Linear polydichlorophosphazene and Ti3C2Tx MXene nanohybrids: Synthesis and application to epoxy resin to improve the fire safety and mechanical properties.

Enhancing the fire safety of epoxy resins (EPs) typically requires a significant amount of flame retardants, which often results in considerable degradation of their mechanical properties. To address this issue, a novel flame retardant known as PDCP@DPA@MXene was synthesized and integrated into EP to achieve notable improvements in flame retardancy, smoke suppression, and mechanical strength. By incorporating 1.5 wt% PDCP@DPA@MXene, the impact strength, tensile strength, and elongation at break of the resulting PDM-1.5 %/EP composite reached 12.1 kJ/m2, 57.4 MPa, and 13.0, respectively, reflecting enhancements of 63.5 %, 18.4 %, and 17.1 % compared to the pure EP. The enhancement in tensile strength may be attributed to the high rigidity of Ti3C2Tx MXene, which reinforces the EP matrix. Additionally, the intertwined structure of PDCP@DPA@MXene chains effectively mitigates material fracturing and absorbs impact forces, thus toughening the EP. The presence of phosphorus, nitrogen, and titanate in PDCP@DPA@MXene contributes to the formation of a more compact char layer. The PDM-1.5 %/EP sample achieved a V-0 rating in the vertical UL-94 test and exhibited a high limiting oxygen index of 32.0. Furthermore, the sample containing 2 wt% PDCP@DPA@MXene showed a significant reduction in peak heat release rate (p-HRR) and total heat release (THR), recording values of 689 kW/m2 and 71.9 MJ/m2, which are decreases of 45.1 % and 26.9 %, respectively, compared to pure EP. Additionally, the incorporation of PDCP@DPA@MXene led to a reduction in CO production. These flame-retarded EPs demonstrate strong potential for various applications due to their elevated glass transition temperature and robust thermal stability.

Construction of sustainable and highly efficient fire-protective nanocoatings based on polydopamine and phosphorylated cellulose for flexible polyurethane foam.

Layer-by-layer (LBL) self-assembly is an effective strategy for constructing fire-resistant coatings on flexible polyurethane foam (FPUF), while the efficiency of fire-resistant coatings remains limited. Therefore, this study proposes an in situ flame retardancy modification combined with LBL self-assembly technology to enhance the efficiency of flame retardant coatings for FPUF. Initially, polydopamine (PDA) and polyethyleneimine (PEI) were employed to modify the FPUF skeleton, thereby augmenting the adhesion on the surface of the skeleton network. Then, the self-assembly of MXene and phosphorylated cellulose nanofibers (PCNFs) via the LBL technique on the foam skeleton network formed a novel, sustainable, and efficient flame retardant system. The final fire-protective coatings comprising PDA/PEI and MXenes/PCNF effectively prevented the collapse of the foam structure and suppressed the melt dripping of the FPUF during combustion. The peak heat release rate, the peak CO production rate and peak CO2 production rate were reduced by 68.6 %, 61.1 %, and 68.4 % only by applying a 10-bilayer coating. In addition, the smoke release rate and total smoke production were reduced by 83.3 % and 57.7 %, respectively. This work offers a surface modification approach for constructing highly efficient flame retardant coatings for flammable polymeric materials.

Ti-Doped Tunnel-Type Na4Mn9O18 Nanoparticles as Novel Anode Materials for High-Performance Supercapacitors.

Nanomaterials with tunnel structures are extremely attractive to be used for electrode materials in electrochemical energy storage devices. Tunnel-structured Ti-doped Na4Mn9O18 nanoparticles (TNMO-NPs) were synthesized by a facile and high-production method of the solid-state reaction with a high-energy ball-milling process. As electrode materials in the supercapacitor cell, the as-synthesized TNMO-NPs exhibit a high specific capacity of 284.93 mA h g-1 (0.57 mA h cm-2/1025.75 F g-1). A superior rate capability with a decay of 36% is achieved by increasing the scan rates from 2 to 25 mV s-1. To further explore the storage mechanism of Ti-doped Na4Mn9O18 materials, density functional theory (DFT) calculations were used to calculate the activation energy for the ion immigration in the electrode, and the results show that the minimum ion diffusion barrier energy is 0.272 eV, indicating that the sodium ions could insert into the system easily. Through the scan-rate-dependent cyclic voltammetry analysis, the capacity value indicates a mixed charge storage of capacitive behavior and Na+ intercalation progress. A maximum energy density of 77.81 W h kg-1 at a power density of 125 W kg-1 is achieved, and a high energy density of 54.79 W h kg-1 is maintained even at an ultrahigh power density of 3750 W kg-1. The TNMO-NP supercapacitors show excellent flexibility at various bent (0-180°) states. The capacitive performance of the TNMO-NPs makes them promising cathode materials for flexible supercapacitors with high specific capacities and high energy densities.