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A plant derived bio-macromolecule namely lignin (L) and a green phosphorus compound like phytic acid (PA) were functionalized with graphene oxide (GO) and subsequently, used to enhance the flame retardant properties of polyamide 66 (PA66) fabrics in a one pot deposition method. Meanwhile, we also considered pure phytic acid and one more bio-derived charring agent like chitosan (CS) to formulate a series of GO-based flame retardant finishing by altering the applied compounds in the formulation. The applied finishing with a minimum loading % (i.e., less than 10%) rarely altered the physical properties (i.e., color, handle and tensile strength, etc.) of treated textiles while provided enhanced thermal stability and added flame retardancy. Thus, a significant increase in limiting oxygen index (LOI) by 27% was received for the GO-lignin and GO-phytic acid modified fabric sample (i.e., PA66-A), indicating the supremacy of graphene-based compound. Furthermore, a substantial reduction in the peak heat release rate (pHRR) by 25% was also noticed for the fabric sample treated with GO-lignin, chitosan and phytic acid (i.e., PA66-D). Additionally, the as prepared finishing exhibited a considerable level of wash durability as a maximum reduction of pHRR by 17% was retained even after 5 washing cycles. Unlabelled Image • GO-functionalized biomolecules were used in developing flame retardant PA66 fabric. • This treatment rarely altered the color, handle and tensile strength of PA66 fabric. • GO-lignin and GO-phytic acid treated PA66 fabric received a LOI of 27%. • PA66 treated with GO-lignin, chitosan and phytic acid showed 25% pHRR reduction. • These flame retardant and thermally stable coatings were wash-durable as well. [ABSTRACT FROM AUTHOR]

• Two different flame retardants named as DOPO-GPTMS and DOPO-APTES were synthesized. • Flame retardant compounds were applied to PA66 fabric surfaces via sol-gel method. • The as prepared coatings could able to stop the melt-dripping of PA66. • PA66 treated with 20 wt% DOPO-APTES showed a maximum 36% reduction in pHRR. • Incorporation of Si-compounds enhanced charring ability of DOPO. Two different DOPO- Alkoxysilane based flame retardant compounds were synthesized and applied onto the polyamide 66 (PA66) fabric surfaces via sol-gel method to improve the thermal stability and flame retardant properties. The as prepared coatings exhibited a much higher char yield% compared to the pure PA66 and simultaneously suppressed the dripping tendency of PA66 in the vertical burning test. The fabric sample modified with 20 wt% of DOPO-APTES showed a significant reduction in the peak heat release rate (pHRR) by 36%, whereas the 20 wt% of DOPO-GPTMS treated fabric sample could manage a 20% reduction in pHRR. The supremacy of DOPO-APTES treated fabrics were due to the co-presence of P, Si, and N elements; where a DOPO structure showed a quenching effect in a vapor phase, and Si-compounds accelerated the limited charring of DOPO in a condensed phase and stabilized the char residues in a higher temperature range. Moreover, the as treated PA66 fabrics show some sort of wash durability and among them, the fabric sample treated with 20 wt% of DOPO-APTES can withstand against fierce laundering where it maintains UL-94V-1 rating even after 10 washing cycles. [ABSTRACT FROM AUTHOR]

For improving the flame retardancy of epoxy resin (EP), β‐cyclodextrin@ ferrocene@hollow mesoporous silica microspheres (β‐CD@FE@HMS) were prepared successfully by the self‐assembly method. Then, they were used as flame retardant to improve the fire safety of EP. EP/β‐CD@FE and EP/HMS composites were also prepared for comparative study. The results showed that β‐CD@FE@HMS could effectively improve the thermal stability of EP, in which the initial degradation temperature and the amount of char residue of EP were increased. The content of small molecule toxic gases produced by the combustion of EP composite was also reduced apparently. With the addition of 5 wt% β‐CD@FE@HMS, LOI value of EP was increased to 27.5% from 19.8%, and UL‐94 reached V‐1 rating. Comparing with pure EP, the peak heat release rate and total heat release values of EP were reduced by 11.0% and 12.3%, respectively, and the total smoke production was reduced by 30.6%. EP/β‐CD@FE@HMS composite formed a higher quality char layer. Therefore, β‐CD@FE@HMS microspheres could improve the fire safety of EP. [ABSTRACT FROM AUTHOR]

Chitosan (CS) and phosphorylated chitosan (PCS) were deposited onto the polyamide 66 (PA66) fabric surfaces along with poly-acrylate sodium (PAS) via 'one pot' and layer by layer (LbL) assembly methods in preparing flame retardant coatings. Subsequently, to stabilize the deposited coatings, some of the fabric samples were treated under the UV-irradiation and additionally, a thermal treatment was also carried out for the remaining fabric samples. The LbL assembled fabrics showed a better homogeneity in the coating structure over the one pot deposited fabrics as appeared in scanning electron microscopy (SEM). Nonetheless, the LbL treated fabric sample (i.e., PA66-10BL-UV) with a higher weight gain% exhibited a greater improvement in limiting oxygen index (LOI) (i.e., 23%), and a reduced peak heat release rate (pHRR) (i.e., 25%). Yet more, only the LbL assembled and thermally cross-linked fabric sample could able to retain the flame retardant behavior in the vertical burning test even after 5 washing cycles. • A flame retardant coating for PA 66 textiles was developed from chitosan polymers • Coatings were constructed via one pot deposition and layer by layer assembly method • LbL assembled coatings exhibited a better homogeneity over one pot deposition • A maximal reduction of 25% in pHRR was achieved for LbL assembled fabric sample • LbL assembly showed superior flame retardancy over one pot deposited fabric samples [ABSTRACT FROM AUTHOR]

Simultaneous flame retardancy and tensile strength enhancement of poly(lactic acid) (PLA) is particularly important due to its eco-friendliness and potential application as an engineering plastic. This work investigates the application of azo-boron (AZOB) modified reduced graphene oxide (RGO) intercalated by sodium metaborate (SMB) for simultaneous flame retardant (FR), smoke/toxic fumes suppression and tensile strength enhancement of PLA nanocomposites. The RGO-AZOB/SMB hybrid was prepared by aryl grafting of AZOB on GO followed by in-situ reduction/intercalation with sodium borohydride/SMB. Then RGO-AZOB/SMB hybrid was incorporated into PLA, and the properties were examined. Cone calorimeter test demonstrates improved FR performance by substantial reductions in peak heat release rate ∼76.5%, total heat release ∼76.9%, total smoke release ∼55.6%, peak CO production ∼25.9% and peak CO 2 production by ∼78.6%. A V-0 rating was attained in the UL 94 test with a higher LOI value of 31.2%. Considerable reductions in pyrolysis products, mainly hydrocarbons, CO, CO 2 , and carbonyl compounds were observed. The tensile strength and Young's Modulus were improved by 49.1% and 34.9% respectively. The FR mechanism of RGO-AZOB/SMB/PLA nanocomposites is based primarily on the glassy charring effect of the B–OH groups in AZOB and the inherent lamellar blocking effect of RGO. Image 1 [ABSTRACT FROM AUTHOR]

Graphical abstract Highlights • A hierarchical MoS 2 @TiO 2 structure is firstly designed and synthesized. • The combination properties of BD with 2 wt% MoS 2 @TiO 2 loading is greatly enhanced. • The mechanism of MoS 2 @TiO 2 in enhancing combination properties of BD is proposed. Abstract Bismaleimide/diallyl bisphenol A (BD), a kind of allyl-modified bismaleimide (BMI) system, which is widely used in the fields of aviation, aerospace, machinery, and electronics. However, the further applications of BD are severely restricted by its high crosslink density, brittleness, and undesirable flammability. In order to overcome these drawbacks, a hierarchical MoS 2 @TiO 2 structure is designed and synthesized to improve the mechanical and fire safety of BD, which are well matched with the high curing temperature and application temperature of BD. Specifically, with a relatively low loading of 2 wt% MoS 2 @TiO 2 , then the peak heat release rate (pHRR) and total heat release (THR) of BD composites are 314.25 kW/m2 and 53.58 MJ/m2, respectively, which are decreased by 32.5% and 15.0% in comparison to those of the pristine BD. Meanwhile, the TSR and yields of poisonous gases, especially CO and nitric oxide of BD/MoS 2 @TiO 2 2.0 are greatly decreased which indicates that the fire safety is effectively enhanced. The impact strength of BD/MoS 2 @TiO 2 2.0 sample is increased to 12.44 kJ/m2, which corresponding to a 96.8% compared with that of pure BD, and its storage modulus is 44462 MPa, a little higher than that of pure BD. Furthermore, Tg of BD/MoS 2 @TiO 2 2.0 is increased to 326 °C with a lower cross-linking density while that of BD is 316 °C. Conclusively, this investigation demonstrates that the MoS 2 @TiO 2 is a significant nano-additive for developing high-performance BD resins with excellent fire safety and mechanical properties, which provides a novel strategy for designing advanced BD composite material. [ABSTRACT FROM AUTHOR]

[Display omitted] • A multifunctional additive (MCMH) is carefully designed. • The microencapsulation technology improves the compatibility between MCMH and XLEVA. • The OIT value of XLEVA/MCMH was basically unchanged after extracted for 5 days. • The retention of EB of XLEVA/MCMH could reach 71.8% after aging at 165 °C for 14 days. • The PHRR and Ds max of XLEVA/MCMH are reduced by 89.4% and 53.6%, respectively. A multifunctional additive is carefully designed for crosslinked ethylene–vinyl acetate copolymer (XLEVA) composites to improve their mechanical properties, aging resistance and fire safety. In this study, first, a layer of silica was microencapsulated on magnesium hydroxide to give a large amount of hydroxyl group on the magnesium hydroxide surface; second, the primary antioxidant 3-(3, 5-di- tert -butyl-4 hydroxyphenyl) propionicacid was grafted on SiMH surface to prepare antioxidant microencapsulated flame retardants (MCMH). Compared with the pure XLEVA, the peak heat release rate and the maximum smoke density of flame retardant XLEVA/MCMH are decreased by 89.46% and 53.6%, respectively. Moreover, these oxidation induction time values of XLEVA/MH/AO and XLEVA/SiMH/AO decreased sharply after extracted for 1d. However, the OIT value of XLEVA/MCMH was basically unchanged after extracted for 5d. After aging at 165 °C for 14 days and γ-ray irradiation dose of 500 kGy, the retention of elongation at break could reach 71.8% and 86.6%, showing excellent aging resistance. These results show that MCMH has a good synergistic effect for enhancing the flame retardant, mechanical property as well as aging resistance of XLEVA composites. The "Killing three birds with one stone" strategy provides an excellent solution for obtaining high-performance XLEVA cable materials. [ABSTRACT FROM AUTHOR]

