Eco-friendly methylcellulose/zinc alginate film with multi-function properties: thermal stability, flame retardancy and antibacterial activities.

The purpose of this study was to synthesize crosslinked films from methylcellulose (MC) and sodium alginate (SA) using a straightforward ion exchange technique in a ZnCl2 coagulation bath. The resulting MC/ZA blend films exhibited significant improvements in thermal stability, with a measured increase of 191 °C in degradation temperature compared to MC film. The introduction of zinc ion (Zn2+) enhanced the flame retardancy of MC/ZA film, achieving a 92.4 % reduction in flammability. The microstructure of the MC/ZA blend film displayed a relatively smooth surface, indicating better biocompatibility between MC and ZA. Additionally, the barrier property of the MC/ZA film was improved, with a 35 % reduction in permeability to water vapor, and the mechanical properties were strengthened, showing a slightly reduction of 5 % in tensile strength. Furthermore, the MC/ZA blend film demonstrated enhanced antibacterial effectiveness, with a 99.99 % of S. aureus and E. coli, implying their suitability for packaging applications involving high oil content foods.

A Mussel-Inspired and Recyclable Coating with Integrated Daytime Radiative Cooling and Triboelectric Energy Harvesting for Intelligent and Sustainable Buildings.

Carbon neutrality necessitates new technologies for renewable energy utilization, active regulation of heat exchange, and material recycling to promote green and intelligent building development. Currently, the integration of these functions and characteristics into a single coating material presents a significant challenge. Here, we demonstrate a novel triboelectric and radiative cooling coating with mussel-inspired architectures, fabricated using cellulose nanofibers and Mica-TiO2 as a functional mortar and brick, respectively. The abundant polar groups and specific surface area of cellulose nanofibers enable a high accumulation of induced electrostatic charges, allowing the coating to act as a tribolayer to generate triboelectric outputs. The regularly layered arrangement of Mica-TiO2 endows fire resistance to the coating, which exhibits self-extinguishing properties and maintains 45% of its original electrical output even after direct exposure to flame for 20 s. Additionally, the created multilayered stacking morphology, as well as intense group vibrations of Mica-TiO2, facilitates high reflectivity (Rsolar = 0.9) and long-wave infrared emissivity (ϵLWIR = 0.94), achieving a daytime subambient temperature drop of 5.3 °C. Notably, the coating can be recycled easily while maintaining its triboelectric, radiative cooling, and fire-resistant properties. This work provides an innovative strategy for unifying triboelectric and radiative cooling functions, as well as recyclability, into a single coating material, offering new insights for future sustainable and energy-efficient buildings.

Lightweight, ultrahigh-strength and flame-retardant cellulose aerogel crosslinked with a reactive P/N-rich curdlan derivative.

Cellulose aerogel, recognized for its eco-friendliness, bio-sustainability and excellent thermal insulation property, holds immense potential as an insulation material. However, the application of cellulose aerogel has been hindered by its inherent drawbacks, particularly its low strength and flammability. In this study, a reactive P/N-rich curdlan derivative (NT) was synthesized and characterized. Lightweight, ultrahigh-strength and flame-retardant composite aerogels were then prepared by slow freezing, freeze-drying and chemical crosslinking methods. Composite aerogel crosslinked with 30% NT exhibited exceptional thermal insulation property with a low thermal conductivity of 33.9 mW/(m·K), which rivaled the value of petroleum-based thermal insulation materials. It possessed an ultrahigh compressive modulus (0.786 MPa) at low density (21.6 mg/cm3), which supported >12,000 times its weight. It also displayed superior flame-retardant property, with a limiting oxygen index of up to 33.1% and a V-0 rating in the UL-94 test. This study provides a new insight into the high-value utilization of natural polysaccharide and an innovative solution to the problem of low strength and flammability of cellulose aerogel. Cellulose aerogels with ultrahigh strength, superior flame retardancy and thermal insulation property possess a promising application in the fields of construction, aerospace and thermal protective clothing as high-performance thermal insulation materials.

