Search Results (253)

Halogenated flame retardants have been amongst the most widely used and effective solutions for enhancing fire resistance. However, their use is currently strictly regulated due to serious health and environmental concerns. In this context, phosphorus-based and mineral flame retardants have emerged as promising alternatives. Despite this, their combined use is neither straightforward nor guaranteed to be effective. This study scrutinizes the interactions between these two classes of flame retardants (FR) through a systematic analysis aimed at elucidating the antagonistic pathways that arise from their coexistence. Specifically, this study focuses on two inorganic fillers, mineral huntite and chemically precipitated magnesium hydroxide, both of which produce basic oxides upon thermal decomposition. These fillers were incorporated into a poly(butylene terephthalate) (PBT) matrix to be utilized as advanced-mattress FR coating fabric and were subjected to a series of flammability tests. The pyrolysis products of the prepared polymeric composite compounds were isolated and thoroughly characterized using a combination of analytical techniques. Thermogravimetric analysis (TGA) and differential thermogravimetric analysis (dTGA) were employed to monitor decomposition behavior, while the char residues collected at different pyrolysis stages were examined spectroscopically, using FTIR-ATR and Raman spectroscopy, to identify their structure and the chemical reactions that led to their formation. X-ray diffraction (XRD) experiments were also conducted to complement the spectroscopic findings in the chemical composition of the resulting char residues and to pinpoint the different species that constitute them. The morphological changes of the char’s structure were monitored by scanning electron microscopy with energy dispersive X-ray spectroscopy (SEM-EDS). Finally, the Limited Oxygen Index (LOI) and UL94 (vertical sample mode) methods were used to assess the relative flammability of the samples, revealing a significant drop in flame retardancy when both types of flame retardants are present. This reduction is attributed to the neutralization of acidic phosphorus species by the basic oxides generated during the decomposition of the basic inorganic fillers, as confirmed by the characterization techniques employed. These findings underscore the challenge of combining organophosphorus with popular flame-retardant classes such as mineral or basic metal flame retardants, offering insight into a key difficulty in formulating next-generation halogen-free flame-retardant composite coatings. Full article

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 oil and gas industry is subject to significant fire hazards due to the flammability of hydrocarbons and the extreme conditions of operational facilities. Intumescent coatings (ICs) serve as a crucial passive fire protection strategy, forming an insulating char layer when exposed to heat, thereby reducing heat transfer and delaying structural failure. This review article provides an overview of recent developments in the effectiveness of ICs in mitigating fire risks, enhancing structural resilience, and reducing environmental impacts within the oil and gas industry. The literature surveyed shows that analytical techniques, such as thermogravimetric analysis, scanning electron microscopy, and large-scale fire testing, have been used to evaluate the thermal insulation performances of the coatings. The results indicate significant temperature reductions on protected steel surfaces that extend critical failure times under hydrocarbon fire conditions. Recent advancements in nano-enhanced and bio-derived ICs have also improved thermal stability and mechanical durability. Furthermore, numerical modeling based on heat transfer, mass conservation, and kinetic equations aids in optimizing formulations for real-world applications. Nevertheless, challenges remain in terms of standardizing modeling frameworks and enhancing the environmental sustainability of ICs. This review highlights the progress made and the opportunities for continuous advances and innovation in IC technologies to meet the ever-evolving challenges and complexities in oil and gas industry operations. Consequently, the need to enhance fire protection by utilizing a combination of tools improves predictive modeling and supports regulatory compliance in high-risk industrial environments. Full article

