Search Results (190)

Silica fume-based geopolymer composite coatings, an approach to using metallurgical solid waste, exert flame retardancy with ecological, halogen-free, and environmentally friendly advantages, but their fire resistance needs to be improved further. Herein, a silica fume-based geopolymer composite flame-retardant coating was designed by doping boric acid (BA), zinc phytate (ZnPA), and melamine (MEL). The results of a cone calorimeter demonstrated that appropriate ZnPA and BA significantly enhanced its flame retardancy, evidenced by the peak heat release rate (p-HRR) decreasing from 268.78 to 118.72 kW·m⁻², the fire performance index (FPI) increasing from 0.59 to 2.83 s·m²·kW⁻¹, and the flame retardancy index increasing from 1.00 to 8.48, respectively. Meanwhile, the in situ-formed boron phosphate (BPO₄) facilitated the residual resilience of the fire-barrier layer. Furthermore, the pyrolysis kinetics indicated that the three-level chemical reactions governed the pyrolysis of the coatings. BPO₄ made the pyrolysis E_α climb from 94.28 (P5) to 127.08 (B3) kJ·mol⁻¹ with temperatures of 731–940 °C, corresponding to improved thermal stability. Consequently, this study explored the synergistic flame-retardant mechanism of silica fume-based geopolymer coatings doped with ZnPA, BA, and MEL, providing an efficient strategy for the high-value-added recycling utilization of silica fume. Full article

The inherent flammability and hydrophilicity of nylon/cotton (NC) blend fabrics limit their practical applications. Traditional hydrophobic treatments often involve fluorinated compounds or nanomaterials, which raise environmental concerns and exhibit poor durability. To address these issues, this study developed a sustainable multifunctional finishing strategy. Initially, the nylon/cotton blended fabric was pretreated with 3-glycidyloxypropyltrimethoxy silane (GPTMS). An intumescent flame retardant coating based on bio-derived phytic acid (PA) and polyethyleneimine (PEI) was constructed on NC fabrics via a layer-by-layer (LBL) self-assembly process. Subsequently, polydimethylsiloxane (PDMS) was grafted to reduce surface energy, imparting synergistic flame retardancy and superhydrophobicity. The treated fabric (C-3) showed excellent flame retardant and self-extinguishing behavior, with no afterflame or afterglow during vertical burning and a char length of only 35 mm. Thermogravimetric analysis revealed a residual char rate of 43.9%, far exceeding that of untreated fabric (8.6%). After PDMS modification, the fabric reached a water contact angle of 157.8°, indicating superior superhydrophobic and self-cleaning properties. Durability tests showed that the fabric maintained its flame retardancy (no afterflame or afterglow) and superhydrophobicity (WCA > 150°) after 360 cm of abrasion and five laundering cycles. This fluorine-free, nanoparticle-free, and environmentally friendly approach offers a promising route for developing multifunctional NC fabrics for applications in firefighting clothing and self-cleaning textiles. Full article

Incorporating a 9,10-dihydro-9-oxa-10-phosphaphenanthrene-10-oxide-based derivative (1,4-bis(diphenoxyphosphoryl)piperazine, DIDOPO) in combination with modified calcium sulfate whiskers (MCSWs) improved the flame retardancy, thermal stability, and rheological properties of a polyethylene oxide (PEO) composite. The synergistic flame-retardant effect of DIDOPO and MCSW on the PEO system was investigated. After introducing 5 wt.% MCSW and 10 wt.% DIDOPO into PEO, the UL-94 rating of the composite reached V-0, and the limiting oxygen index was increased to 26.5%. Additionally, the peak and average heat release rates and total heat release of the PEO/10% DIDOPO/5% MCSW composite decreased by 38.9%, 22%, and 20.07%, respectively. The results of a thermogravimetric analysis (TGA) revealed that PEO/10% DIDOPO/5% MCSW displayed an improved initial thermal stability and rate of char formation compared to those of the PEO matrix. The results of TGA/Fourier transform infrared analysis indicated that the composites exhibited phosphorus-containing groups during thermal degradation, based on the characteristic absorption peaks, and increased amounts of gas-phase volatiles. The morphologies and structures of the residues indicated that the PEO/10% DIDOPO/5% MCSW blend was less stable than PEO during combustion. The MCSW mixture formed a denser, more continuous carbon layer on the composite surface during combustion. The rheological behavior indicated that the high complex viscosity and moduli of PEO/10% DIDOPO/5% MCSW promoted the cross-linking network structure of the condensed phase during combustion. MCSW exhibited an excellent flame retardancy and improved thermal stability, which are potentially promising for use in fire safety applications. Full article

