有机磷系化合物反应阻燃聚乳酸的机理与性能

介绍9,10-二氢-9-氧杂-10-磷杂菲-10-氧化物(DOPO)及其衍生物10-(2,5-二羟基苯基)-10-氢-9-氧杂-10-磷杂菲-10-氧化物(DOPO-HQ)分别反应阻燃聚乳酸(PLA)的机理和对PLA力学性能、阻燃性能、耐热性能的影响。结果表明,少量DOPO对PLA有良好的阻燃效果,少量过氧化二异丙苯(DCP)与DOPO-HQ并用能有效改善PLA的阻燃性能和热稳定性能。5%DOPO-HQ/0.5%DCP阻燃PLA具有良好的综合性能,拉伸强度为49.37MPa,断裂伸长率为5.03%,氧指数为32%,试样热失重5%、50%时的温度分别提高38、36℃。     

改性凹凸棒土对PBAT阻燃性能的影响

用费托蜡（FTW）对凹凸棒土（ATP）进行表面改性制备了阻燃剂F-ATP，并对其形貌、结构及其热稳定性进行了表征。将阻燃剂F-ATP加入到聚己二酸/对苯二甲酸丁二醇酯（PBAT）基体中制备了PBAT/F-ATP复合材料。采用极限氧指数测定仪（LOI）、垂直燃烧测试（UL-94）、锥形量热仪（CCT）、TG-IR、拉曼光谱仪和SEM对复合材料的阻燃性能进行了分析。结果表明，改性后的ATP团聚现象消失且热稳定性明显提高。阻燃剂F-ATP质量分数为10%的PBAT/F-ATP复合材料（PBAT-3）阻燃效果最佳，其LOI值达到23.5%,UL-94等级达到V-1级，熔滴现象得到明显改善。与ATP质量分数为10%的PBAT/ATP复合材料相比，PBAT-3复合材料的峰值热释放速率值（PHRR）、总热释放量（THR）分别降低了4.99%和26.11%。PBAT-3复合材料气态产物的释放量在整个燃烧过程中均降低，起到了很好的气相阻燃效果，这主要归因于阻燃剂F-ATP的加入使PBAT/F-ATP复合材料形成致密且连续性好的炭层结构，有效地隔绝了复合材料内部与外界的热量/质量传递。     

Rheological and mechanical behavior of non-spherical poly(lactic acid) particles embedded poly(butylene adipate-co-terephthalate) blend

In this study, the poly(lactic acid) (PLA)/poly(butylene adipate-co-terephthalate)(PBAT) blend is investigated to improve rheological and mechanical performances of PBAT based on rheological, mechanical, and thermal behavior analyses. The multi-step mixing method is developed to fabricate the blend with non-spherical morphology. In the multi-step mixing method, blends with a wide composition range (25/75–75/25) are mixed with additional PBAT at a mixing temperature between the melting temperatures of PBAT and PLA to produce the PBAT blend embedded with non-spherical PLA particles (10 wt%). The embedding of non-spherical PLA particles in PBAT increases the resistance against deformation, resulting in strain hardening behavior and an increase in the yield strength as well as the tear resistance of the PBAT. The presence of stiff PLA particles enhances the crystallization behavior of PBAT, meaning that polymer chains may interpenetrate. The findings of this study suggest that the multi-step mixing method is beneficial for embedding non-spherical PLA particles into a PBAT matrix, which in turn facilitates the maintenance of good interfacial adhesion to increase the melt strength, yield strength, and tear resistance.     

