystallizable poly(ethylene glycol)-poly(l-lactide) diblock copolymer (PEG-PLLA) and poly(ethylene glycol) homopolymer (PEG) were studied using the fast cooling rate provided by a Fast-Scan Chip-Calorimeter (FSC). The experimental data were analyzed by the Ozawa method and the Kissinger equation. Additionally, the total crystallization rate was represented by crystallization half time .

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In this paper, the dynamics of multi-dendrite concurrent growth and coarsening of an Al-15 .% Cu alloy was studied using a highly computationally efficient 3D phase field model and real-time synchrotron X-ray micro-tomography. High fidelity multi-dendrite simulations were achieved and the results were compared directly with the time-evolved tomography datasets to quantify the relative importance of multi-dendritic growth and coarsening.

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This study aimed to prepare a new lightweight ultra-high-voltage insulator core filler composite, which can solve the problem of bulkiness. In this study, rigid polyurethane foam pellets with different densities are used as lightweight fillers and polyurethane resins to compound lightweight composite materials. On accounting for working conditions, the density, insulation, heat resistance, water absorption and mechanical properties are tested.

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Epoxy resin is one of the commonly used matrixes of syntactic foams as a buoyancy material, the curing agents of which affect some of the properties for syntactic foams. Therefore, the curing reactions of ,,','-tetraepoxypropyl-4,4'-diaminodiphenylmethane (AG-80) epoxy resin between 4,4-diaminodiphenyl methane (DDM) and the mixture of -xylylenediamine and DDM (DDM--XDA) systems are studied. The DDM mixed with -XDA enhances curing reactions with the AG-80 epoxy resin, and the mechanisms of the two curing systems are different through nonisothermal kinetics.

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In order to synthesize a new kind of buoyancy material with high-strength, low-density and low-water-absorption and to study the curing reaction of tetraglycidylamine epoxy resin with an aromatic amine curing agent, the non-isothermal differential scanning calorimeter (DSC) method is used to calculate the curing kinetics parameters of N,N,N',N'-tetraepoxypropyl-4,4'-diaminodiphenylmethane epoxy resin (AG-80) and the m-xylylenediamine (m-XDA) curing process. Further, buoyancy materials with different volume fractions of hollow glass microsphere (HGM) compounded with a AG-80 epoxy resin matrix were prepared and characterized. The curing kinetics calculation results show that, for the curing reaction of the AG-80/m-XDA system, the apparent activation energy increases with the conversion rates increasing and the reaction model is the Jander equation (three-dimensional diffusion, 3D, n = 1/2).

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To systematically explore the effects of the synthesis conditions on the porosity of hyper-cross-linked polymers (HCPs), a series of 9-phenylcarbazole (9-PCz) HCPs (-) has been made by changing the molar ratio of cross-linker to monomer, the reaction temperature , the used amount of catalyst and the concentration of reactants. Fourier transform infrared spectroscopy was utilized to characterize the structure of the obtained polymers. The TG analysis of the HCPs showed good thermal stability.

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The emergence of drug-resistant bacteria is becoming the focus of global public health. Early-stage pathogen bioimaging will offer a unique perspective to obtain infection information in patients. A photoacoustic (PA) contrast agent based on functional peptide modified gold nanoparticles (AuNPs@P1) is developed.

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Buoyancy material is a type of low-density and high-strength composite material which can provide sufficient buoyancy with deep submersibles. A new buoyancy material with N,N,N',N'-tetraepoxypropyl-4,4'-diaminodiphenylmethane epoxy resin (AG-80) and m-xylylenediamine (m-XDA) curing agent as matrix and hollow glass microsphere (HGM) as the filler is prepared. The temperature and time of the curing process were determined by the calculations of thermal analysis kinetics (TAK) through differential scanning calorimetry (DSC) analysis.

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In this study, ferric perfluorooctanoate [Fe(PFO)] was used in the aluminized HTPB propellant to reduce Al agglomeration during solid propellant combustion, and the agglomeration reduction mechanism was experimentally demonstrated the burning rate measurement, heat of explosion and Al agglomeration analysis. The behavior of the burning particles on the burning surface as well as the morphology and composition of the quenched burning particles were characterized by microscopic high-speed photography and X-ray photoelectron spectroscopy, respectively; the thermal decomposition properties and gaseous decomposition products of Fe(PFO) were investigated by thermal gravimetry-differential scanning calorimetry joint analysis (TG-DSC), Fourier transform infrared spectroscopy (FTIR) and mass spectrometry (MS). The results show that Fe(PFO) can significantly increase the burning rate of the aluminized HTPB propellant and reduce Al agglomeration.

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