Polyamide 6,6 (PA6,6) fabrics are widely used in textiles due to their high mechanical strength and chemical stability. However, their inherent flammability and melting behavior under fire pose significant safety challenges. In this study, a dual-layer flame-retardant system was developed by integrating atomic layer deposition (ALD) of ZnO with a phosphorus–silane-based flame retardant (DOPO-ETES). ALD allowed precise control of ZnO layer thickness (50, 84, and 199 nm), ensuring uniform coating. Thermal analysis (TGA) and microscale combustion calorimetry (MCC) revealed that ZnO altered the degradation pathway of PA6,6 through catalytic effects, promoting char formation and reducing heat release. The combination of ZnO and DOPO-ETES resulted in further reductions in heat release rates. However, direct flame tests showed that self-extinguishing behavior was not achieved, emphasizing the limitations related to the melting of PA6,6. TG-IR and cone calorimetry confirmed that ZnO coatings suppressed the release of smoke-related volatiles and incomplete combustion products. These findings highlight the potential of combining metal-based catalytic flame retardants like ZnO with phosphorus-based coatings to improve flame retardancy while addressing the specific challenges of polyamide textiles. This approach may also be adapted to other fabric types and integrated with additional flame retardants, broadening its relevance for textile applications. Full article

Fire-resistant coatings have emerged as crucial materials for reducing fire hazards in various industries, including construction, textiles, electronics, and aerospace. This review provides a comprehensive account of recent advances in fire-resistant coatings, emphasizing environmentally friendly and high-performance systems. Beginning with a classification of traditional halogenated and non-halogenated flame retardants (FRs), this article progresses to cover nitrogen-, phosphorus-, and hybrid-based systems. The synthesis methods, structure–property relationships, and fire suppression mechanisms are critically discussed. A particular focus is placed on bio-based and waterborne formulations that align with green chemistry principles, such as tannic acid (TA), phytic acid (PA), lignin, and deep eutectic solvents (DESs). Furthermore, the integration of nanomaterials and smart functionalities into fire-resistant coatings has demonstrated promising improvements in thermal stability, char formation, and smoke suppression. Applications in real-world contexts, ranging from wood and textiles to electronics and automotive interiors, highlight the commercial relevance of these developments. This review also addresses current challenges such as long-term durability, environmental impacts, and the standardization of performance testing. Ultimately, this article offers a roadmap for developing safer, sustainable, and multifunctional fire-resistant coatings for future materials engineering. Full article

Durable polyamidoamine (PAA) coatings were covalently grafted onto cotton by applying a water-soluble, glycine-based PAA (M-GLY) through a radical polymerization mechanism. M-GLY oligomers of different chain lengths, terminated with bisacrylamide groups, were synthesized via polyaddition of N,N′-methylenebisacrylamide and glycine at molar ratios of 1:0.9, 1:0.85, and 1:0.8. Cotton strips were then impregnated with differently concentrated (10 and 20 wt.%) aqueous solutions of the M-GLY oligomers in the presence of potassium persulfate, which oxidized cellulose and generated radicals that initiated polymerization of the M-GLY terminals, thereby enabling covalent grafting onto cotton. This process yielded M-GLY-grafted cotton (COT-g-M-GLY) with 2–15% add-on levels. Scanning electron microscopy revealed uniform surface coverage and penetration of the coating into fiber interiors. Grafting did not alter cellulose crystallinity—65% vs. 64% for grafted and virgin cotton. However, thermogravimetric analysis showed that COT-g-M-GLY exhibited lower thermo-oxidative stability than M-GLY-adsorbed cotton (COT/M-GLY) at similar add-ons. Flame-retardancy tests indicated that COT-g-M-GLY reduced the burning rate (by 10% to 30%) but did not achieve self-extinguishing behavior, unlike COT/M-GLY. Despite this, COT-g-M-GLY provided good protection against UV-induced photodegradation. After accelerated UVA–UVB exposure, cotton samples with 10% M-GLY add-on showed a significantly reduced yellowing rate compared to untreated cotton, as confirmed by spectrophotometric analysis. 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