An effective flame retardant for poly(ethylene terephthalate) synthesized by phosphaphenanthrene and cyclotriphosphazene

A novel flame retardant [9,10‐Dihydro‐9‐oxa‐10‐phosphaphenanthrene‐10‐oxideÔtriphosphazene (DOPO–TPN)] based on phosphaphenanthrene and cyclotriphosphazene was synthesized and used to improve the flame retardancy of poly(ethylene terephthalate) (PET). The structure of DOPO–TPN was characterized by nuclear magnetic resonance, Fourier transform infrared spectroscope (FTIR), and elemental analysis. PET/DOPO–TPN composites with different amount of DOPO–TPN were prepared and the flame retardancy was determined by limiting oxygen index (LOI) and vertical burning test (UL‐94). With the incorporation of 5 wt % DOPO–TPN, the composite achieved a LOI value of 34% and UL‐94 V‐0 rating. The thermal properties of the PET/DOPO–TPN composites were investigated by thermogravimetric analysis. The flame retardant mechanism was investigated by pyrolysis‐gas chromatography/mass spectrometry (Py‐GC/MS), FTIR, and scanning electron microscopy (SEM). The Py‐GC/MS results showed that DOPO based fragments would exist in the gas phase during the pyrolysis of PET/DOPO–TPN composites which demonstrated that DOPO–TPN could act through gas‐phase action to exert flame retardant effect. The results of FTIR and SEM demonstrated that DOPO–TPN could promote the formation of compact and intact char residues to inhibit the heat and combustible gas transmission in condensed phase. © 2017 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2017 , 134, 45246.     

Influence of ammonium polyphosphate on the flame retardancy and mechanical properties of ramie fiber‐reinforced poly(lactic acid) biocomposites

Fully degradable natural fiber/degradable polymer composites have received much research attention and have various applications such as in automotive components. But flammability limits their application; it is important to improve the flame retardancy of fully degradable composites with environmentally friendly flame retardants. Flame‐retarded ramie fiber‐reinforced poly(lactic acid) (PLA) composites were prepared using three processes: (1) PLA was blended with ammonium polyphosphate (APP), and then the resulting flame‐retarded PLA was combined with ramie fibers; (2) ramie fibers underwent flame‐retardant treatment with APP, which were then compounded with PLA; and (3) PLA and ramie, both of which had been flame‐retarded using APP, were blended together. The APP in the composites is shown to be very effective in improving flame retardancy according UL94 test and limiting oxygen index measurements. Thermogravimetric analysis shows that the improved flame retardancy is due to increased char residue at high temperature. The loading of APP disturbs the compatibility between PLA and fibers, which can be directly observed using scanning electron microscopy. Furthermore it has an influence on the dynamic mechanical properties and mechanical properties according dynamic mechanical analysis and mechanical measurements. The results show that composites produced using the third process not only have the best flame retardancy but also comparatively better mechanical properties. Copyright © 2009 Society of Chemical Industry     

Improve the mechanical property and flame retardant efficiency of the composites of poly(lactic acid) and resorcinol di(phenyl phosphate) (RDP) with ZnO‐coated kenaf

The kenaf coated with zinc oxide (ZnO) was prepared and characterized by X‐ray diffraction, scanning electron microscopy, and X‐ray photoelectron spectroscopy. The ZnO‐coated kenaf and the flame retardant resorcinol di(phenyl phosphate) were blended with poly(lactic acid) (PLA) by solution compounding and melt blending to prepare the flame‐retarded PLA composites. The thermal stability, the mechanical property, and the flame retardancy of the PLA composites were improved evidently. The tensile strength of the prepared PLA composites could reach up to 62.3 MPa in comparison with 55.4 MPa of the pure PLA. The dense and compact char residues were observed after the combustion of the PLA composites containing ZnO‐coated kenaf, whereas there were serious dripping phenomena and no char formation during the combustion of the pure PLA. The use of ZnO‐coated kenaf could increase flame retardant efficiency obviously. The mechanism of flame retardancy was discussed. Copyright © 2014 John Wiley & Sons, Ltd.     