Due to the inherent flammability of polypropylene (PP), it is limited in the application of flame retardant materials. In this work, a novel char forming agent, hyperbranched phosphorus-containing polyurethane (HPPU), was synthesized and used as efficient char forming agent. When ammonium polyphosphate (APP) was combined with HPPU, APP/HPPU endow PP significantly improved flame retardancy than single APP. Although the total carbon monoxide production (TCOP) of some PP/APP/HPPU composites is higher than that of PP/APP composite, it is still lower than that of neat PP. LOI (limited oxygen index) and UL-94 tests reveal that PP composites with 25 wt% HPPU/APP with ratio of 4:1 are able to reach 27 vol% and V-0 rating, respectively. The addition of 25 wt% APP/HPPU with ratio of 2:1 into PP can result in decrease in peak heat release rate of about 72%, decrease in total heat release of about 38% and decrease in TCOP of about 93%. APP/HPPU promotes PP to form more stable, compact, and continuous char layer which effectively hinder heat and oxygen transfer and protect the inner matrix from decomposition. Thermogravimetric-infrared results reveal that the gas phase flame retardant mechanism of APP/HPPU is the dilution effect of ammonia from APP and the flame inhibition effect of phosphorus-containing species from HPPU. Image 1 • A novel hyperbranched phosphorus-containing polyurethane (HPPU) is firstly synthesized. • LOI and UL-94 tests revealed that the addition of 25 wt % HPPU/APP into neat PP was able to reach 27 % and V-0 rating. • APP/HPPU exhibit remarkable flame retardant and carbon monoxide (CO) suppression to PP composites. [ABSTRACT FROM AUTHOR]

Finding a facile strategy to fabricate robust coating on the skeletons is crucial to improve the performance of flexible polyurethane foam (FPUF). Nanosized bimetal-organic frameworks (MOFs-NH 2) and (3-Mercaptopropyl) trimethoxysilane (MTS) were used to modify FPUF in this work to enhance its oil absorbency and flame retardancy. MTS used as adhesive to provide strong interaction between MOFs-NH 2 and FPUF. FPUF@MOFs-NH 2 showed superhydrophobicity even after compressive stain-stress test for 1000 cycles. Meanwhile, FPUF@MOFs-NH 2 sponges not only had higher oil absorbency than previous FPUF-based adsorbents, but also superior reusability. After 400 cycles adsorption-squeezing test, FPUF@MOFs-NH 2 still kept high absorbency. Fire safety of the sponge was significantly improved after coating MTS and MOFs-NH 2 : fire spread and heat release rate were significantly suppressed. The possible oil absorbency and flame retardancy mechanisms were proposed based on the analysis results. This work broadens the application field of MOFs and paves a new direction to prepare functional FPUF composites with excellent performance. Image 1 [ABSTRACT FROM AUTHOR]

Flame retardant flexible polyurethane foam (FPUF) was prepared through a free-foaming method with aluminum diethylphosphinate (ADP) as additive. The influence of ADP on the morphology, thermal and flame retardant properties of the FPUF was investigated, and the flame retardant mechanism was further explored. TGA results indicated that the addition of ADP slightly affected the initial degradation temperature and the maximum degradation temperature. With the increase of the ADP loading, the char yield of the resultant FPUF gradually increased. When the ADP loading was 20%, the peak heat release rate and the total heat release of the resultant FPUF was reduced by 35% and 33%, respectively, compared to the unmodified FPUF. The addition of ADP improved the char formation of the FPUF, which could inhibit the transfer of oxygen and flammable gases between the flame and the underlying polymer and thus improve the fire retardancy. • Influence of ADP loading on the flame retardant property of FPUFs was studied. • The presence of ADP almost did not affect the thermal stability of FPUF. • Addition of ADP decreased the peak heat release rate and total heat release of FPUF. • ADP functioned as flame retardant in both gas phase and condensed phase. [ABSTRACT FROM AUTHOR]

Rising concerns about the toxic effects and environmental issues associated with various fireproof treatments on textiles have led to a demand for "green" materials. Chitosan (CS) is an amino polysaccharide green, recyclable, and non-toxic highly biocompatible biopolymer that consists of multiple hydroxyl groups and has a wide range of applications, including as a flame retardant additive. In this study, an eco-friendly bio-based formaldehyde-free flame retardant containing a higher level of phosphorus and nitrogen in phytic acid ammonia (PAA) was synthesized to amplify the most plentiful green chitosan (CS)-modified polyamide 66 (PA66) fabric surface through a simple pad-dry-cure technique for the improvement of durable flame retardancy with hydrophilicity. The findings revealed that each UV-grafted CS fabric could entirely stop the melt-dripping tendency during the vertical burning (UL-94) test and reached a V -1 rating. Meanwhile, limiting oxygen index (LOI) testing showed a rapid increase from 18.5 % to 24 % for the PA66 control and the PAA-treated (i.e., PA66-g-5CS-PAA) fabric samples, respectively. Moreover, compared to the PA66 control sample, a dramatic decrease in the peak heat release rate (PHRR), fire growth rate (FGR), and total heat release (THR) by approximately over 52 %, 0.63 %, and 19.7 %, respectively, was observed for the PA66-g-5CS-PAA fabric sample. Additionally, this arrangement of PAA catalyzed the charring of grafted CS and acted as a condensed phase flame retardant, resulting in a significant improvement in char yield% in both air and N 2 atmospheres for the PA66-g-5CS-PAA fabric sample in TGA. In addition, only the lower grafting ratio of CS with PAA-treated fabric sample (i.e., PA66-g-2CS-PAA) could encourage it to gain its lowest water contact angle of 00, as well as impersonating a positive effect in improving the flame retardant coating durability in washing and sustaining even after 10 home laundering cycles. This phenomenon suggests that an actual hydrophilic and durable flame retardant finishing procedure for polyamide 66 fabrics might be applied with the novel, plentiful, sustainable, and environmentally friendly bio-based green PAA ingredient. [ABSTRACT FROM AUTHOR]

• A vanillin-derived bisDOPO co-curing agent (DVD) was successfully synthesized from vanillin and DOPO. • The introduction of DVD improved the mechanical properties of epoxy thermosets. • Epoxy with an ultra-low P content of 0.42 wt% exhibited an LOI of 30.5% and reached a UL-94 V-0 rating. To prepare transparent and flame-retardant epoxy thermosets, a vanillin-derived bisDOPO co-curing agent (DVD) was synthesized from vanillin and DOPO. The influence of DVD on the curing kinetics of the epoxy systems was investigated by non-isothermal differential scanning calorimetry (DSC). The introduction of DVD increased the activation energy of the curing process. Compared with pure epoxy, the storage modulus at 30 °C and tensile strength of EP/DVD-5% increased by 35.7% and 145%, respectively. Additionally, the epoxy thermosets still maintained excellent transparency. The addition of DVD improved the flame-retardant performance of epoxy thermosets by promoting the formation of char and reducing the thermal decomposition rate. Most importantly, DVD showed high flame retardant efficiency for the resulting epoxy thermosets. Specifically, with the incorporation of 5 wt% DVD (only 0.42 wt% phosphorus loading), the resulting epoxy thermoset exhibited a limiting oxygen index (LOI) value of 30.5% and reached a UL-94 V-0 rating. The cone calorimetry results showed that the total heat release (THR), peak value of heat release rate (PHRR), and total smoke production (TSP) of EP/DVD-5% decreased by 32%, 42%, and 21%, respectively, compared with the unmodified EP. The modes of action of flame retardant analysis indicated that DVD exhibited high flame retardant efficiency by serving as a charring promotor in the condensed phase and acting as a radical scavenger in the gaseous phase. The above results demonstrate that DVD is a promising flame retardant agent to render epoxy thermosets simultaneously improved flame retardancy, mechanical strength and transparency. [ABSTRACT FROM AUTHOR]

In this work, a flowering-branch like CNTs/Bi 2 Se 3 hybrids was synthesized by a facile in-situ method. CNTs as carrier could provide low agglomeration of layered Bi 2 Se 3 . As-prepared nanomaterials were added into epoxy resin (EP) to enhance its fire safety. Compared with neat EP, there were more than 44% and 23% decrease in the value of peak heat release and total heat release with 2 wt% content of CNTs/Bi 2 Se 3 , respectively, confirmed the enhancement of flame retardancy of EP composites. Meanwhile, the release of smoke and CO were also suppressed during EP combustion. From results of thermogravimetric analysis-infrared spectrometry, the addition of CNTs/Bi 2 Se 3 obviously reduced the release of organic gaseous products, which contributed to the improved fire safety of EP matrix. Based on the analysis of gas and condensed phases, the possible enhancement mechanisms can be mainly concluded as the barrier effect of as-synthesized binary hybrids and enhanced char layers. Meanwhile, the addition of CNTs/Bi 2 Se 3 enhanced the mechanical performance of EP composites. This work broadens the application fields of Bi 2 Se 3 and enriches the membership of CNTs-based binary compounds, which were used as flame retardants. [ABSTRACT FROM AUTHOR]

• An ionic confinement engineering approach is proposed to facilitate dynamic ionic crosslinking. • The ionomers deliver low dielectric-k property, high stretchability and fast self-healing capability. • The EGaIn-infused stretchable device is designed for electronic device reconfiguration. Ionomers are gaining much attention in the fields of soft robots, flexible electronics, and artificial intelligence. However, intrinsic dynamics modulation of ionomer molecules to achieve desirable properties is highly required and challenging due to a lack of understanding of the interactions between polymerics and ionic species. In this study, a novel ionic confinement engineering approach was employed, in which the composition of a copolymer, namely, PTAE-Fe, was adjusted to facilitate dynamic ionic crosslinking, which enables high stretchability (>10000 % elongation). The proportion of ionic functional groups in PTAE-Fe significantly enhanced the self-healing efficiency up to 95 %. The ionic confinement strategy also promotes electron momentum locking, resulting in a low dielectric-k property (D k < 2.5), while a reduction in the heat release rate of 69.1 % makes the ionomer an excellent flame retardant material. In addition, a eutectic gallium-indium (EGaIn)-infused stretchable device and low D k flexible ink were designed according to the ionic confinement strategy. The as-fabricated ionomer is expected to benefit a wide range of energy and storage technologies. [ABSTRACT FROM AUTHOR]