Synergistic Effect of GO and MXene Enables Ultrasensitive, Reversible, and Self-Powered Fire Warning of a GO/MXene/Chitosan Aerogel.

Graphene oxide (GO)-based fire alarm materials have garnered extensive attention because the thermal reduction of GO to reduced GO (RGO) enables rapid fire warning. However, they suffer from poor flame retardancy, irreversible fire warning, and dependence on an external power supply. Herein, a GO/MXene/chitosan aerogel with a low density of 0.018 g cm-3 and good compressibility has been developed. The experimental results demonstrate that (i) MXene effectively reduces the peak and mean heat release rate of GO, while RGO nanosheets compensate for the structural instability of MXene in the flame due to thermal oxidation into TiO2; as such, long-lasting fire warning (>120 s) has been achieved; (ii) the reducibility and conductivity of MXene contribute to the ultrasensitive response of GO, with a fire response time of 1 s; and (iii) notably, the thermoelectric effect of MXene enables the reversible and self-powered fire warning of the GO/MXene/CS aerogel without an external power supply. Compared to pure MXene/CS aerogel, the presence of GO improves the sensitivity and stability of self-powered fire warning, owing to the formation of the highly conductive RGO nanosheets. The results of this work highlight the cooperation between GO and MXene in realizing ultrasensitive, long-lasting, reversible, and self-powered fire warning.

Eco-friendly flame retardant comprising chitosan-based effectively enhances the flame retardancy of wood with low weight percent gain.

Nowadays, there are many types of flame retardants, whether halogenated or halogen-free, that can improve the flame retardancy of wood. However, they continue to pose a significant threat to our environment and cause a substantial increase in the weight gain rates after treatment. It is highly desirable yet challenging to develop an eco-friendly and efficient flame retardant with low weight gain rates. Here, we report a simple and fast process for making eco-friendly flame retardants (chitosan, gelatin, sodium phytate and clay) with weight gain rates of 3.7 %, which form excellent flame retardancy systems. This method can be used to create a 53.5 % reduction in peak heat release rate (pHRR) an 189 % increase in ignition time (cone colorimeter), and a 71.9 % reduction in peak temperature (alcohol spray lamps) compared to raw wood. The results displayed that the effect of flame retardancy (Decreased ratio for pHRR/Weight percent gain) was the best in the past three years. In addition, the flame retardancy mechanism is thoroughly analyzed using the techniques of Raman and so on. This study proposes a novel strategy featured by eco-friendly and simple preparation process for enhancing the flame retardancy of wood in important areas.

Confined Polyethylene Glycol Anchored in Kaolinite as High Ionic Conductivity Solid-State Electrolyte for Lithium Batteries.

Solid-state electrolytes (SSEs) have garnered significant attention as critical materials for enabling safer, energy-dense, and reversible electrochemical energy storage in batteries. Among the various types of solid electrolytes developed, composite polymer electrolytes (CPEs) have stood out as some of the most promising candidates due to their well-rounded performance. In this study, we choose polyethylene glycol (PEG) as the covalent grafting intercalant and lithium perchlorate as carrier source to prepare a fast lithium ion conductor, K-PEG-Li doped with clay-based active filler as a CPE. The CPE exhibits excellent lithium conduction (4.36 × 10-3 S cm-1 at 25 °C and 3.32 × 10-2 S cm-1 at 115 °C), great mechanical performance with good tensile strength (6.07 MPa) and toughness (strain 313%), and convincing flame-retardancy. These outstanding conducting and mechanical functionalities indicate that such a clay-based active filler doped composite polymer electrolyte will find promising application in solid-state lithium batteries.

CoFe Oxides-Coated 2D Black Phosphorus for Flame-Retardant Nanocoatings with Tunable Mechanical Strength and Efficient Elimination of Toxic Gases.