Compatible and crystallization properties of poly(lactic acid)/poly(butylene adipate‐co‐terephthalate) blends

Differential scanning calorimetry (DSC), wide angle X‐ray diffraction (WAXD) and dynamic mechanical analysis (DMA) properties of poly(lactic acid)/ poly(butylene adipate‐co‐terephthalate) (PLA/PBAT) specimens suggest that only small amounts of poor PLA and/or PBAT crystals are present in their corresponding melt crystallized specimens. In fact, the percentage crystallinity, peak melting temperature and onset re‐crystallization temperature values of PLA/PBAT specimens reduce gradually as their PBAT contents increase. However, the glass transition temperatures of PLA molecules found by DSC and DMA analysis reduce to the minimum value as the PBAT contents of PLA_xPBAT_y specimens reach 2.5 wt %. Further morphological and DMA analysis of PLA/PBAT specimens reveal that PBAT molecules are miscible with PLA molecules at PBAT contents equal to or less than 2.5 wt %, since no distinguished phase‐separated PBAT droplets and tan δ transitions were found on fracture surfaces and tan δ curves of PLA/PBAT specimens, respectively. In contrast to PLA, the PBAT specimen exhibits highly deformable properties. After blending proper amounts of PBAT in PLA, the inherent brittle deformation behavior of PLA was successfully improved. Possible reasons accounting for these interesting crystallization, compatible and tensile properties of PLA/PBAT specimens are proposed. © 2009 Wiley Periodicals, Inc. J Appl Polym Sci, 2010     

Preparation,characterization and properties of a halogen‐free phosphorous flame‐retarded poly(butylene terephthalate) composite based on a DOPO derivative

A phosphorous flame retardant (DOPO‐MAH) was synthesized through the reaction between of 9,10‐dihydro‐9‐oxa‐10‐phosphaphenanthrene‐10‐oxide (DOPO) and maleic anhydride (MAH) and confirmed by FT‐IR, ¹H NMR, and ³¹P NMR techniques. The obtained flame retardant was then melt blended with poly(butylene terephthalate) (PBT) to prepare flame retardant PBT/DOPO‐MAH composites. The composites were characterized by LOI, UL‐94, and mechanical tests as well as scanning electron microscopy, thermogravimetric analysis, and differential scanning calorimetry analysis. On adding 20 wt % DOPO‐MAH, LOI increased from 20.9 to 25.7 and the UL‐94 V‐0 rating was achieved, whereas the tensile and flexural properties were notably improved. Torque‐time profile during the melt blending and intrinsic viscosity of the composite indicated that DOPO‐MAH acted as both flame retardant and chain extender for the PBT matrix. The results showed that PBT/DOPO‐MAH composite is a promising material for its good comprehensive properties. © 2013 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 130: 1301‐1307, 2013     

聚己内酯对聚乳酸/PBAT共混物增容作用的研究

研究了聚己内酯(PCL)作为增容剂对聚乳酸(PLA)与聚己二酸-对苯二甲酸丁二酯(PBAT)的共混物力学性能、热性能、动态力学性能和相容性的影响。结果表明,加入PCL可以改善PLA与PBAT的相容性,提高共混物的冲击强度、拉伸强度和拉伸弹性模量;在PCL含量为2份时共混物两相之间具有良好的相容性。     

Facile and scalable fabrication of bioderived flame retardant based on adenine for enhancing fire safety of fully biodegradable PLA/PBAT/TPS ternary blends

The facile fabrication of a bioderived flame retardant (marked as ATMP-A) via ionic exchange between adenine and amino trimethylene phosphonic acid was reported in the present work. The incorporation of ATMP-A endows the poly lactic acid (PLA)/poly butylene adipate-co-terephthalate (PBAT)/thermoplastic starch (TPS) ternary blends with improved fire safety without negatively affecting the biodegradability. The PLA/PBAT/TPS blend containing 18 wt% ATMP-A alone achieves a UL-94 V-0 rating with a higher LOI value (28%). Meanwhile, its peak of the heat release rate and total heat release are reduced by 60.5% and 34.1% as compared with the PLA/PBAT/TPS ternary blend, respectively. Such excellent flame retardancy is mainly attributed to the formation of the intumescent flame retardant system in which ATMP-A acts as both acid and gas sources together with TPS as a natural carbon source. Based on the analysis of the volatile gases and the char residues, a possible flame retardant mechanism including gas phase and condensed phase is proposed. This work provides a novel and effective idea for improving the fireproof performance of PLA/PBAT/TPS blends and will broaden its practical application fields, such as, agricultural film and packaging fields.     