This study systematically examines the effect of the morphology of cerium oxide (CeO₂) on the flame retardancy, thermal stability, and mechanical properties of polypropylene composites with intumescent flame retardant (PP/IFR). Layer-CeO₂ (L-CeO₂) outperforms Particulate-CeO₂ (P-CeO₂) in enhancing the flame retardancy of PP/IFR composites, showing higher limiting oxygen index (LOI) and greater reductions in the total heat release rate (THR) and total smoke production (TSR). The substitution of 1% IFR with 1% L-CeO₂ significantly increased the LOI from 29.4% to 32.6%, while reducing the THR and TSR by 38.9% and 74.3%, respectively. L-CeO₂ incorporation improves thermal stability, increasing the residual char yield to 8.53% at 800 °C under air (vs. 3.87% for PP/IFR). Additionally, L-CeO₂ improved the mechanical properties of the composites, increasing tensile strength and rigidity. The synergistic flame-retardant mechanism is hypothesized to involve CeO₂ catalyzing the formation of a P-O-C crosslinked network in the carbon layer, leading to a denser carbon structure and improved flame-retardant performance in the PP/IFR composites. These findings demonstrate the efficacy of L-CeO₂ as a flame-retardant synergist, providing a foundation for developing fire-safe polymeric materials. Full article

Cellulose, as a green and renewable polymer material, has attracted the attention of a wide range of scholars for its excellent mechanical strength, easy chemical modification and degradability. However, its flammability limits its application in automotive, aerospace, construction, textile and electronic fields. This review recapitulates the modification methods of flame-retardant cellulose and their applications in polymers in recent years. This paper discusses the fabrication of flame-retardant cellulose from various aspects such as boron, nitrogen, phosphorus, sulphur, inorganic and heterogeneous synergistic modification, respectively, and evaluates the flame retardancy of flame-retardant cellulose by means of thermogravimetry, cone calorimetry, limiting oxygen index, the vertical combustion of UL94, etc. Finally, it discusses the application of flame-retardant cellulose in actual composites, which fully reflects the extraordinary potential of flame-retardant cellulose for applications in polymers. Currently, flame-retardant cellulose has significantly improved its flame-retardant properties through multi-faceted modification strategies and has shown a broad application prospect in composite materials. However, interfacial compatibility, environmental protection and process optimisation are still the key directions for future research, and efficient, low-toxic and industrialised flame-retardant cellulose materials need to be realised through innovative design. Full article

The inherent flammability and toxic smoke emission of epoxy resins (EPs) pose significant challenges to their advanced engineering applications. To address this limitation, we developed a novel flame-retardant additive through the organic modification of layered double hydroxides (LDHs) using a ternary MgAlLa hydrotalcite structure intercalated with phosphotungstic acid (PWA). This innovative design established a synergistic mechanism by combining the catalytic carbonization effect of lanthanum with the radical scavenging capability of PWA. The optimized MgAlLa-PWA/EP composite demonstrated remarkable flame retardancy and smoke suppression improvements, exhibiting 77.9% and 62.4% reductions in the peak heat release rate (pHRR) and total heat release (THR), respectively, compared to pure EP. Particularly noteworthy was the 72.6% decrease in total smoke release (TSR), accompanied by a significant elevation of the limiting oxygen index (LOI) value to 26.8% and achievement of UL-94 V-0 rating. Microstructural analysis revealed that the modified composite formed a continuous and uniform layer with increased density during combustion, effectively inhibiting oxygen exchange, smoke diffusion, and heat transfer. This study provides a novel strategy for designing multi-element synergistic LDHs additive for high-efficiency flame retardancy and smoke suppression of EP. Full article