2D black phosphorus (BP) degrades irreversibly into phosphate compounds under ambient conditions, which limits its application in a variety of fields. In this study, by coating amorphous ferric-cobalt oxides (CoFeO) on BP nanosheets, a multifunctional CoFeO@2D BP is successfully developed that effectively inhibited combustion and catalyzed CO oxidation to eliminate toxic gases. Strong affinity between transition-metal cations and BP allowed the uniform growth of amorphous ferric‒cobalt oxides on the BP surface, which effectively prevented the spontaneous degradation of 2D BP. By combining CoFeO@2D BP with gelatin and kosmotropic salts, the as-obtained nanocoatings are used for surface treatment of flammable polyurethane foam (PU). Kosmotropic ions induced strong hydrophobic interactions and bundling within the gelatin chains which significantly enhanced the mechanical performance of the PU. BP accelerates the carbonization of gelatin to inhibit the combustion of PU, and CoFe oxides, which act as true active centers to accelerate the oxidation of CO, effectively inhibiting the production of harmful gas. The release rate of CO decreases by 73% and the limiting oxygen index (LOI) increases from 17% to ≈32% during PU combustion. The developed novel 2D material opens the way for multifunctional coatings with integrated durability, flame retardancy, and high smoke suppression efficiency.

Biomass-inspired fabrication of eco-friendly, durable flame retardant and ultraviolet resistant lyocell fabric.

The pursuit of environmental friendliness, efficiency, and durability is paramount in the realm of flame retardant textile modification. Therefore, an innovative approach was designed to develop a gallic acid-derived intumescent flame retardant (GADPP), which contained reactive (-P(=O)(O-NH4+)2) and (-P(=O)(OCH2CH3)2) groups, facilitating functional modification of lyocell fabric. The GADPP modification effectively improved both flame retardancy and ultraviolet (UV) resistance of lyocell fabric. Fourier transform infrared spectroscopy, X-ray photoelectron spectroscopy, and scanning electron microscopy has substantiated the uniform distribution and covalent bond grafting of GADPP onto the fabric. Remarkably, even after 50 laundering cycles (LCs), the limiting oxygen index and UV protection factor values of lyocell fabric modified with 30 wt% GADPP remained at 29.8 % and 117.69, respectively. These results highlighted the synergistic effect of GADPP on enhancing the flame retardancy and UV resistance of lyocell fabric. Furthermore, this multi-functional modification strategy provides a sustainable path for the enduring enhancement of flame retardant and UV protective properties in lyocell fabrics.

Anti-flammable, anti-fouling, anti-bacterial treatment of cotton fabrics with MOF-based hybrid coatings for highly efficient oil-water separation.

A flame-retardant and hydrophobic coating was deposited on the surface of the cotton fabric via a two-step spray deposition technique. Specifically, the coating was composed of flame-retardant component (guanidine phosphate) and hydrophobic components (Ti-MOF and bis(3-aminopropyl)-terminated poly(dimethylsiloxane) (PDMS)) and crosslinked with glutaraldehyde. The limiting oxygen index (LOI) of the coated cotton fabrics increased from 18.0 % to 32.0 % (15#) and 26.5 % (15#-Ti-PDMS) relative to that of the original cotton fabric, and the coated cotton fabrics also self-extinguished in the UL-94 flammability test. Compared with that of the original cotton fabric, the PHRR of the coated fabrics was significantly lower, reaching 80 %. The coated cotton fabrics (15# and 15#-Ti-PDMS) had good antibacterial properties against Staphylococcus aureus (S. aureus). In addition, 15#-Ti-PDMS had high hydrophobicity, good washing and abrasion resistance and good water-oil separation performance. Its water contact angle was 146°. The water contact angle remained above 130° after 10 laundering cycles and 50 scratch cycles. Even under strongly acidic and strongly basic conditions, the water-oil separation efficiency of 15#-Ti-PDMS was greater than 99 %, and it was still greater than 90 % after 10 cycles. Therefore, a simple and effective method for preparing flame-retardant, hydrophobic and antibacterial cotton fabric was developed.

Facile Synthesis of Bis-Diphenylphosphine Oxide as a Flame Retardant for Epoxy Resins.