[Display omitted] • Phthalocyanine-zirconium polyphosphazene functionalized BP was obtained by crosslinking reaction. • BP-ZrPZN effectively reduced the total smoke release decreased by an impressive 62.7 %. • BP-ZrPZN can comprehensively improve the fire safety and mechanical properties of EP. The existence of lone pair electrons on the surface of black phosphorus (BP) is a good electron acceptor, which has good structural stability when it forms new electron donor-electron acceptor pairs when combined with electron donators such as phthalocyanine. In order to bond functional groups available for reaction on the surface of BP, the lamellae group density was increased by functionalizing BP with benzoic acid diazonium salt, and then the carboxylated BP was covalently grafted with phthalocyanine zirconium, and finally the phthalocyanine-zirconium polyphosphazene functionalized BP (BP-ZrPZN) was obtained by crosslinking reaction. Subsequently, BP-ZrPZN was added into the EP matrix as nano filler to form the reinforced system. The results showed that the thermal stability and fire safety of EP composites containing 2 wt% BP-ZrPZN were significantly improved. The peak heat release rate and total heat release rate were reduced by 56.8 % and 54.1 %, respectively, and the limited oxygen index was up to 33 % and UL94 value was V-0. In addition, the presence of BP-ZrPZN greatly improved the ability of BP to inhibit toxic smoke. The total smoke yield of EP composites decreased by 62.7 %. The tensile strength and impact strength increased by 36.1 % and 50.6 % respectively. Therefore, the functional strategy of phthalocyanine in this work will provide a reasonable and feasible way to optimize the flame retardancy and smoke suppression effect of BP. [ABSTRACT FROM AUTHOR]

The essence of this work lies in the large-scale production of high-quality graphene sheets and simultaneous functionalization with new electrochemical route. A multifunctional flame retardant with phosphazene rings is well designed to simultaneously exfoliate and functionalize graphene. Due to the antioxidant function of flame retardant, the electrochemically-exfoliated graphene sheets exhibit high quality and low defect (C/O = 10.4). Furthermore, the obtained graphene is noncovalently modified to form flame retardant functionalized graphene sheets (FGNS). Subsequently, the FGNS is applied to improve fire safety and mechanical performance of thermoplastic polyurethane (TPU). Compared to pure sample, the peak heat release rate and total heat release of TPU composites with the addition of 4 wt% FGNS are significantly decreased by 46.3% and 20.2%, respectively. The elongation at break and tensile strength of TPU are enhanced by 11.6% and 59.9%, respectively, with the addition of 2.0 wt% FGNS. The significant enhancement in fire safety is due to conjunct effects of FGNS and the flame retardant. Lower defect of graphene provides more stable layer structure, thus FGNS plays a remarkable barrier action to confine the escape of degradation products. The coated flame retardant is conducive to form compact and robust char residue by reacting with degradation products. In addition, the flame retardant facilitates the load transfer to the robust graphene sheets with improved interface interaction. Through an electrochemical route, designing a multifunctional flame retardant to simultaneously exfoliate and modify graphene provides new possibility for the industrialized application of graphene. [ABSTRACT FROM AUTHOR]

As one of the most widely used polymers, the intrinsic brittleness and high flammability bring about a stringent requirement for the practical application of epoxy resins (EPs). It is difficult to toughen EP without compromising its mechanical and thermal properties for many conventional toughening agents. Here, a novel furan-derived bio-based polyphosphazene (PFMP) with a flexible backbone and rigid side groups was prepared by the nucleophilic substitution reaction between polydichlorophosphazene (PDCP) and furfuralcohol. The resultant PFMP was incorporated into EP to realize exceptional toughening, strengthening, and flame retardant function. By adding 15% of PFMP, the limit oxygen index value is from 25% (EP) to 33% (EP/PFMP-15) and reaches the UL-94 V-0 rating. According to the cone calorimeter results, EP/PFMP-15 exhibits exceedingly reduced peak heat release rate (pHRR) (50.2%) and total heat release (THR) (49.6%). The significantly increased fire performance index (FPI) and decreased fire growth rate index (FIGRA) of EP/PFMP-15 demonstrate an improvement in its flame retardancy. The catalytic carbonization effect (condensed phase) and radical quenching effect (gas phase) of PFMP account for the greatly improved flame retardancy. Moreover, the impact and tensile tests indicate that PFMP can ameliorate the mechanical performance of EP with a maximum increase of impact strength (111.8%) and elongation at break (35.2%) for EP/PFMP-5. With 15% PFMP added, the tensile strength of EP/PFMP-15 increases by 40.4%. This work demonstrates that PFMP is expected to overcome shortcomings (flammability, toughness, and strength) of EP and spread its applied fields. [Display omitted] • Bio-based polyphosphazene with furfuralcohol side groups (PFMP) was synthesized. • PFMP exhibits evident flame retardant and mechanical enhancement effect on epoxy resins (EP). • The peak heat release rate of EP/PFMP-15 was 50.2% lower than pure EP. • The impact strength of EP/PFMP-5 was 111.8% higher than pure EP. [ABSTRACT FROM AUTHOR]

[Display omitted] • A new flame retardant DOPONH 2 -S was synthesized. • It solved the problems of epoxy resin (EP) including flammability and brittleness. • DOPONH 2 -S achieved high efficiency in reducing THR, P -HRR and EHC of EP. • DOPONH 2 -S increased the impact strength and thermal stability of EP. Epoxy resin (EP) has two shortcomings: flammability and brittleness. Previous studies have improved brittleness or flame retardancy but they will compromise the glass transition temperature (T g) and thermal stability. Herein, a novel DOPO based phosphorus-, nitrogen- and sulfur-co-contained macromolecular flame retardant (DOPONH 2 -S) was synthesized and incorporated into EP to improve its flame retardancy and toughness with not damaging T g and thermal stability. After curing, both T g and the tensile strength of EP-2 improved at the addition of DOPONH 2 -S is 6.75 wt%. Simultaneously, the thermogravimetric analysis (TGA) results showed DOPONH 2 -S is helpful increasing the thermal stability of EP composites and protecting the polymer from further decomposition. In the fire safety test, EP-2 achieved V-0 rating in the vertical burning test and obtained a limiting oxygen index value of 30.5%. In comparison with pure EP, the peak heat release rate, total heat release and effective heat of combustion of EP-4 incorporated with 10.0 wt% DOPONH 2 -S were reduced by 59.1%, 58.5% and 46.3%, respectively. A two-phase mechanism was discussed to explain the combination effect in DOPONH 2 -S. In condensed-phase, rich char residue prevents the exchange of mass and heat during combustion. It also obstructs the release of combustible gases into the combustion zone. In gas-phase, the produced phosphorus- and sulfur-containing free radicals can capture active free radicals (H· and OH·), thus ending the chain reaction of combustion. Moreover, the addition of DOPONH 2 -S apparently improved the impact strength (62.5%). This work provided ideas for the development of multifunctional EP. [ABSTRACT FROM AUTHOR]

The dispersion problems of black phosphorus (BP) in polymer-based composites can be solved by designing isolation structure. An isolating structural material with functionalized BP nanosheets and polystyrene (PS) microspheres was prepared by molding method. Firstly, the sulfonated BP nanosheets with negative charge were obtained by electrochemical diazo modification (electrochemical diazo modification of BP is first report, and achieved good synchronous stripping and modification effect). The sulfonated BP and the PS microspheres with positive charge were self-assembled to form composite microspheres through strong electrostatic interaction. The prepared composite microspheres were further hot pressed near the glass transition temperature to selectively distribute the BP nanosheets at the interface of the fused PS microspheres. Therefore, the PS-BP isolation structure with uniform dispersion and reasonable distribution was obtained in the PS matrix. Thanks to this unique structure, the maximum heat release rate and smoke production rate reduction of the isolation structure can reach 50.1% and 43.3%, which at an excellent level in the same kind of two-dimensional material based composites. The tensile strength is maximally increased by 71.7% when the filling amount is 1.0 wt%. This simple method provides a new strategy for modifying BP and is expected to be applied to the preparation of high performance polymer-based composites. [Display omitted] • An isolation structure with black phosphorus and polystyrene microspheres is achieved. • The electrochemical diazo modification of black phosphorus is the first report. • The heat release rate and smoke production rate of the isolation structure is significantly reduced. [ABSTRACT FROM AUTHOR]

[Display omitted] • The octopus sucker-inspired M@CN with hierarchical structure is successfully synthesized. • The Interface engineering between M@CN and TPU matrix is greatly improved. • TPU/M@CN demonstrates superior improvement of TS of 79.5% and EB of 113.5%. • The pHRR and smoke suppression of TPU/M@CN-3 are reduced by 54.1% and 40.4%, respectively. Developing high-performance polymer materials with excellent mechanical properties and fire safety in fires remains a thorny challenge. In this article, hierarchical structure MXene@carbon nanotubes (M@CN) are prepared through electrostatic interactions for enhancing the interfacial engineering of thermoplastic polyurethane (TPU). With biomimetic method, the TPU/M@CN-3 nanocomposites performed octopus sucker-inspired structure during the stretching behavior, making the tensile strength and elongation at break of TPU/M@CN-3 increase 79.5% and 113.5%, respectively. What's more, thanks to the 1D-2D hierarchical structure of M@CN, fire safety of these TPU nanocomposites were extremely reinforced. Compared with the pure TPU, the TPU/M@CN-3 of peak heat release rate (pHRR) and smoke density max (Ds max) reduced by 54.1% and 40.4%. The production rates of carbon monoxide (CO) and carbon dioxide (CO 2) were reduced by 62.7% and 33.0%, respectively. Therefore, this work provides a convenient way to prepare a high-performance TPU with highly mechanical properties and fire safety through enhacing the interfacial engineering. [ABSTRACT FROM AUTHOR]

[Display omitted] • Utilizing the flame retardancy advantages of polyphosphazene and melamine, PPM was firstly designed and synthesized. • PPM has a positive effect on enhancing the fire safety and mechanical properties of BMI. • PPM is an integrated intumescent flame retardant and the cooperation effect of polyphosphazene and melamine in PPM is revealed. In view of the problems of poor toughness and high fire risk of bismaleimide (BMI), a novel maleimide-functionalized triazine-rich polyphosphazene microsphere (PPM) was designed and prepared in this work by combining the flame retardant advantages of polyphosphazene and melamine. The functionalization of organic maleimide in PPM can improve the interfacial compatibility between PPM and BMI. With addition of 2.0 wt% PPM, the peak value of heat release rate (PHRR) and total smoke production (TSP) of BMI/PPM-2.0 decrease by 52.8 % and 30.8 %, respectively, while its impact strength increases by 97.5 %, which means that the fire safety and toughness of BMI/PPM are much better. The study on flame retardant mechanism of PPM reveals that PPM has obvious condensed-phase intumescent flame-retardant effect, which may be due to the similar composition of PPM and intumescent flame retardant. In addition, PPM has the phosphorus-oxygen radical flame-retardant effect in gas phase and also has the toughening effect of inorganic rigid particles on BMI performance. [ABSTRACT FROM AUTHOR]