Recent research has focused on developing environmentally friendly flame-retardant coatings to improve the fire resistance of wood. In this study, phytic acid–guanazole (PG), a dual-functional compound synthesized through an ionic reaction between phytic acid and guanazole, was added to KH550-modified urea–formaldehyde resin (KUF) as both a curing agent and flame retardant. The $-{\mathrm{PO}}_4^{3-}$ groups from phytic acid act as an acid source to accelerate char formation during combustion, while the −NH₂ groups introduced by guanazole release non-combustible gases to dilute oxygen in the air, synergistically enhancing flame retardancy. Additionally, the hygroscopic $-{\mathrm{PO}}_4^{3-}$ groups absorb free water in the resin, reducing the curing temperature and accelerating coating solidification. The KH550 coupling agent improves compatibility between KUF and PG while introducing silicon, which forms SiO₂ during combustion to strengthen the char layer and further enhance flame resistance. Evaluations showed that PG outperforms conventional tannic acid (TA) in curing efficiency and fire resistance. Comprehensive analyses, including Differential Scanning Calorimetry (DSC), Limiting Oxygen Index (LOI), vertical flame tests, and cone calorimetry, confirmed PG’s dual functionality. Scanning Electron Microscope (SEM) and Raman spectroscopy revealed that PG-modified coatings form denser post-combustion char layers, directly linked to improved fire resistance. As a multifunctional additive, PG eliminates the need for separate curing agents and utilizes bio-based phytic acid, offering cost-effective and sustainable advantages for industrial applications. Full article

Dimethyl methylphosphonate (DMMP) and modified nano-silica were utilised to enhance the mechanical properties, thermal stability, and flame retardancy of waterborne polyurethane (WPU). Nano-silica modified with the silane coupling agent γ-aminopropyltriethoxysilane (KH550) exhibited excellent dispersibility and stability. Compared with pure WPU, the limiting oxygen index (LOI) of P/Si-WPU increased from 18.1% to 28.3%, and its UL-94 rating reached V-0, with a significant improvement in elongation at break. Furthermore, the peak heat release rate of P/Si-WPU decreased by 29.1%, while the total heat release was reduced by 6.8% in comparison to pure WPU. The synergistic flame-retardant mechanism of phosphorus and silicon was investigated through an analysis of the char residue of WPU and its composites. This study provides a potential approach for the development of WPU with superior flame retardancy and enhanced mechanical properties. Full article

This study investigates the development of sustainable nanocomposites using recycled polyethylene terephthalate (RPET) and polyamide 11 (PA-11) blends reinforced with graphene nanoplatelets (GNPs). RPET/PA-11 blends were compatibilized with 2 phr Joncryl^® and processed using melt blending followed by injection moulding. The effects of varying GNP contents (1–4 phr) on mechanical, thermal, and flame-retardant properties were analysed. The nanocomposite with 1 phr GNPs exhibited an optimal balance of mechanical, flame-retardant, and thermal properties, along with improved dispersion compared to higher GNP loadings. Higher GNP concentrations led to increased stiffness but also promoted agglomeration, which negatively impacted tensile and impact strength. Thermal analysis revealed that GNPs influenced the cold crystallization behaviour of RPET, while the TGA results indicated a moderate enhancement in thermal stability. The maximum degradation temperature (T_max) increased from 410.38 °C to 430.06 °C with 1 phr GNPs but declined at higher loadings. Similarly, flammability tests showed an improvement in the limiting oxygen index (LOI) from 19 to 24. Morphological analysis confirmed that GNPs facilitated PA-11 dispersion within the RPET matrix, particularly at lower GNP concentrations (1 phr). These findings highlight the potential of RPET/PA-11/GNP nanocomposites for multifunctional applications, providing an optimal balance between mechanical performance, thermal stability, and flame resistance. This research highlights the synergistic effect of GNPs in achieving sustainable, high-performance materials, addressing the challenges of plastic waste management and the need for eco-friendly engineering solutions for industries such as automotive, packaging, and construction. Full article