A phosphorus-containing compound, (oxybis(4,1-phenylene))bis(phenylphosphine oxide) (ODDPO), was successfully synthesized and used as a flame retardant for epoxy resin (EP). The results demonstrated that EP/ODDPO, containing 1.2 wt% phosphorus, achieved a vertical burning V-0 rating, with a limited oxygen index value of 29.2%, indicating excellent flame retardancy. Comprehensive evaluations revealed that ODDPO exhibited both gas-phase and condensed-phase flame-retardant effects on EP, with a particularly notable barrier effect. In addition, the incorporation of ODDPO had a minimal negative impact on the glass transition temperature (Tg) and thermal stability of the EP matrix. Compared to unmodified EP (EP-0), the Tg value and initial decomposition temperature of EP/ODDPO-1.2 decreased by only 7.6 °C and 10.0 °C, respectively. Moreover, the introduction of ODDPO significantly improved the hydrophobicity and water absorption resistance of epoxy materials, which is attributed to ODDPO's rigidity and symmetric structure, reducing water molecule permeation. Furthermore, the dielectric properties of ODDPO-modified EP samples were strengthened compared to EP-0, due to the ODDPO's symmetric structure reducing the polarity of the matrix. The above results indicated that ODDPO serves as an excellent flame retardant while enhancing other properties of the EP matrix, thereby contributing to the preparation and application of high-performance epoxy materials.

Sustainable lignosulfonate-modified PA6.6 fabrics to improve durable flame retardancy, hydrophilicity and mechanical performance.

Creating durable flame retardancy, enhanced mechanical performance, and hydrophilic polyamide 6.6 (PA6.6) textiles via cost-effectiveness from sustainable renewable sources is a considerable challenge. This study introduces a pretreatment process involving the application of sodium lignosulfonate (LS) to the surface of PA6.6 fabrics, thereby enhancing their hydrophilic and flame-retardant properties. Subsequently, a layer-by-layer (LbL) nanocoating treatment is employed, utilizing renewable polyelectrolytes-chitosan (CS), LS, and poly (sodium phosphate) (PSP)-to create 8-bilayer (BL) and 4-quarda layer (QL) structures that further improve the hydrophilicity and durable flame resistance of PA6.6 fabrics. The combined LS-modified and LbL coatings notably increased the limiting oxygen index (LOI) values from 19.5 % to 22.5 %, eliminated melt dripping, and secured a V-1 rating in the vertical burning (UL-94) tests. Moreover, the treated fabrics exhibited a 43 % reduction in the peak heat release rate (PHRR) and a lower fire growth rate (FGR) of 0.84 W/g·s, with a significant increase in char yield% in both air and nitrogen (N2) atmospheres. A cross-linked network structure is responsible for the superior hydrophilicity, enhanced tensile strength, and fabric softening properties. The self-crosslinking of sulfur-containing radicals with amide units ensures an anti-dripping performance that can withstand up to 30 home laundering cycles, demonstrating remarkable washing durability. However, a convincing approach has been developed for sustainable and high-performance materials for the textile industry, and a simple LbL technique using renewable polyelectrolytes that have traditionally been utilized in water treatment and food processing has been developed.

Preparation of straw/PLA composites with excellent flame retardancy based on deep eutectic solvent sulfonation.

There have been numerous studies on flame retardant modification of natural fiber/PLA composite materials due to the demand for applications. However, the existing flame retardant modification methods mostly involve adding flame retardants, which have a negative impact on the mechanical properties. Based on this, this study aims to introduce sulfonic groups into the cellulose of straw fibers via modification with a sulfamic acid-based deep eutectic solvent (SDES), thereby achieving flame retardance without affecting the inherent mechanical properties of the composite material. The performance enhancement of DS/PLA is manifested in the following specific aspects: the LOI reaches 36.53 %, the thermal stability is improved from 7.8 % of the residual carbon of PS/PLA to 38.4 %, and the tensile modulus is increased by 69.5 %. The preparation scheme for straw/PLA composite materials in this study is simple, economical, and efficient, and the flame retardant performance of the composite material is excellent, providing valuable references for flame retardant modification of natural fiber/plastic composite materials.