With the increasing urgency of petroleum resource scarcity and environmental challenges, the development of degradable bio-based flame retardants has become crucial for enhancing the fire safety of organic materials. In this work, a phosphorus-containing chitosan derivative (CS-PPOA) was synthesized via a one-step protonation reaction between chitosan (CS) and phenylphosphinic acid (PPOA) under mild conditions. The resulting multifunctional flame-retardant coating was applied to polyester (PET) fabrics. Comprehensive characterization using FT-IR, XPS, and NMR confirmed the successful protonation of chitosan amino groups through electrostatic interactions, forming a stable ionic complex. The CS-PPOA solution exhibited excellent rheological properties and film-forming ability, producing films with over 80% optical transmittance and flexibility. Thermogravimetric analysis (TGA) revealed that CS-PPOA achieved char residue yields of 76.8% and 40.2% under nitrogen and air atmospheres, respectively, significantly surpassing those of acetic acid-protonated chitosan (CS-HAc). The limiting oxygen index (LOI) of CS-PPOA increased to 48.3%, and vertical burning tests demonstrated rapid self-extinguishing behavior. When applied to PET fabrics at a 15% loading, the LOI value improved from 20.3% (untreated fabric) to 27.8%, forming a dense char layer during combustion while completely suppressing melt dripping. Additionally, the coated fabric exhibited broad-spectrum antibacterial activity, achieving a 99.99% inhibition rate against Escherichia coli and Staphylococcus aureus. This study provides a novel strategy for the green and efficient preparation of multifunctional bio-based flame-retardant coatings. Full article

In this study, a solvent-free, slow-curing, inherently flame-retardant polyurea coating was successfully developed through an optimized formulation. The novel polyurea was synthesized using mixed Schiff base latent curing agents derived from terminal polyether amines with different-number average molecular weights (D2000 and D400), methyl isobutyl ketone, and polyethyl phosphate glycol ester (OP550). Subsequently, polyurea/meta-aramid (PUA/AF) composite fabrics were fabricated via a scraping coating technique. Thermogravimetric analysis revealed enhanced char formation and reduced decomposition temperatures due to the incorporation of OP550. Comprehensive flame retardant performance was demonstrated through vertical flame testing, limiting oxygen index, and micro-scale combustion calorimetry, with results showing significantly reduced heat release rates, lower total heat release, and increased residual char. Mechanical evaluations indicated marked improvements in tearing, tensile, single-yarn tensile, and bursting forces, attributed to strong fiber–polyurea interfacial interactions, as confirmed by detailed SEM morphological analyses. Moreover, the PUA/AF composites exhibited excellent static puncture resistance and effective self-healing capability. Collectively, these advancements highlight the potential of PUA/AF composite fabrics as promising candidates for advanced protective textiles, integrating superior flame retardancy, mechanical strength, puncture resistance, and self-repairing functionality. Full article

The Wan’an Bridge, the longest wooden lounge bridge in China with a history of more than 900 years, was devastated by a catastrophic fire in 2022. This tragic event underscores the susceptibility of historical wooden structures to fire damage. In this article, the bridge’s intricate structure and the development of the fire incident are introduced in detail. To gain a deeper insight into the patterns of fire propagation across the bridge and assess the reliability of fire simulations in predicting fire spread in historical wooden structures, we utilized the Fire Dynamics Simulator (FDS), with a sophisticated pyrolysis model and thermal response parameters specifically tailored to ancient fir wood. The modeling results reveal that the FDS simulation reflects the actual fire spread process well. Both the investigation and simulation findings indicate that once the flame reaches above the bridge deck, it enters a rapid three-dimensional propagation phase that is exceptionally challenging to control. Furthermore, the modeling results suggest that the application of intumescent fire-retardant coatings can significantly delay fire spread, reduce heat release rates, and suppress smoke production, thereby making them an effective fire prevention measure for historical wooden buildings. 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