• Cardanol-derived anhydride cross-linked epoxy thermosets achieved UL-94 V-0 grade. • A remarkable reduction in the PHRR value of 47.7% was observed. • Cardanol-derived anhydride imparted excellent toughness to the cured epoxy. • Cardanol-derived anhydride cross-linked epoxy showed high shape recovery efficiency of more than 96% With the increasing awareness of environmental protection, the development of high-performance bio-based epoxy resins has attracted more and more attention to reduce the dependence on the petroleum-based 4,4′-diaminodiphenylmethane (DDM). In this work, we synthesized two kinds of cardanol-based curing agents (Car-DCP-MAH and Car-DPC-MAH) as alternatives for petroleum-based DDM. The chemical structures of Car-DCP-MAH and Car-DPC-MAH were confirmed by 1H and 31P NMR. Compared with the traditional DGEBA/DDM thermoset, the cured DGEBA/Car-DCP-MAH and DGEBA/Car-DPC-MAH thermosets both displayed good intrinsic fire resistance in terms of higher LOI values (29% and 28%, respectively, versus 24.5%) and V-0 rating in the UL-94 test. Furthermore, the results of the cone calorimeter test showed a significant reduction in the peak heat release rate (PHRR) values of the cured DGEBA/Car-DCP-MAH and DGEBA/Car-DPC-MAH which were 42.3% and 47.7%. The flame retardancy of these two systems was mainly due to the great carbonization ability and the formation of the intact and compact char layer. Owning to the flexible long alkyl chain in the crosslinking network, the toughness of the cured DGEBA/Car-DCP-MAH and DGEBA/Car-DPC-MAH products was greatly improved with the higher elongation at break and impact strength. Additionally, the cured DGEBA/Car-DCP-MAH and DGEBA/Car-DPC-MAH thermosets both showed preferable shape memory properties with a high shape recovery efficiency of 98.6% and 96.3%. This study provides a novel strategy to achieve bio-based epoxy thermosets with intrinsic anti-flammability, toughness and shape memory effect. [ABSTRACT FROM AUTHOR]

[Display omitted] • Photothermal of EP/SL-EBP-CoP is linearly increased (r2 > 0.994). • EP/SL-EBP-CoP 2 separately reduces PHRR, THR and PCOP by 59.88%, 39.26% and 36.41%. • Phosphorus, P-O-P and P-O-C are nodes, units and capture bonds in 3D sutured char. • Rupture molecules of char layer (C n H 2n+2 PO 4 , m / z = 168, 139 and 124) are discovered. To overcome the high flammability of polymers and endow them with photothermal capability, we fabricate the targeted nanofiller black phosphorus (BP) based SL-EBP-CoP for epoxy. Interestingly, the good ability of photothermal for EP/SL-EBP-CoP 2.0 nanocomposite changes with irradiation power can be linearly quantified (r2 > 0.94). Secondly, EP/SL-EBP-CoP 2.0 separately reduces peak heat release rate (HRR), total HRR and peak carbon monoxide (CO) production by 59.88%, 39.26% and 36.41% compared with EP, along with the lowest fire growth index. The significantly reduced hazard of heat and CO is attributed to the combined effects of 2D BP, catalysis of CoP and the structure of sutured char. Finally, the pyrolysis of BP-based flame retardants produces P 4 , P 3 and P 2 with an abundance of 77.10%, 6.75% and 14.70%. Moreover, flame retardant composites are highly dependent on the final char. This work demonstrates that phosphorus and P-O-P (PO x) are nodes and bonding units in the char, PO x bonds to the hydrocarbon fragments through P-O-C bonds. Particularly, pyrolysis molecules of suture and rupture of char (C n H 2n+2 PO 4 , m / z = 168, 139 and 124) are first discovered. This work booms the path and lays the foundations for the photothermal and fire safety of BP nanocomposites. [ABSTRACT FROM AUTHOR]

[Display omitted] • The polyaniline (PANI) is deposited on the surface of two-dimensional Ti 3 C 2 to obtain the Ti 3 C 2 @PANI hybrid for constructing waterborne polyurethane (WPU) composite. • Due to the existence of conductive fillers and the isolated structure, the electromagnetic shielding effectiveness of Q-FBP-WPU/Ti 3 C 2 @PANI composite is still higher than 20 dB after hundreds of stretching and bending. • The cone test results show that the peak heat release rate of Q-FBP-WPU/Ti 3 C 2 @PANI is decreased by 46.2%. To solve the increasing serious electromagnetic radiation pollution and limitations of metal-based electromagnetic shielding materials in flexible devices, the polyaniline (PANI) is deposited on the surface of two-dimensional Ti 3 C 2 to obtain the Ti 3 C 2 @PANI hybrid for constructing waterborne polyurethane (WPU) composite. Meanwhile, to address the flame risk of WPU composite, the two-dimensional black phosphorous (BP) is incorporated as a flame retardant to prepare isolated flame-retardant black phosphorous-waterborne polyurethane/Ti 3 C 2 @polyaniline(Q-FBP-WPU/Ti 3 C 2 @PANI) composite with isolated structure. Due to the existence of conductive fillers and the isolated structure, the Q-FBP-WPU/Ti 3 C 2 @PANI composite exhibited the highest electrical conductivity (2.23 S/m) and the electromagnetic shielding effectiveness (EMI SE) of 27.3 dB in the frequency range of 8.2–12.4 GHz (X-band) and retains higher than 20 dB after hundreds of stretching and bending, which completely satisfies the commercial demands. Compared with the composite with a disordered structure, the thermal conductivity of Q-FBP-WPU/Ti 3 C 2 @PANI is increased by 93.3%. The cone test results show that the peak heat release rate, total heat release, total smoke production and total CO production of Q-FBP-WPU/Ti 3 C 2 @PANI is decreased by 46.2%, 16.3%, 21.2% and 15.5% than that of pure WPU, certifying the fire safety of WPU are greatly improved. This work supports a novel and applicable idea for constructing functional electromagnetic shielding materials. [ABSTRACT FROM AUTHOR]

• Microwave assisted grafting of AA onto the PA6.6 fabric surfaces was done. • Layer by layer deposition and HP cross-linking were followed. • A maximum reduction in pHRR by ca. 50% was achieved. • Super-hydrophilic surfaces were obtained. • Such coating could retain anti-dripping properties even after 10 launderings. Microwave-assisted surface modification of polyamide 6.6 (PA6.6) fabrics was carried out in a grafting polymerization technique in the presence of acrylic acid (AA) monomer with an aim to enhance the extent of surface functional groups onto the PA6.6 fabric surfaces. In the next step, the surface modified fabric substrate was gone through a layer by layer (LbL) deposition process in the presence of some hybrid (organic/inorganic) polyelectrolytes in imparting hydrophylic and flame retardant properties and finally, the as prepared coating was subjected to a cross-linking treatment aided by hypo-phosphorus acid (HP) in enhancing the stability of the same. From the obtained results, it was revealed that the simultaneous microwave assisted grafting, LbL deposition and HP cross-linking left positive impacts in improving the flame retardant performance and hydrophilicity of PA6.6 fabrics along with the enhancement of coating stability in laundering. For example, acrylic acid grafted PA6.6 fabric sample with a 5-BL deposition and cross-linked with HP (i.e., PA6.6-g-AA-5BL-HP) attained a limiting oxygen index (LOI) value up to 23.5%, while exhibiting a significant level of reduction in the peak heat release rate (pHRR) by ca. 50 %. In line, a super-hydrophilic surface was obtained for this fabric sample as the water contact angle value declined to 0º. Furthermore, such kind of surface modification displayed a considerable level of coating stability during laundering as the anti-dripping properties still exist even after 10 home launderings. [Display omitted] [ABSTRACT FROM AUTHOR]

A fully bio-based epoxy thermosetting network was prepared by curing a renewable luteolin-derived epoxy resin (DGELU) with a furan-derived hardener, 5, 5′-methylenedifurfurylamine (DFA). For comparison, a control sample was prepared by curing the petroleum-based commercial epoxy diglycidyl ether of bisphenol A (DGEBA) with a petroleum-based hardener, 4, 4′-diaminodiphenylmethane (DDM). The glass transition temperature (T g) was found to be 216 °C for the cured DGELU/DFA, which was 67 °C higher than that of the cured DGEBA/DDM. The storage modulus at 30 °C and the tensile strength of the cured DGELU/DFA were 82.5 % and 23.2 % higher than those of the cured DGEBA/DDM. The benzopyrone unit of the luteolin structure was conducive to exceptional charring, and the char yield for thermal decomposition in the nitrogen of the cured DGELU/DFA was 3.2-fold higher than that for the cured DGEBA/DDM. As expected, the cured DGELU/DFA displays a relatively high limiting oxygen index (LOI) of 38.0 % and a UL-94 V-0 classification, whereas the petroleum-based counterpart exhibited a much lower LOI of 24.0 % and no classification in the UL-94 test. An in-vitro cytotoxicity study indicated that the cured DGELU/DFA showed no cytotoxic effect against normal fibroblast cells after 24 and 72 h. Because of these fascinating features, the DGELU/DFA thermosetting network was deposited onto wood surfaces for evaluation as a flame-retardant coating. Compared with the wood treated using the cured DGEBA/DDM coating, wood coated with the cured DGELU/DFA showed a super fire-safe property that could lead to a 55.8 %, 12.4 %, and 11.5 % decrease in peak heat release rate (PHRR), total heat release (THR), and total smoke production (TSP), respectively. An anti-flammable, high strength and non-toxic bio-derived epoxy thermosetting network for highly safe epoxy coating applications has been developed. • A fully bio-based epoxy thermoset (DGELU/DFA) has been prepared from luteolin. • DGELU/DFA showed higher Tg and tensile strength than its petroleum-based counterpart. • DGELU/DFA displayed anti-flammability with a high LOI of 38.0 % and a UL-94 V-0 grade. • DGELU/DFA showed no cytotoxic effect against normal fibroblast cells. • DGELU/DFA is suitable as a flame-retardant and eco-friendly coating for wood. [ABSTRACT FROM AUTHOR]