Synthesis of a phosphorus-containing L-lactic acid-based flame-retardant plasticizer for simultaneously enhancing flexibility and flame retardancy of poly(lactic acid).

This work provides a straightforward strategy for synthesizing efficient bio-based flame-retardant plasticizers, offering promising prospects for flame-retardant flexible materials. Poly(lactic acid) (PLA) has garnered significant attention as an environmentally friendly polymer among numerous biodegradable materials. However, its high flammability and brittleness severely hinder its application in the field of electronics and electrical devices. To address these challenges, a bio-based flame-retardant plasticizer (EPDL) was designed and synthesized using renewable L-lactic acid, which significantly enhances the flexibility and flame retardancy of PLA. Incorporating 40 phr EPDL resulted in PLA achieving UL94 V-0 grade and a limiting oxygen index of 34.3 %, demonstrating excellent flame-retardant properties. Meanwhile, the peak of heat release rate and total heat release of PLA/EPDL blends exhibited a marked reduction by 23.1 % and 34.1 % compared to that of pristine PLA, respectively. The flame-retardant action mode of EPDL is the combination of gas phase and condensed phase action. Additionally, the introduction of 40 phr EPDL significantly enhanced the ductility of PLA, resulting in a substantial rise in the elongation at break of the PLA/EPDL to 181.8 %, which is approximately 52 times higher than neat PLA. Intriguingly, the crystallization performance of PLA was enhanced by the presence of EPDL.

Green synthesis of multifunctional bamboo-based nonwoven fabrics for medical treatment.

Medical nonwovens fabrics are pivotal materials in modern healthcare systems, and find extensively application in surgical gowns, masks, nursing pads, and surgical instrument packaging. As healthcare requirements evolve and medical technology advances, the demand for functional nonwoven medical devices is continuously increasing. In addition, numerous environmental challenges and the need to transition to a sustainable society have increased the popularity of studies on environmentally friendly multifunctional nonwoven materials prepared from biomass fibers. Therefore, in this study, ecofriendly bamboo fibers were used to fabricate multifunctional medical nonwoven materials with superhydrophobic, antibacterial, flame-retardant, and biocompatible properties. Specifically, ZIF-67 was grown in situ on natural bamboo cellulose fibers (BCFs) extracted from natural bamboo and coated with polydimethylsiloxane to construct an environmentally friendly and versatile nonwoven fabric. The treated nonwoven fabric exhibited superhydrophobicity with contact angle of 163° and possess excellent self-cleaning properties. The antibacterial activity of the samples was investigated by the plate-counting method; the results showed that the untreated BCFs did not exhibit antibacterial activity, whereas the treated bamboo nonwoven fabrics demonstrated significant antibacterial activity (p < 0.001), with an antibacterial rate of >99 % against Escherichia coli, Staphylococcus aureus, Pseudomonas aeruginosa, Bacillus subtilis, and Candida albicans. In addition, when the samples were exposed to different temperatures (-4 and 50 °C) and humidities (0 % and 95 %), they demonstrated an antibacterial activity of >99 % against E. coli (F5,10 = 0.602; p = 0.670) and S. aureus (F4,10 = 0.289; p = 0.879). The heat release rate and smoke production rate of the nonwoven fabric decreased by 54.64 % and 93.18 %, respectively, compared to those of the BCFs, indicating excellent flame retardancy. The nonwoven fabric also exhibited satisfactory biocompatibility and breathability, ensuring user comfortability. This research not only has significant implications for producing low-cost, environmentally friendly, sustainable, and multifunctional medical products and openi up new pathways for the diversified utilization of bamboo, thereby expanding its applicability.

Recent Advances in Fire-Retardant Silicone Rubber Composites.