This review explores the structural and electrochemical characteristics of carbon materials derived from polybenzoxazines, emphasizing their potential in supercapacitors. A detailed analysis of thermal degradation by-products during carbonization reveals distinct competing mechanisms, underscoring the exceptional thermal stability of benzoxazines. These materials exhibit significant pseudocapacitive behavior and excellent charge retention, making them strong candidates for energy storage applications. The versatility of polybenzoxazine-based carbons enables the formation of diverse morphologies—nanospheres, foams, films, nanofibers, and aerogels—each tailored for specific functionalities. Advanced synthesis techniques allow for precise control over porosity at the nanoscale, optimizing performance for supercapacitors and beyond. Their exceptional thermal stability, electrical conductivity, and tunable porosity extend their utility to gas adsorption, catalysis, and electromagnetic shielding. Additionally, their intumescent properties (unique ability to expand when exposed to high heat) make them promising candidates for flame-retardant coatings. The combination of customizable architecture, superior electrochemical performance, and high thermal resistance highlights their transformative potential in sustainable energy solutions and advanced protective applications. Full article

Enhancing the thermal resistance of carbon fiber-reinforced polymers (CFRPs) with flame retardants or coatings often leads to increased weight and reduced mechanical integrity. To address these challenges, this study introduces an innovative approach for developing nanocomposites using carbon-based nanoparticles, while preserving the structural lightweight properties. For this, carbon black particles (CBPs) up to 10% and carbon nanotubes (CNTs) up to 1.5% were incorporated into the RTM6/G939 composite material. The obtained samples were then analyzed for their properties and heat resistance under one-sided thermal loading at a heat flux of 50 kW/m². Results demonstrate that integrating these particles improves heat conduction without compromising the material’s inherent advantages. As a result, thermo-induced damage and the resulting loss of mechanical strength are delayed by 17% with CBPs and 7% with CNTs compared to the unmodified material. Thereby, the thermal behavior can be accurately modeled by a straightforward approach, using calibrated, effective measurements of the nanoparticles in the polymer matrix rather than relying on theoretical assumptions. This approach thus provides a promising methode to characterize and improve thermal resistance without significant trade-offs. Full article

An advanced, eco-friendly, and fully bio-based flame retardant (FR) system has been created and applied to the cellulose structure of the cotton fabric through a layer-by-layer coating method. This study examines the flame-retardant mechanism of protein-based and phosphorus-containing coatings to improve fire resistance. During combustion, the phosphate groups (−PO₄²⁻) in phosphorus containing flame retardant layers interact with the amino groups (–NH₂) of protein, forming ester bonds, which results in the generation of a crosslinked network between the amino groups and the phosphate groups. This structure greatly enhances the thermal stability of the residual char, hence improving fire resistance. Cone calorimeter and flammability tests show significant improvements in fire safety, including lower peak heat release rates, reduced smoke production, and higher char residue, all contributing to better flame-retardant performance. pHRR, THR, and TSP of the flame-retarded cotton fabric demonstrated 25, 54, and 72% reduction, respectively. These findings suggest that LbL-assembled protein–phosphorus-based coatings provide a promising, sustainable solution for creating efficient flame-retardant materials. Full article

Ultra-high-molecular-weight polyethylene (UHMWPE) fabric is widely used in many fields due to its excellent properties such as high modulus, high strength, and impact resistance. However, its high flammability prevents its application in high-temperature environments. Therefore, it is important to develop multifunctional UHMWPE fabric to meet its different requirements in firefighting, military, and other scenarios. Here, we have prepared a durable flame-retardant superhydrophobic UHMWPE fabric by a simple coating method. A polyurethane solution mixed with decabromodiphenylethane and antimony trioxide is scraped on the surface of the fabric to form a coating, which endows the fabric with flame retardancy. The sprayed fluorinated hydrophobic agent provides superhydrophobic properties to the fabric. It is worth mentioning that plasma pretreatment greatly improves the adhesion properties of the coating by stimulating the active groups on the surface of the fabric. Tests have shown that the adhesion between the coating and the surface of the plasma-treated UHMWPE fabric has been greatly improved. The limiting oxygen index value of the coating UHMWPE fabric has increased by 90%, and it immediately extinguishes after leaving the flame, demonstrating excellent flame retardancy. The contact angle between its surface and water reaches 156°, exhibiting excellent superhydrophobicity and self-cleaning properties. This study provides a simple, convenient, and effective method for the development of multifunctional UHMWPE fabric, greatly expanding its application scenarios and providing ideas for future development. Full article