Polyester fabric is ubiquitously applied for clothing, furniture and transportation, whereas its flammability with severe dripping often causes secondary hazards. Herein, it is highly imperative to impart excellent flame retardant to polyester fabric. In this work, a coating for polyester fabrics was prepared through a continuous dipping and ultraviolet (UV) curing process, which exhibited high-efficiency flame-retardant, anti-dripping and washing resistance. Firstly, the surface of polyester fabric was pretreated with plasma for providing more grafting sites of polyester fabric. Then, the flame retardant 6-((((2-(acryloyloxy) ethoxy) (oxo)(phenyl)phosphonio) oxy) methyl) dibenzo[c,e][1,2]oxaphosphinine 6-oxide (DPEA) and Tri(acryloyloxyethyl) phosphate (TAEP) were successfully synthesized and applied to the coating by UV-curing. In vertical burn test, the damage length of polyester with DPEA and TAEP (PET-D 3 /T 4.5) was reduced from 300 mm of pristine PET to 100 mm with no dripping. In the Thermogravimetric Analysis (TGA) test, the char residue of PET-D 3 /T 4.5 in nitrogen increased to 26.7 % compared with 9.7 % of pristine polyester. More specifically, the Peak Heat Release Rate (PHRR) and Total Heat Rate (THR) of PET-D 3 /T 4.5 decreased 43.3 % and 22.2 % in the Micro-scale Combustion Calorimetry (MCC) test, which reflected excellent thermal stability and flame retardant properties. In addition, the Limiting Oxygen Index (LOI) of PET-D 3 /T 4.5 only dripped from 24 % to 23.5 % after ten standard laundering cycles, indicating prominent water resistance. Remarkably, Thermogravimetric Analysis-Fourier transform infrared (TG-IR), Scanning Electron Microscope (SEM) and X-ray Photoelectron Spectroscopy (XPS) have been performed for investigating the mechanism of flame retardant. Thus, a strategy with convenience and economics is proposed, which is of gargantuan significance to the improvement of coating durability through plasma surface treatment and UV-curing. [Display omitted] • The improvement of coating durability through plasma surface treatment and UV-curing. • The damage length of coated polyester is reduced to 100 mm with no dripping. • The peak heat release rate and total heat rate of coated polyester is decreased by 43.3 % and 22.2 %. • The flame-retardant mechanism of different valence phosphorus in coating is studied. • A simple coating strategy for giving versatility to polyester fabric. [ABSTRACT FROM AUTHOR]

• A vanillin-derived cyclotriphosphazene-cored triazole compound (HHCTP) was synthesized. • The HHCTP-modified epoxy achieved a UL-94 V-0 classification and an LOI of 31.5%. • The addition of HHCTP preserved the thermo-mechanical properties of epoxy resins. A vanillin-derived cyclotriphosphazene-cored triazole compound (HHCTP) was successfully synthesized as a flame retardant for epoxy thermosets with high efficiency while preserving their thermomechanical properties. 1H- and 31P nuclear magnetic resonance (NMR), as well as Fourier Transform infrared (FT-IR), were applied to confirm the molecular structure of HHCTP. The dynamic mechanical analysis (DMA) measurements demonstrated that the introduction of HHCTP improved the storage modulus of the epoxy composites but decreased the glass transition temperature. The epoxy thermoset containing 7.5 wt% HHCTP (EP/HHCTP-7.5) achieved a UL-94 V-0 classification and an LOI of 31.5%, manifesting its outstanding flame-retardant efficiency. In addition, the cone calorimeter results showed that the total heat release (THR) and the peak value of the heat release rate (PHRR) of EP/HHCTP-7.5 were decreased by 35.6% and 50.0%, respectively, in comparison with those of the unmodified epoxy. To further study the flame retardant mechanism of HHCTP, pyrolytic gas species were detected utilizing thermogravimetric-infrared spectroscopy (TG-FTIR). In addition, the microstructure of the char residues was analyzed via X-ray photoelectron spectroscopy (XPS) and scanning electron microscope (SEM) techniques. The phosphazene groups in HHTCP clearly stimulated the production of an intumescent, compact, and strong char layer, which improved the flame retardancy of the DGEBA matrix during burning, according to the SEM data. As a result, the underlying components were protected from further degradation and combustion, resulting in effective flame retardancy of the DGEBA thermoset. [ABSTRACT FROM AUTHOR]

Devoting to coping with safety risk spreading with polymers, this work achieves dramatic synergistic improvements in composite toughness, photothermal healing, and fire safety through a novel targeted modification strategy for black phosphorus (BP). In detail, we herein use the emerging 2D BP as a template for in-situ growth by covalent triazine framework (HBP-CTF). Incorporating gradient increased HBP-CTF (1, 2, 4 wt%) into polystyrene (PS), the elongation at break increased by 61.59%, 74.60% and 62.82% for composites, respectively. This is attributed to the synergistic effects of two components of HBP-CTF as stress conduction unit and interface and dispersion improver, respectively. Furthermore, PS/HBP-CTF composites achieve photothermal healing over 96% in strength and elongation at break induced by outstanding photothermal properties (linearly quantifiable, R2 > 0.997). Noted, PS/HBP-CTF 2.0 and PS/HBP-CTF 4.0 achieve record reductions of 61.77% and 69.85% in peak heat release rate, accompanied by dramatically reduced total heat release. Taking the pyrolysis of HBP-CTF as an index, this work proposes the idea of using P 4 as the key product to monitor and distribute gas phase effects for BP-based flame retardants. The hybridization of CTF to HBP promotes the slow and continuous release of P 4 in the gas phase, revealing the structure and composition of char that cross-linking P and N. This work provides strategies for synergistically overcoming composite brittleness, crack failure, and high flammability, paving the way for practical applications. [ABSTRACT FROM AUTHOR]

Taking into consideration the frigid and thunderstorms, the flame retardancy and de-icing performance are simultaneously desiderated for some open-air key equipment, such as air fuselage and wind turbine blades. Here, inspired by the anti-reflection phenomenon of moth eyes and cicada wings, a multi-functionalized and biomimetic MXene@SnO 2 hierarchical nanostructure is prepared to effectively impart flame retardancy and solar de-icing performance to thermoplastic polyurethane (TPU) resin used widely as the finishing coat of protective materials of open-air equipment. Based on the catalytic effect and barrier function, the addition of hierarchical MXene@SnO 2 nanostructures also effectively decreases the release of heat and toxic smoke from PU resin, as confirmed by reductions of 50.5% and 33.1% in the peak heat release rate and smoke production rate, respectively. Due to the appropriate refractive index, the light reflection phenomenon is effectively suppressed, thus promoting solar absorption (∼90% at 0.4 mm film) and photo-thermal conversion (∼74.2 °C with simulated solar illumination of 1.0 kW/m2) in TPU-MXene@SnO 2 nanocomposites. Within the environment of −20 °C, the surface temperature of TPU-MXene@SnO 2 nanocomposites is still up to 32.7 °C and the surface ice pellet begins to melt at ∼40s, much earlier than 600s of pure TPU resin. In addition, the practical application of functionalized TPU nanocomposites is further improved by the higher mechanical properties, attributed to the strong interfacial interaction. Inspired by moth eyes and cicada wings, flame retardancy and solar de-icing performance are first integrated into polymer materials, thus effectively promoting their application in some extreme environments. [Display omitted] [ABSTRACT FROM AUTHOR]

• A novel cactus-like structure of BP@MoS 2 hybrids was designed and synthesized. • The tensile strength and fracture strength of WPU/BP@MoS 2 -2.0 increase by 57.7% and 36.5%. • The PHRR and TSP of WPU/BP@MoS 2 -2.0 reduce by 50.3% and 52.0%. • BP and MoS 2 have a cooperative effect in suppressing the heat release behavior of WPU/BP@MoS 2. Design novel flame retardant and mechanical enhancing agents of waterborne polyurethane (WPU) is a crucial issue for expanding its application. Herein, BP@MoS 2 hybrids was designed and prepared to enhance the fire safety and mechanical properties of WPU and BP@MoS 2 possessed a novel cactus-like structure. BP@MoS 2 was prepared in a two-step method including preparation of black phosphorus (BP) sheets by chemical vapor transfer method and preparation of BP@MoS 2 by in situ growth of molybdenum disulfide (MoS 2). with adding 2.0wt% BP@MoS 2 , the tensile strength and fracture strength of WPU/BP@MoS 2 -2.0 increase by 57.7% and 36.5%, respectively. The peak value of heat release rate (PHRR) and total smoke production (TSP) of WPU/BP@MoS 2 -2.0 also reduce by 50.3% and 52.0%, which indicates that fire safety and mechanical performance of WPU/BP@MoS 2 -2.0 is effectively enhanced. Meanwhile, BP@MoS 2 has both condensed phase and gas phase flame retardant effect on WPU. In condensed phase, the residue char of WPU/BP@MoS 2 is with excellent physical barrier effect. In gas phase, BP@MoS 2 can inhibit the generation of flammable volatiles such as aromatic and aliphatic compounds during burning of WPU/BP@MoS 2 , thereby inhibiting the heat release and smoke release behavior of WPU/BP@MoS 2. [Display omitted] [ABSTRACT FROM AUTHOR]

Towards simultaneously improving the moist ambient stability and flame retardancy efficiency of black phosphorus (BP) nanosheets, cross-linked polydimethylsiloxane (PDMS) is simultaneously synthesized and grafted onto the surface of BP nanosheets, thus obtaining hydrophobicity to shield the water molecule and synergistic flame retardant effect. Compared to badly damaged morphology of pure BP nanosheets, the well-ordered crystal structure confirms that PDMS-BP nanosheets are moist-environmentally stable. With the grafting of PDMS, BP nanosheets present higher flame retardancy efficiency to thermoplastic polyurethane (TPU). The reductions of 59.6% and 14.3% are presented in peak heat release rate (PHRR) and total heat release (THR) of TPU resin, compared with pure TPU. The CO 2 and CO produced by resin combustion are also decreased by 42.8% and 29.3%, indicating lower gas toxicity. Based on the morphology observation and element analysis of char residue, the synergistic effect between phosphorus and silicon elements is responsible for the flame retardancy improvement. Such a route simultaneously provides a valuable reference for moist-environmentally unstable nanomaterials and develops the practical application of BP nanosheets in polymer composites fields. [Display omitted] • Cross-linked PDMS bonds with BP nanosheets by noncovalent interaction. • Moist ambient stability is imparted to BP nanosheets. • Fire safety and water resistance of polymer are enhanced simultaneously. • Heat, smoke, and toxic CO during polymer combustion are greatly decreased. [ABSTRACT FROM AUTHOR]