Silicone rubber (SR), as one kind of highly valuable rubber material, has been widely used in many fields, e.g., construction, transportation, the electronics industry, automobiles, aviation, and biology, owing to its attractive properties, including high- and low-temperature resistance, weathering resistance, chemical stability, and electrical isolation, as well as transparency. Unfortunately, the inherent flammability of SR largely restricts its practical application in many fields that have high standard requirements for flame retardancy. Throughout the last decade, a series of flame-retardant strategies have been adopted which enhance the flame retardancy of SR and even enhance its other key properties, such as mechanical properties and thermal stability. This comprehensive review systematically reviewed the recent research advances in flame-retarded SR materials and summarized and introduced the up-to-date design of different types of flame retardants and their effects on flame-retardant properties and other performances of SR. In addition, the related flame-retardant mechanisms of the as-prepared flame-retardant SR materials are analyzed and presented. Moreover, key challenges associated with these various types of FRs are discussed, and future development directions are also proposed.

Fire-Resistant and Thermal Stability Properties of Fluorosilicone Adhesives by Incorporation of Surface-Modified Aluminum Trihydrate.

Fluorosilicone was combined with aluminum trihydrate (ATH) to induce synergistic flame-retardant and thermal-resistant properties. The surface of ATH was modified with four different silane coupling agents. The flammability and mechanical properties of the fluorosilicone/ATH composites were assessed using an UL94 vertical test and a die shear strength test. The change in shear strength was investigated under aging for 1000 h at -55 °C and 150 °C. Pure fluorosilicone had inherent fire resistance and thus achieved a V-0 rating even at 20 wt.% ATH loading. Upon addition of ATH treated with 3-glycidoxypropyl trimethoxysilane, the composites exhibited the highest shear strength of 3.9 MPa at 23 °C because of the additional crosslinking reaction of fluorosilicone resin with the epoxide functional group of the coupling agent. Regardless of the types of coupling agents, the composites exhibited similar flame retardancy at the same ATH content, with a slight reduction in shear strength at 180 °C and 250 °C. The shear strength of the adhesives gradually decreased with aging time at -55 °C, but increased noticeably from 3.9 MPa to 11.5 MPa when aged at 150 °C due to the occurrence of the additional crosslinking reaction of fluorosilicone.

Optimization Design of the Multidimensional Heterostructure toward Lightweight, Broadband, Highly Efficient, and Flame-Retarding Electromagnetic Wave-Absorbing Composites.

A novel multidimensional electromagnetic wave-absorbing material was developed by combining carboxylated carbon nanotubes (CNT) with graphene oxide (GO) through multidimensional design, and cobalt/nickel-based metal organic frameworks (Co/Ni-MOF) were subsequently loaded onto the GO surface via its rich functional groups to form the composite absorbing material CNT-rGO-Co/Ni-MOF. Incorporating 25 wt % of CNT-rGO-Co/Ni-MOF into the paraffin matrix led to a remarkable RLmin value of -43 dB at 16.4 GHz, with an effective absorbing bandwidth (EAB) exceeding 4 GHz, all within a thickness of just 1.5 mm, showcasing its "lightweight, broadband, and high efficiency" characteristics. The exceptional electromagnetic wave absorption performance was attributed to multi-interface polarization loss, resistance loss, and magnetic medium loss. Furthermore, when incorporating 10 wt % of CNT-rGO-Co/Ni-MOF, the heat release capacity and peak heat release rate of EP/CNT-rGO-Co/Ni-MOF10 decreased by 59.2 and 52.6%, respectively.

Full bio-based flame retardant towards multifunctional polylactic acid: Crystallization, flame retardant, antibacterial and enhanced mechanical properties.

The preparation of flame-retardant high-performance polylactic acid (PLA) composites by adding green flame retardants have always been a challenge. In this work, an intumescent flame-retardant PCR based on phytic acid, chitosan, and resveratrol was successfully designed. Adding 4 wt% of PCR, the PLA-PCR composite was classified as UL-94 V-0 grade, with a LOI value increasing from 19.7 % (pure PLA) to 26.0 %, a peak heat release rate decreasing from 433 to 344 kW/m2. Owing to excellent compatibility of PCR, the mechanical strength and toughness of PLA-PCR composites have been improved, as reflected by a ~ 16 % increase in tensile strength, a ~ 73 % increase in impact strength and a ~ 57 % increase in toughness. In addition, PCR also presented plasticization effect on PLA, making it easier to process. This work provided a highly efficient and environmental-friendly modification approach for the development of multifunctional polymers.