In this study, fumed silica (FS) was used as a support material and infused with the hydrated salt sodium hydrogen phosphate dodecahydrate (DHPD) to create shape-stabilized constant phase change materials (CPCMs). These CPCMs were integrated into a polyurethane matrix as a functional filler, resulting in low-exothermic polyurethane composite foams (CPCM-RPUFs) that demonstrate thermoregulation and flame-retardant properties. Recent findings show that CPCM-RPUF excels in thermal stability compared to pure polyurethane, with a melt phase transition enthalpy of 115.8 J/g. The use of fumed silica allows for the encapsulation of hydrated salts up to 87%, ensuring the structural integrity of the vesicles. As FS content in CPCMs increased, the internal temperature of the composite foam significantly decreased, showing excellent thermal regulation. Thermogravimetric analysis showed that the synergistic effect of DHPD and FS improved the thermal stability and flame retardancy of the composites. By monitoring the internal and surface temperature changes in the foam, it was verified that CPCMs can effectively alleviate heat accumulation during the curing process and reduce the core temperature (56.9 °C) and surface warming rate, thus realizing the thermal buffering effect. With the increase in FS content in CPCMs, the compressive strength of CPCM-RPUF can be maintained or even enhanced. This study provides a theoretical basis and technical support for the development of polyurethane composite foams with integrated thermal regulation and flame-retardant properties, which can have broad application prospects in the fields of building energy conservation, energy storage equipment, and thermal mine insulation. Full article

Polyurethane (PUR)-based artificial leathers are often used as interior materials in public area, making flame retardants (FRs) necessary. The mode of action of different FRs varies depending on the chemical class and the structure of the supplied material. Usually, FRs are designed for bulk materials like foams, e.g., for upholstery, the main application of PUR. However, in thin materials, FRs act differently, thus leaving the PUR without sufficient flame resistance. In this study, PUR films and artificial leathers were equipped with twelve commercially available, halogen-free FRs in various concentrations and combinations. Fire resistance was tested with LOI measurements, cone calorimetry, horizontal burning behavior, and thermogravimetric analyses. An organophosphorus FR proved to be the most suited for flame-resistant artificial leather. The LOI was increased from 20 to 24.2%, the peak heat release rate was reduced by about 30%, and the sample was self-extinguishing in horizontal burning behavior. Phosphinates and aluminum trihydroxide were the least efficient FRs. Combinations of bentonite with phosphorus-based FRs showed synergistic effects in reducing the probability of igniting the material. The results demonstrate that sufficient flame retardancy for PUR-based thin materials can be achieved with commercially available halogen-free FRs, paving the way for more sustainable and greener materials by substituting ecologically harmful and health-damaging FRs. Full article