[Display omitted] • Environmentally friendly new flame retardant f-HAPNW was successfully prepared. • f-HAPNW achieved high filler efficiency in reducing THR and TSP of UPR nanocomposites. • UPR/f-HAPNW 0.5 achieved an 61.2 % increase in impact strength. • Novel flame retardancy and mechanical reinforcement mechanism about f-HAPNW. Non-toxic, low-smoke, high-efficiency and environmentally friendly flame retardants have become a hot issue at present. Here, polyphosphazene crosslinked by hexachlorocyclotriphosphazene (HCCP), 3-aminopropyltriethoxysilane (APTES), and dopamine (DA) was used to modify hydroxyapatite nanowires (HAPNW), obtaining a new environmentally friendly nanohybrids (f-HAPNW). Immediately afterwards, f-HAPNW was incorporated in unsaturated polyester (UPR) matrix in the presence of a nanowire structure with a high aspect ratio, accompanied by excellent interfacial compatibility. The incorporation of a small amount of f-HAPNW achieved an overall improvement in the fire safety and mechanical properties of UPR nanocomposites, including 23% decrease in total heat release rate (THR), 25.7% and 29.5% reduction in total smoke production (TSP) and the peak of CO production rate (PCOP) when the content was 2.0 wt%; 80.1% and 11.9% simultaneous increase in tensile strength and fracture elongation, and 61.2% increase in impact strength when the content was 0.5 wt%. Compared with similar previous research, the introduction of bio-based materials and environmentally friendly flame retardants in the design achieved significant flame-retardant filler efficiency, while considering the issues of reducing smoke release and environmental pollution. In general, this work innovatively prepared an environmentally-friendly hierarchical f-HAPNW structure, and achieved a comprehensive improvement in the performance of UPR nanocomposites, providing a reference idea for the design of high-performance UPR nanocomposites. [ABSTRACT FROM AUTHOR]

A novel carbon fiber/MXene coalition (CF-Ar-MXene) is synthesized via a bidirectional aryl diazonium chemistry method using p-phenylenediamine as a chemical bridge, which effectively combines the two materials with different dimensions and makes full use of the advantages of both. CF-Ar-MXene coalition materials achieve high surface roughness and rich oxygen-containing active groups due to the presence of MXene on the surface of CF, which leads to the favorable interfacial interaction and compatibility between CF-Ar-MXene and epoxy resin (EP) matrix. As expected, after the incorporation of CF-Ar-MXene coalition into EP matrix, the flame retardancy and mechanical properties of EP composites are significantly improved. For example, with the addition of 3 wt% CF-Ar-MXene coalition, the peak heat release rate (PHRR), total heat release (THR) and total smoke production (TSP) of EP composites decrease by 42.6%, 48.2% and 32.1%, respectively. Meanwhile, the TG-IR results indicate that the amount of combustible volatile products and toxic gases also significantly decrease. Notably, with 2 wt% loading of CF-Ar-MXene coalition in EP composites, the tensile strength and elongation at break increase by 49.9% and 40.5%, respectively. Therefore, the efficient cooperation between CF and MXene in CF-Ar-MXene coalition and excellent interface compatibility with EP matrix are the main reasons for the excellent flame retardancy and mechanical properties of EP/CF-Ar-MXene composites. [Display omitted] • CF-Ar-MXene coalitions were prepared by a bidirectional aryl diazonium chemistry method for the first time. • The method used in this experiment is efficient and eco-friendly compared with the traditional modification method for CF. • CF-Ar-MXene coalitions achieved high filler efficiency in reducing the fire hazards and smoke production of EP. • Mechanical properties of EP/CF-Ar-MXene composites were efficiency enhanced. [ABSTRACT FROM AUTHOR]

To tailor the enhancement strategies for polymers according to structure, inspired by the concept of "Cannikin's Law", this work proposes and exemplifies a novel strategy for reinforcing the carbonate linkages to simultaneously improve the thermal and fire safety of polycarbonate (PC). Herein, we introduce MIL-53(Al) to functionalize black phosphorus (BP@MIL-53) via a simple method of hydrothermal. As expected, the incorporation of BP@MIL-53 (1.0 wt%) in PC, resulted in an increase in T 1% of 32 °C and 41 °C under nitrogen and air respectively, along with the reduction of 49.4% and 19.3% for peak heat release rate and total heat release. Moreover, PC/BP@MIL-53-1.0 passed the V-0 rating of UL-94 with a high limiting oxygen index (LOI) value of 30.5%, which achieved the dual purpose of simultaneously enhancing the thermal stability and flame retardancy of PC. In addition, the addition of flame retardants had no effect on the tensile strength of the PC. These results demonstrate the high flame retardant efficiency of BP@MIL-53 at ultra-low addition levels. Moreover, these results also illustrate the forward-looking nature of the strategy of tailoring flame retardants to the properties of the substrate. This work combines the advantages of black phosphorus (BP) and Mental organic frameworks (MOFs) materials. The carbonate linkages reinforcement approach provides a viable, new, and scalable idea for polyester compounds' thermal and fire safety properties. [Display omitted] • Novel flame retardants designed to suit the structure of polycarbonate. • Significantly improved thermal stability of polycarbonate. • Highly efficient flame retardant with ultra-low addition levels. • Ester-based reinforcement and char formation strategies inspired by the "Cannikin's Law". [ABSTRACT FROM AUTHOR]

The weak anti-oxidation and smoke-suppression abilities limit the use of black phosphorus (BP) in the preparation of high-performance flame-retardant epoxy resin (EP) composites. Here, aromatic diazonium chemistry was used to graft phenylboronic acid on the surface of few-layer BP nanosheets (BPNSs) to obtain passivated BP-based nanomaterials (BP-DPBA). Then, a novel multifunctional nano flame retardant BP-DPBA@Co-BO was obtained by anchoring amorphous cobalt-based borate (Co-BO) on the surface of BP-DPBA through a low-temperature reduction reaction. Subsequently, BP-DPBA@Co-BO was incorporated into EP matrix in the form of nanofillers and formed a mechanically enhanced system. As expected, EP nanocomposites containing 2 wt% BP-DPBA@Co-BO achieves greatly improvements in thermal stability and fire safety, with 93% increase in char yield (CY) during pyrolysis, 48.4% and 41.7% decrease in peak heat release rate (PHRR) and total heat release (THR) during combustion respectively, a limiting oxygen index (LOI) value up to 32.5% and a UL94 rating of V0. In addition, the presence of Co-BO greatly improves the ability of BP to suppress toxic smoke. Specifically, EP/BP-DPBA@Co-BO 2.0 achieves a 25.4% reduction in total smoke production (TSP) during combustion. In particular, the maximum 36.2% and 73.2% increases are achieved in storage modulus and impact strength, respectively, confirming that BP-DPBA@Co-BO can effectively enhance the mechanical properties of EP. Therefore, this work provides a feasible solution for loading high-valence metal compounds on the surface of BPNSs, and prepared high-performance EP nanocomposites with enhanced fire safety and mechanical properties. [Display omitted] [ABSTRACT FROM AUTHOR]

[Display omitted] • BP-Ti 3 C 2 nanohybrids were obtained by two-electrode electrochemical exfoliation method. • The smoke release of WPU/BP nanocomposites during combustion was suppressed with the introduction of Ti 3 C 2. • The mechanical properties and fire safety of WPU were simultaneously improved. The low exfoliation yield and large solvents consumption have become the major issue that limits the commercial application of two-dimensional nanomaterials. Emerging as an effective and environmentally friendly approach, electrochemical exfoliation has been attached by extensive concern. Hence, a simple and environmentally friendly two-electrode electrochemical exfoliation method was put forward to prepare black phosphorus-MXene (BP-Ti 3 C 2) nanohybrids without consumption of any organic solvents. The integration of BP and Ti 3 C 2 also imparts higher fire safety and mechanical properties to waterborne polyurethane (WPU). With the incorporation of 2.0 wt% BP-Ti 3 C 2 , the peak heat release rate, total heat release, total smoke production and total CO 2 yield of WPU were decreased by 42.2%, 12.9%, 12.6% and 16.5%, respectively, exhibiting a great flame retardancy effect. The employment of electrochemical exfoliation method towards BP and Ti 3 C 2 nanosheets not only imparts higher fire safety to polymer composites, but also provides a referable environmentally friendly preparation for two-dimensional nanomaterials. [ABSTRACT FROM AUTHOR]

[Display omitted] • A novel phosphine oxide-containing hyperbranched polyol was synthesized. • RPUF containing POCHP and EG exhibit excellent fire safety and physical properties. • The production of CO and NO x during combustion of RPUF are significantly decreased by combination of POCHP and EG. In this work, a novel phosphine oxide-containing hyperbranched polyol (POCHP) was synthesized. Then POCHP and/or expandable graphite (EG) were incorporated into rigid polyurethane foam (RPUF). EG increases foam density and deteriorates compressive strength and thermal conductivity, but POCHP has opposite effects. A 12.8% improvement of compressive strength and slightly decreased density and thermal conductivity are achieved by ERPUF50 containing POCHP and EG. And it reaches a limited oxygen index of 30.0% and UL-94 V-0 rating with immediate self-extinguishing behavior after removing flame. The peak heat release rate, total heat release and total smoke production of ERPUF50 are reduced by 71.1%, 52.2% and 71.1% respectively via bi-phase flame retardant mechanisms. Interesting phenomena were observed that POCHP promotes the intumescence of EG after combustion. The results of combustion gas analysis reveal that single POCHP or EG reduces the production of CO but increases the generation of NO x. ERPUF50 exhibits a 52% decrement of CO and an unexpected 40% diminishment of NO x. ERPUF50 with excellent comprehensive properties can not only be used as fire safe thermal insulation material with high physical performances, but also significantly reduce the release of contaminative smoke, CO and NO x in fires and waste RPUF disposal by combustion. [ABSTRACT FROM AUTHOR]