Improving the flame retardance and melt dripping of poly(lactic acid) with a novel polymeric flame retardant of high thermal stability

A polymeric flame retardant containing phosphorus and nitrogen (PCNFR) was synthesized and characterized by Fourier transform infrared spectroscopy, nuclear magnetic resonance and gel permeation chromatography. The thermal decomposition temperatures at 10% weight loss (T_{10 wt%}) of PCNFR were around 358 °C, and the char yield at 600 °C reached about 60 wt% both in nitrogen and air by thermogravimetric analysis. The flame retarded poly(lactic acid) (PLA) composites with PCNFR were prepared. The thermogravimetric analysis results showed that PCNFR could improve the thermal stability of the flame retarded PLA composites with low loading (≤10 wt%) and at high temperature zone (≥390 °C). The condensed products from the decomposition of the flame retarded composites at 380 °C and 450 °C for different intervals were analyzed by Raman spectroscopy, and the results showed that time and temperature influenced the structure of the char residue evidently. When incorporating 30 wt% PCNFR into PLA, the limited oxygen index of the flame retarded composites reached 25.0%, and V‐0 rating was achieved. The char residues were analyzed by scanning electron microscopy, Fourier transform infrared spectroscopy and X‐ray photoelectron spectroscopy in detail. Copyright © 2016 John Wiley & Sons, Ltd.     

Development of ductile green flame retardant poly(lactic acid) composites using hydromagnesite&huntite and bio-based plasticizer

Turning brittle poly(lactic acid) (PLA) to ductile form via plasticizer inclusion is an effective option in the case of processing with high amounts of additives. Additionally, the integration of natural flame retardants to PLA involving bio-based plasticizer enables to use of environmentally friendly composites in conditions where fire resistance performance is required. In the current study, ductile green fire retardant PLA composites were manufactured using hydromagnesite&huntite (HH) as a natural fire retardant additive and acetyl tributyl citrate as a bio-based plasticizer. The influences of plasticizer and HH contents on the fire retardant, thermal and mechanical performances of the composites were explored. According to test results, the limiting oxygen index (LOI) value of PLA reduced from 29.2 to 28.0 and the UL-94 V rating changed from V2 to BC with the addition of 20 wt% plasticizer owing to the reduction in melt viscosity. The peak heat release rate (pHRR) and average heat release rate (avHRR) values increased steadily as the concentration of plasticizer increased due to the formation of a more porous residue structure stemming from the increased transportation rate of gases. In order to produce ductile flame retardant material, the plasticizer content was required to 20 wt% of HH. The highest LOI value (36.2) and UL-94 rating of V0 were achieved with the inclusion of 70 wt% HH in the presence of 20 wt% plasticizer. Improvement in impact resistance and reduction in tensile strength were observed as the added amount of plasticizer increased.     

Polylactic acid flame-retardant composite preparation and investigation of flame-retardant characteristics

Polylactic acid (PLA) is a new type of biodegradable material with good mechanical properties, and is widely used in many fields. However, as PLA is highly flammable, it is necessary to conduct flame-retardant modification research on PLA. Phosphorus heterophilic flame retardants are low smoke, non-toxic and have high flame-retardant efficiency, and also have broad application prospects. In this study, a phosphazene flame retardant, 9,10-dihydro-9-oxa-10-phosphazene-10-yl-hydroxy-phenol (abbreviated as DOPO-PHBA), was synthesized. The PLA/ECE/DOPO-PHBA flame-retardant composites were prepared by adding DOPO-PHBA and epoxy chain extender (ECE) into PLA. Thermal, mechanical, and flame-retardant properties, as well as microscopic morphology of the PLA flame-retardant composites were characterized and analyzed, and the flame-retardant mechanism was discussed. Results show that when the flame-retardant DOPO-PHBA is added at 5 wt%, the PLA composites can reach the V-0 level of combustion, and the corresponding LOI value is 30.0% at this time, and the LOI value increases from 22.5% to 33.6% with the increase of the flame-retardant content. In addition, PLA composites still have good mechanical properties, and the cone heat, carbon residue and the thermal decomposition process shows that the flame-retardant causes a two-phase flame-retardant mechanism on PLA with the gas and condensed phases acting in synergy. High flame retardancy is mainly attributed to free radical quenching, gas dilution, and the thermal barrier caused by the carbon layer. This work provides a simple and scalable method for the preparation of high-performance flame-retardant PLA materials.     