Facile fabrication of ultradurable flame-retardant and hydrophobic cotton fabric with P/N-rich maltodextrin derivative and octadecyltrimethoxysilane.

Flame-retardant and hydrophobic cotton fabric provides protections from fire, stain and bacteria in daily life. However, it is still a great challenge to achieve ultrahigh durability via a green and facile technology. Herein, we synthesized a reactive P/N-rich maltodextrin derivative (PM), and reported a facile dipping-baking strategy to fabricate ultradurable flame-retardant and hydrophobic cotton fabric with PM and octadecyltrimethoxysilane (OTMS). The acids released from PM not only reacted with cellulose during baking, but also catalyzed the hydrolysis-polycondensation of OTMS and silylation reaction of cellulose. Thanks to the P/N/Si synergy and the existence of polyalkylsiloxane coating, treated fabric exhibited outstanding flame retardancy and hydrophobicity with a limiting oxygen index (LOI) of 34.7% and a water contact angle (WCA) of 143.3°. The chemical crosslinkings in PM-cellulose and OTMS-cellulose imparted ultrahigh durability to treated fabric. The LOI and WCA of treated fabric still reached 27.2% and 127.9° after 50 harsh washing cycles, respectively. Moreover, the WCA still maintained above 125° after 3000 intense friction cycles or soaked in strongly acidic/alkaline solution for 3 days. This work not only provides a new idea to synthesize biobased reactive flame retardant, but also a feasible and sustainable strategy for fabricating ultradurable hydrophobic and flame-retardant cotton fabric.

Simultaneously Flame Retarding and Toughening of Epoxy Resin Composites Based on Two-Dimensional Polyhedral Oligomeric Silsesquioxane/Polyoxometalate Supramolecular Nanocrystals with Ultralow Loading.

For industrial practical applications, it is difficult to simultaneously endow epoxy resin (EP) composites with superior flame retardancy, smoke suppression, toughness, and low-dielectric constants. Herein, unique polyhedral oligomeric silsesquioxane/polyoxometalate (POM(Mo)-POSS(ibu-Li)) nanosheets were synthesized via a simple one-pot method using laboratory-made lithium-containing hepta-isobutyl-POSS (ibu-Li-POSS) and the low-cost industrial chromogenic agent H3PMo12O40 as raw materials. The incorporation of 2 wt % POM(Mo)-POSS(ibu-Li) nanoflakes into EP significantly enhanced the compatibility between nanoadditives and the EP matrix. Compared with EP, the flexural and impact strengths increased by 36.2 and 78.2%, respectively. Therefore, POM(Mo)-POSS(ibu-Li) has significant advantages in enhancing the toughness of EP compared with existing flame retardants. The dielectric constant and loss were apparently reduced to meet the increasing requirements of EP-type electronic packaging materials and components. Notably, the synthesized POM(Mo)-POSS(ibu-Li) contained various flame-retardant and smoke-suppression elements such as P, Mo, and Si. The ultralow loading (2 wt %) of POM(Mo)-POSS(ibu-Li) significantly reduced the peak heat release rate, peak of smoke production rate, and CO production rate by 43.9, 40.6, and 65.8%, respectively. Meanwhile, the value of LOI increased directly from 24.0% for EP to 30.2% and passed the V-0 rating in the UL-94 test. However, incorporating 5 wt % POSS derivatives into EP alone to ensure that the prepared composites pass the V-0 rating of the UL-94 test has always been an extraordinarily difficult problem. Therefore, the dilemmas of poor dielectric properties, inherent flammability, and brittleness of EP were completely overcome through the successful application of POM(Mo)-POSS(ibu-Li) supramolecular nanosheets.