As known, the poor toughness and low fire safety of bismaleimide resin (BMI) has become a problem which restricts its further application in advanced high-performance field. Therefore, a novel allyl-functionalized linear polyphosphazene (PMAP) was designed and synthesized. With inclusion of 3wt% PMAP, the peak heat release rate (PHRR) and total smoke production (TSP) of BMI/PMAP-3 are reduced by 51.3% and 17.8%, respectively. And the residual char of BMI/PMAP increases significantly as well. Furthermore, the flame-retardant mechanism of BMI/PMAP is proposed. In condensed phase, PMAP can participate in the formation of residual char of BMI/PMAP and the char layer is with an excellent physical barrier effect by the existence of phosphorus oxygen and phosphorus nitrogen cross-linking substances. In gas phase, phosphorous oxygen free radical is also generated from PMAP, which can capture gas-phase chain free radicals and inhibit gas-phase combustion. Moreover, the impact strength of BMI/PMAP-3 increases by 85.3%, which indicates that the toughness of BMI/PMAP is effectively enhanced. The toughening mechanism of PMAP on BMI can be assigned to elastomer toughening. Therefore, with modification of PMAP, BMI/PMAP is indeed of better comprehensive performance, which is in line with expectation and provides inspiration for the simultaneous flame-retardant and toughening modification of BMI. [Display omitted] • Innovation: bifunctional allyl functionalized linear polyphosphazene was firstly synthesized. • High-efficiency: the PHRR and impact strength of BMI/PMAP-3 is reduced by 51.3% and increased by 85.3%. • Mechanism: the flame retardant and toughening mechanism is proposed. [ABSTRACT FROM AUTHOR]

• Hydrophobic hierarchical OH-BN@CuCoOx was innovatively prepared by the MOF-derived strategy. • OH-BN@CuCoOx achieved high filler efficiency in reducing THR and TSP of BMI. • BMI/OH-BN@CuCoOx 0.5 achieved an 80 % increase in impact strength. • BMI/OH-BN@CuCoOx 0.5 achieved a 49 °C increase in Tg. In this work, the MOF-derived strategy was used to generate copper-cobalt metal oxide (CuCoOx) in situ on the surface of hydroxylated boron nitride (HO-BN), and a new type of nano-hybrid (HO-BN@CuCoOx) was obtained. Then, HO-BN@CuCoOx was dispersed in the bismaleimide resin (BMI) matrix in the form of a layered structure, forming a strong interface interaction. The results of the cone calorimeter test exhibited that the fire hazard and toxic smoke release of BMI nanocomposites containing 2 wt% HO-BN@CuCoOx were effectively suppressed, such as a 37.2% reduction in total heat release rate (THR), a 38.5% reduction at peak heat release rate (PHRR), 24.3% decrease in total smoke production (TSP) and 62.2% decrease in peaks of carbon monoxide (CO) production rate. Compared with previous studies, higher filling efficiency was achieved. In addition, BMI/HO-BN@CuCoOx 0.5 achieved an 80% increase in impact strength, revealing excellent toughness. In particular, the glass transition temperature (Tg) of BMI/HO-BN@CuCoOx 0.5 reached 330 °C, an increase of 49 °C compared to the pure sample, which increased the potential for application in extreme environments. Therefore, the developed new BMI/HO-BN@CuCoOx nanocomposites expanded the application potential of BMI in the high-end field. [ABSTRACT FROM AUTHOR]

This work was intended to clarify if the dyeing treatment could modify the functional properties of white substrate as well as the surface finishing would alter the initial color of dyed textiles. Thus, in this work, a kind of surface coating was applied to modify the flame retardant and hydrophilic properties of both the undyed (white) and dyed polyamide 6.6 (PA6.6) textiles using some novel compounds like chitosan (CS), montmorillonite (MMT), sodium alginate (ALG) and phytic acid (PA) in a quadralayer (QL) or a hexalayer (HL) fashion. The obtained results revealed that the dyed fabric samples exhibited better flame retardancy and hydrophilicity compared to the undyed one; indicating the dyeing treatment contributed in improving the functional properties. For example, the 5HL-deposited dyed fabric sample (i.e., PA6.6-D-5HL) showed a maximum reduction in the peak heat release rate (pHRR) by 32% and the 7.5QL-deposited dyed fabric sample (i.e., PA6.6-D-7.5QL) brought a water contact angle (WCA) value of 0°. However, this kind of surface finishing caused a slight loss in depth of color for the dyed fabric samples. [Display omitted] • A kind of surface coating was developed onto the undyed and dyed PA6.6 textiles. • Dyed fabrics showed better flame retardant properties compared to the undyed one. • Dyed fabric with a 5HL deposition obtained a maximum reduction in pHRR by 32%. • A super-hydrophilic surface was realized, especially for the dyed fabrics. • The applied finishing slightly altered the depth of color of dyed fabrics. [ABSTRACT FROM AUTHOR]

Conductive polymer composites have been caught increasing attentions in electromagnetic interference (EMI) shielding field. Due to the flammability of polymer and long-term high power working status, fire incidents on environment and human health must be taken into consideration during the preparation of the polymer materials. Thus, developing an EM waves-clean material with exceptional fire safety and smoke suppression capacity is the vital issue. In this article, a facile and eco-friendly approach to fabricate flame retardant polyurethane (PU) sponge was carried out by layer-by-layer (LBL) self-assembly with octaammonium-polyhedral oligomeric silsesquioxane (OAPOSS) and titanium carbide (Ti 3 C 2 T x) nanosheets. With the help of silicane and the barrier effect from Ti 3 C 2 T x , the peak heat release rate (pHRR) and total heat release (THR) decreased by 50%. Thanks to the exceeding catalytic capacity of Ti 3 C 2 T x nanoflakes, the production of harmful smokes or gases such as carbon oxide (CO) and carbon dioxide (CO 2) were sharply reduced with 71% and 27%, respectively. Furthermore, the flame retardant PU sponge obtained electromagnetic interference (EMI) shielding capacity after dip-coating procedure in MXene dispersion owing to the excellent electrical conductivity of Ti 3 C 2 T x nanosheets. The EMI shielding effectiveness (EMI SE) accomplished 32.57 dB and still remained 27.63 dB after 300 times compression. Therefore, this work could provide a promising way to accomplish flame retardant PU sponge with superior smoke suppression capacity, which could be used in cleaner production of modern electronics and EMI shielding materials. [Display omitted] • The facile cleaner approach to obtain multifunctional polyurethane (PU) sponge. • OAPOSS@MXene nanocoating was constructed on PU sponge via a clean layer-by-layer method. • The peak heat release rate and CO production was decreased by >50% and 71%, respectively. • Electromagnetic interference shielding capability remained >85% after 300 times compression. • Toxic fire effluents release-cleaner, electromagnetic waves-cleaner production of PU sponge were achieved. [ABSTRACT FROM AUTHOR]

[Display omitted] • 0D-2D hierarchical nanostructure was prepared via ZHS in-situ growing on Ti 3 C 2 T x. • EP-ZHS@M composites show up superior improvement of thermal conductivity of 328%. • EP-2.0 ZHS@M performed low pHRR of 54.91% and outstanding smoke suppression. • ZHS@M cut off the thermal disaster chain for safer package materials. Epoxy resin (EP) is widely used in the package of modern electronic products for thermal management, but the extremely flammability and toxicity release have restricted its further application. In this article, zinc hydroxystannate (ZHS) nanocubes were in-situ fabricated on the surface of titanium carbide (Ti 3 C 2 T x) MXene nanosheets (ZHS@M) for improving the thermal management capacity of EP. Due to the phonon thermal conductance from ZHS and electron-hole thermal conductance of Ti 3 C 2 T x , the thermal conductivity was improved by 328% compared with the neat EP, which was benefit to dissipate heat for reducing the possibility of thermal disaster chain happening. Furthermore, owing to the 0D-2D hierarchical structure of ZHS@M, the fire safety and smoke suppression of these EP composites were highly strengthened. The peak heat release rate (pHRR) and total heat release (THR) decreased by 54.91% and 58.74%, respectively. Moreover, hazardous gases of EP during the combustion were also efficiently reduced, and the generation of carbon oxide (CO) and carbon dioxide (CO 2) were decreased by 44.44% and 39.46% when the additive of ZHS@M was only 2 wt%. As a result, ternary catalytic effect and labyrinth structure improved the safety of EP in the thermal runaway incidents. Besides, EP-2.0 ZHS@M exhibited excellent tensile robustness (64.71 MPa) and modulus (2.39 GPa), which regarded as a reliable supporting material for electronics in thermal management field. Hence, this hierarchical EP-ZHS@M composites provided the help of cleaning the thermal accumulation and increasing fire safety while facing thermal runaway, which was significant to destroy the formation of thermal disaster chain and further applications of the modern electrons and devices. [ABSTRACT FROM AUTHOR]

• Hierarchical Ti 3 C 2 T X @PHbP-PHC architecture was innovatively synthesized. • Ti 3 C 2 T X @PHbP-PHC exhibited significant decrease in PHRR, THR and TSP. • BMI/Ti 3 C 2 T X @PHbP-PHC 0.5 achieved a significant increase in impact strength. • The synergistic mechanical reinforcement and flame-retardant mechanism among Ti 3 C 2 T X , PHbP and PHC was innovatively revealed. The effect of hindered amine light stabilizer on free radical quenching can be combined with the cross-linked polyphosphazene containing P N structure to improve the flame retardant efficiency of titanium carbide (Ti 3 C 2 T X) in both gas phase and condensed phase. Here, a hindered amine and polyphosphazene modified Ti 3 C 2 T X (Ti 3 C 2 T X @PHbP-PHC) was obtained. With the loading of Ti 3 C 2 T X @PHbP-PHC in the bismaleimide resin (BMI) increased to 2 wt%, an 43% reduction was achieved in the peak heat release rate (PHRR), and a 47% reduction in the total heat release rate (THR). Meanwhile, the total gaseous products and total smoke production (TSP) exhibited a similar decreasing trend. Furthermore, 0.5 wt% BMI system exhibited the highest storage modulus (2629 MPa) and impact strength (13.7 MPa), which were 21% and 76% higher than pure BMI, respectively. Therefore, the developed functionalized Ti 3 C 2 T X can be effectively used in BMI matrix, thereby providing reliable source material for the design of high-performance BMI resins that meet various application scenarios. [ABSTRACT FROM AUTHOR]