A novel phosphorus-containing poly(lactic acid) toward its flame retardation

An inherently flame-retardant poly(lactic acid) (PLA) was synthesized via the chain-extending reactions of dihydroxyl terminated pre-poly(lactic acid) (pre-PLA), which was synthesized by direct polycondensation of l-lactic acid using 1,4-butanediol as initiator and stannous chloride (SnCl₂) as catalyst, using ethyl phosphorodichloridate as chain extender. The resulting phosphorus-containing poly(lactic acid) (PPLA) was characterized by gel permeation chromatography (GPC), ¹H and ³¹P nuclear magnetic resonance (¹H, ³¹P NMR) and homonuclear correlation spectroscopy (COSY) and inductively coupled plasma-mass (ICP). A comprehensive flame retardant property of PPLA was evaluated by microscale combustion calorimetry (MCC), limiting oxygen index (LOI), vertical burning test (UL-94) and cone calorimeter test (CCT). PPLA has excellent flame retardancy and also can be used as a flame retardant for commercial PLA. Only 5 wt.% of PPLA added into PLA can obtain good flame retardant properties. As the content of PPLA is further increased to 10 wt.%, PLA can have much better flame retardancy (LOI = 35 and UL-94 V-0 rating), lower peak heat release rate (pHRR) and longer ignition time (TTI) than neat PLA. All those results mean that this novel approach to impart flame retardancy to PLA is very effective.     

Improvement of the flame retardancy of plasticized poly(lactic acid) by means of phosphorus‐based flame retardant fillers

The aim of this study is to improve the flame resistance and toughness of poly(lactic acid) (PLA) with the addition of low amount of flame retardant fillers and plasticizer simultaneously. Poly(ethylene glycol) (PEG) was used as plasticizer for PLA. Ammonium polyphosphate, boron phosphate, and tri‐phenyl phosphate (TPP) were used as flame retardant additives. Among these flame retardant additives, boron phosphate was synthesized from its raw materials by using microwave heating technique. Characterization of PLA/PEG‐based flame retardant composites was performed by conducting tensile, impact, differential scanning calorimeter, thermal gravimetric analysis, scanning electron microscope, limiting oxygen index, and UL‐94 vertical burning tests. Mechanical tests showed that the highest tensile strength, impact strength, and elongation at break values were obtained with the addition of ammonium polyphosphate and TPP into PLA/PEG matrix, respectively. Scanning electron microscopy analysis of the composites exhibited that the more homogeneous filler distribution in the matrix was observed for TPP containing composite. The best flame retardancy performance was also provided by TPP when compared with the other flame retardant additives in the plasticized PLA‐based composites.     

Effects of ammonium polyphosphate and triphenyl phosphate on the flame retardancy,thermal, and mechanical properties of glass fiber–reinforced PLA/PC composites

The purpose of this study is to increase of the flammability properties of the glass fiber (GF)–reinforced poly (lactic acid)/polycarbonate (PLA/PC) composites. Ammonium polyphosphate (APP) and triphenyl phosphate (TPP) were used as flame retardants that are including the organic phosphor to increase flame retardancy of GF‐reinforced composites. APP, TPP, and APP‐TPP mixture flame retardant including composites were prepared by using extrusion and injection molding methods. The properties of the composites were determined by the tensile test, limiting oxygen index (LOI), differential scanning calorimetry (DSC), and heat release rate (HRR) test. The minimum T_g value was observed for the TPP including PLA/PC composites in DSC analysis. The highest tensile strength was observed in GF‐reinforced PLA/PC composites. In the LOI test, GF including composite was burned with the lowest concentration of oxygen, and burning time was the longest of this composite. However, the shortest burning time was obtained by using the mixture flame retardant system. The flame retardancy properties of GF‐reinforced PLA/PC composite was improved by using mixture flame retardant. When analyzed the results of HRR, time to ignition (TTI), and mass loss rate together, the best value was obtained for the composite including APP.     