This study explores the development of sustainable fire-resistant composites using a blend of recycled linear low-density polyethylene (rLLDPE) and low-density polyethylene (rLDPE) for construction applications. The incorporation of non-halogenated intumescent flame retardants (IFRs), specifically ammonium polyphosphate (APP) and melamine polyphosphate (MPP), was shown to enhance the flame retardance, thermal stability, and mechanical performance of these recycled polymer blends. IFRs were introduced at 5 wt.% and 10 wt.% concentrations, and their effects were evaluated using limiting oxygen index (LOI) testing and thermogravimetric analysis (TGA). Results showed that 10 wt.% APP and a combination of 5 wt.% APP with 5 wt.% MPP increased LOI values from 18.5% (neat polymer blend) to 21.2% and 22.4%, respectively, demonstrating improved fire resistance. Enhanced char formation, facilitated by IFRs, contributes to superior thermal stability and fire protection. TGA results confirmed higher char yields, with the rLLDPE/rLDPE/MPP5/APP5 composition exhibiting the highest residue (3.00%), indicating a synergistic effect between APP and MPP. Rheological and mechanical analysis showed that APP had more impact on viscoelastic behavior, while the combination of IFRs provided balanced mechanical properties despite a slight reduction in tensile strength. This research highlights the potential of recycled polyethylene composites in promoting circular economy principles by developing sustainable, fire-resistant materials for the construction industry, reducing plastic waste, and enhancing the safety of recycled polymer-based applications. Full article

Developing eco-friendly, high-performance adhesives is crucial for sustainable industrial applications but remains a significant challenge. Herein, a synergistic strategy combining core–shell hybridization and borate chemistry was employed to fabricate a multifunctional soy protein (SPI) adhesive with excellent adhesion. Specifically, a reactive core–shell hybrid (POSS-U) was synthesized via free-radical polymerization using octavinyl-POSS as the core and urushiol (U) as the shell. Sodium borate (SB) was then added as a crosslinker, along with POSS-U and SPI, to prepare the SPI/POSS-U/SB adhesive. The SPI/POSS-U/SB adhesive exhibited a 100% increase in dry shear strength (2.46 MPa) and a wet shear strength of 0.74 MPa, meeting indoor application standards. Due to the thermal shielding and char formation of POSS and SB, the peak heat release rate of the modified adhesive reduced by 25.4%, revealing excellent flame retardancy. Additionally, the modified adhesive remained mold-free for 144 h due to the antifungal properties of urushiol and boron. This work provides an innovative approach for enhancing protein-based adhesives and contributes to the advancement of multifunctional composite materials. Full article

Pure phase change materials (PCMs) have drawbacks such as low thermal conductivity and poor physical properties like flammability, which limit their further application in battery thermal management systems. This paper introduces an innovative flame-retardant composite phase change material (CPCM) made from paraffin, expanded graphite, chitosan (CS), ammonium polyphosphate (APP), and aluminum hypophosphite (AHP). The physicochemical properties and flame-retardant performance of CPCMs with five different flame-retardant ratios of 9%, 12%, 15%, 18%, and 21% are studied, and their application effects in battery thermal safety are revealed. The results show that the combination of flame retardants CS, APP, and AHP exhibits effective synergistic effects, and the prepared CPCM exhibits good flame-retardant properties and thermal management effects. The CPCM exhibits outstanding thermal management performance when the flame-retardant content is 12%. At a maximum discharge rate of 3C, compared to natural air-cooling conditions, the maximum battery temperature and temperature difference are controlled within the safe range of 41 °C and below 5 °C, respectively. The CPCM can play an important role in the thermal safety of lithium-ion batteries. Full article

The issue of hazardous smoke and toxic gases released from epoxy resins (EP), which often causes casualties in real fires, has limited its application. Therefore, we have developed a novel flame retardant based on a bimetallic-doped phytate-melamine (BPM) structure with Zn²⁺ and Fe²⁺ ions incorporated into the polymer matrix using a straightforward solution-based synthetic method. The combustion performance of the composite was evaluated using a cone calorimeter test, which showed that the peak heat release, total heat release, and total smoke production were reduced by 50%, 31.7%, and 29.2%, respectively, compared to those of EP. Additionally, the fire growth index was noticeably reduced by 60% owing to the synergistic catalytic effect of the bimetallic ions, and the high nitrogen and phosphorus content of the additives. Overall, this study provides new insights into the application of bimetallic doping for flame retardant polymer composites. Full article