[Display omitted] • Few-layer black phosphorus was prepared via a simple hydrothermal Li+ intercalation method. • Aryl diazonium modified black phosphorus/ ultrafine yttrium oxide promisingly reduced the fire hazard of epoxy resins. • The possible mechanism of radical removal and catalytic carbonation was put forward. • This work might have a promising prospect for developing efficient covalent functionalized BP nanocomposites. Black phosphorus (BP), as a promising star of two-dimensional (2D) van der Waals family, has attracted extensive attention for its characteristic dimension effects, mechanical properties and thermal stability. Herein, we report a facile strategy of integrating aryl diazonium modified few Layer black phosphorus with loading of ultrafine yttrium oxide (BP-NH-Y), for reducing the fire hazard of epoxy resin (EP). The results of cone calorimetry test results manifest that the flame retardancy of EP can significantly improve by adding 2 wt% BP-NH-Y, for instance, the peak heat release rate (pHRR) and the total heat release (THR) is reduced by 47.0% and 48.1%, respectively. Especially, adding the BP-NH-Y nanosheets distinctly inhibite the diffusion of EP pyrolysis products (such as toxic CO, hydrocarbons etc.) during flaming. In particular, epoxy composites with only 1.0 wt% BP-NH-Y were able to achieve UL-94 V-0 rating with an oxygen index of more than 30. This work may have a promising prospect for developing efficient covalent functionalized BP nanosheets to meet the needs of sustainable applications. [ABSTRACT FROM AUTHOR]

[Display omitted] • The linear polyphosphazene and MoSe 2 hybrid (LPP-MoSe 2) was constructed. • EP/LPP-MoSe 2 exhibits low PHRR, THR, EHC, TSP, CO yield and CO 2 yield. • LPP-MoSe 2 shows synergistic flame retardant effect in gas-phase and condensed-phase. • LPP-MoSe 2 displays significant toughening and strengthening effect on EP. Epoxy resins (EP) are deemed as one kind of most commonly used thermosets, but immanently suffer from inflammability and brittleness. Herein, we report a newly designed hierarchical molybdenum diselenide (MoSe 2) nanotubes assembled from several-layered nanosheets, and then merged with linear polyphosphazene (LPP) for constructing LPP-MoSe 2 hybrids. LPP-MoSe 2 possesses great advantages in improving the properties of EP for their typical nanotube structure and the combination effect of transition metal, phosphorous and nitrogenous compounds. The developed EP/LPP-MoSe 2 composites present obvious reduction in flammability, obtaining a high LOI value of 29% and reaching V-0 rating in UL-94 test. They also exhibit obvious reduction in the heat hazards of EP, such as peak heat release rate (39.0%) and total heat release (24.8%), as well as the toxicity hazards including total smoke production (31.3%) and the yields of CO and CO 2. Gas-phase and condensed-phase mechanism are elucidated to explain the contribution of LPP-MoSe 2 to the fire retardation of EP. Moreover, the addition of LPP-MoSe 2 can also obviously enhance the mechanical properties of EP. The impact strength of EP is only 9 kJ/m2, while EP/LPP-MoSe 2 3.0 can reach up to 14.2 kJ/m2. Based on tensile test, the well-dispersed LPP-MoSe 2 also leads to significant elevation in tensile strength (74.6%) and elongation at break (100%) of EP. Our data demonstrate that LPP-MoSe 2 shows impressive performance in developing high-performance EP composites, thereby broadening the practical application of EP. [ABSTRACT FROM AUTHOR]

In order to enhance the fire resistance of poly(methyl methacrylate) (PMMA), a new transparent flame-retardant coating was prepared by coating hyperbranched poly(urethane-phosphine oxide) (HPUPO) onto PMMA surface, which was synthesized from 4,4′-diphenylmethane diisocyanate (MDI) and trihydroxymethylphosphine oxide (THPO). The ratio of MDI to THPO was changed to prepare HPUPO with different structures. The HPUPO coatings show a strong adhesion of 5B grade to PMMA and all coated PMMA have a high transparency as pure PMMA. In cone calorimetry test, peak heat release rate (PHRR) of all HPUPO coated PMMA decrease very obviously. The PHRR and total heat release (THR) values of PMMA-0.8 (HPUPO coated PMMA with the ratio of MDI to THPO 1: 0.8) are reduced by 83.6% and 33.0% compared to those of pure PMMA. For PMMA-1.1 and PMMA-1.25, the heat, smoke and toxic gas release are all decreased effectively, which indicates improvement of fire safety of PMMA. The PHRR, THR, total smoke production (TSP) and CO yield (COY) of PMMA-1.1 are decrease by 83.3%, 11.0%, 27.6% and 34.8%, respectively. In the back temperature test, PMMA-0.95 and PMMA-1.1 have the lowest back temperature rise rates in HPUPO coated PMMA, and the back temperature are about 200 °C under the continuous burning of the alcohol lamp for 800 s. In summary, PMMA-1.1 shows excellent transparency, adhesion and fire safety. HPUPO coated PMMA is a promising fire safe PMMA material for practical application and HPUPO can be used as transparent flame retardant coating with tailorable properties. [Display omitted] • A transparent flame retardant coating for PMMAwas prepared with hyperbranched poly(urethane-phosphine oxide). • The HPUPO coatings show a strong adhesion and high transparency. • The HPUPO coatings can effectively improve the fire safety of PMMA. [ABSTRACT FROM AUTHOR]

[Display omitted] • Phosphorylated cardanol-based oligomers were synthesized for flame-retardant and toughened epoxy. • The elongation at break of the treated epoxy was 133.3% higher than that of neat epoxy. • The peak heat release rate of the treated epoxy was 53.8% lower than pure epoxy. • The residual yield of EP/CF-PO(OPh) 2 –10 under nitrogen was 52.7% higher than that of pure epoxy. • Cardanol-based oligomer with higher phosphorus oxidation state showed better flame-retardant efficiency. Presently, flammability and brittleness are two major problems for EP which has restricted its development and application in industrial. Under the global advocacy of green and sustainable development, developing bio-based flame-retardant and toughening agents which can endow epoxy resins with high fire resistance and satisfactory mechanical properties is of significant demand for its industrial applications. Herein, three kinds of phosphorylated cardanol-formaldehyde oligomers (CF-PO(OPh) 2 , CF-POPh 2 , and CF-PPh 2) were synthesized and introduced into epoxy thermosets. The incorporation of CF-PO(OPh) 2 , CF-POPh 2 , and CF-PPh 2 can remarkably improve the mechanical performance of EP composites, especially the tensile strength and elongation at break. With 10 wt% of CF-PO(OPh) 2 , CF-POPh 2 , and CF-PPh 2 , the tensile strength of epoxy thermosets reached 67.1, 74.5, and 70.3 MPa, respectively; the elongation at break of epoxy thermosets was raised by 133.3%, 162.5%, and 150.0%, respectively, as compared to neat EP. EP composites containing CF-PO(OPh) 2 , CF-POPh 2 , and CF-PPh 2 also exhibited remarkably enhanced flame retardancy simultaneously. Besides, CF-PO(OPh) 2 exhibited the best flame-retardant efficiency by comparison with CF-POPh 2 and CF-PPh 2 , and the results manifested that epoxy composite with only 2.5 wt% CF-PO(OPh) 2 could pass the UL-94 V-0 rating as well as a high LOI value of 28%, and the LOI value of EP/CF-PO(OPh) 2 –10 reached up to 32%. Moreover, CF-PO(OPh) 2 also displayed an excellent catalytic charring effect and great suppression effect on heat and smoke release. The cone calorimeter test results showed that EP composite containing 10 wt% CF-PO(OPh) 2 exhibited the most significant PHRR reduction which was 53.8% lower than pure EP, and the char yield of EP/CF-PO(OPh) 2 –10 after the cone calorimeter test was 14.0% which was much higher than that of pure EP (5.7%). This work opens a new vision for the synthesis of bio-based flame-retardant and toughening agents with a special oligomeric structure combining rigidity with flexibility, and contributes to the production of high-performance epoxy thermosets. [ABSTRACT FROM AUTHOR]

Nowadays, highly flexible, ultrathin, and conductive polymer composites are exceptionally desirable for electromagnetic interference shielding (EMI) applications due to their unique mechanical strength and electrical and flame-resistant properties. While the traditional nanocomposites blending remains the mainstream method to fabricate polymer/inorganic composites, it results in poor electrical conductivity caused by the discontinuous connection of conductive network as well as the unsatisfactory mechanical strength limiting the further practical applications. Herein, we introduce a facile and practical methodology involving the fabrication of self-interlocked poly (vinyl alcohol) (PVA) and conductive Ti 3 C 2 T x MXene networks, then combining them to construct a nanostructure-engineered PVA/MXene membrane. This membrane exhibits superior mechanical strength, in which the tensile strength is about three times higher than the control PVA. Additionally, the membrane demonstrates outstanding fire-resistant performances with an 80% reduction of peak heat release rate than pure PVA. More importantly, this unique membrane with random conductive networks possesses an outstanding EMI shielding efficiency near 41 dB much greater than traditional composite, which meets the requirement of high-efficiency EMI shielding applications. This article displays a novel strategy to fabricate a nanostructured polymer membrane with outstanding fire resistance, electrical conductivity, and mechanical strength, targeted and designed for high-efficiency EMI shielding applications. [ABSTRACT FROM AUTHOR]

There are many applications for epoxy resin as a coating material in the automotive, electronics, and aerospace industries. However, when derived from petrochemical industries, adversely affect the environment, as they are rigid and resistant to recycling due to inherent cross-linked structure. In the present study, we prepared green epoxy resin from renewable resources, able to replace the conventionally produced DGEBA thermoset. Initially, we synthesized an epoxy thermoset from vanillin-derived Schiff base epoxy monomer (VTA-EP) that was thermally cured with bio-based 5, 5′-methylenedifurfurylamine (DFA). Due to the unsaturated double bond in cured VTA-EP/DFA thermoset displayed a relatively high glass transition temperature (T g ~ 170 °C) than the DGEBA/DDM system. Also, tensile strength (60 MPa), storage modulus (3271 MPa), and elongation at break (2.8%) were higher. Additionally, the peak of heat release rate (PHRR) and the total heat release (THR) of the cured VTA-EP/DFA resin decreased, and LOI and UL-94 ratings were improved. The green epoxy thermoset exhibited good dissolution in various acidic conditions due to the degradability of the Schiff base network in contrast to DGEBA/DDM. This work demonstrates that the combination of biomass with Schiff base structure provides a versatile platform for the fabrication of multifunctional vanillin-derived epoxy thermosets. [Display omitted] • A fully bio-based epoxy resin derived from vanillin was synthesized. • The fully bio-based epoxy resin system showed excellent intrinsic flame retardancy. • The fully bio-based epoxy resin possessed excellent acidity and temperature-controlled degradability. [ABSTRACT FROM AUTHOR]