Influence of phthalic anhydride and bioxazoline on the mechanical and morphological properties of biodegradable poly(lactic acid)/poly[(butylene adipate)‐co‐terephthalate] blends

Poly(lactic acid) (PLA)/poly[(butylene adipate)‐co‐terephthalate] (PBAT) blends were fabricated by melt blending, with 2,2′‐(1,3‐phenylene)bis(2‐oxazoline) (BOZ) and phthalic anhydride (PA) used as compatibilizers. It was found that a small amount of BOZ or PA greatly increased the elongation at break of the PLA/PBAT blends without sacrificing their high tensile strength. Scanning electron microscopy results revealed that the PBAT particles became finer and were uniformly dispersed in the matrix when the compatibilizers were incorporated, which indicated that the interfacial bonding and compatibilization between PLA and PBAT were improved in the presence of the compatibilizers. Compared with PLA/PBAT blends, the molecular weight of PLA/PBAT/PA/BOZ blends was increased due to chain‐extending reactions. Differential scanning calorimetry results suggested PBAT decreased the crystallization rate and crystallinity of PLA in the blends. Moreover, the glass transition temperature of PBAT was further decreased when the compatibilizers were used. © 2013 Society of Chemical Industry     

Facile fabrication of highly flexible poly(lactic acid) film using alternate multilayers of poly[(butylene adipate)‐co‐terephthalate]

Poly(lactic acid) (PLA) and poly[(butylene adipate)‐co‐terephthalate] (PBAT) are both commonly used biodegradable polymers. In this study, co‐extrusion of PLA and PBAT was used to create alternately multilayered films in order to obtain high‐flexibility PLA film. The incorporation of PBAT provides enhanced flexibility to PLA and the effect is more distinct in the PLA/PBAT multilayer film as the number of layers increases. Through differential scanning calorimetric and wide‐angle X‐ray scattering analyses, the crystallinity of PLA is shown to decrease more in the multilayer film than in the blended film. Transparency is also enhanced in the multilayer film. The fabrication of alternate multilayered film by co‐extrusion of PLA and PBAT shows a new method of preparing a flexible, transparent and fully biodegradable film, which is impossible through a blending process. © 2014 Society of Chemical Industry     

Flame retardant performance of a carbon source containing DOPO derivative in PET and epoxy

The combination of gas‐phase and condensed‐phase action will contribute to high quality flame retardant. A novel 9,10‐dihydro‐9‐oxa‐10‐phosphaphenanthrene‐10‐oxide (DOPO)‐based flame retardant (DOPO‐DOPC), which contains carbon source was synthesized in favor of conducting the effect of gas‐phase as well as promoting the char formation in condensed‐phase. The chemical structure of DOPO‐DOPC was characterized by nuclear magnetic resonance (NMR) and Fourier transform infrared spectroscopy (FTIR). DOPO–DOPC was used as an additive in poly(ethylene terephthalate) (PET) and epoxy resin (EP). The flame retardancy of PET/DOPO‐DOPC and EP/DOPO‐DOPC composites were studied by limiting oxygen index (LOI) and UL‐94 test. The results showed that the incorporation of DOPO–DOPC into PET or EP could obviously improve their flame retardancy. The LOI values of modified PET or EP, which contained 10 wt % DOPO‐DOPC reached 42.8 and 31.7%, respectively. The thermogravimetric analysis (TGA) results revealed that DOPO–DOPC enhanced the formation of char residues. The Laser Raman spectroscopy (LRS) was used to investigate the carbon structure of thermal oxidation residues. Because of the combination of the gas phase flame retardant effect of DOPO moiety and the promoting formation of char residues in condensed phase, the PET and EP composites exhibited significant improvement toward flame retardancy. © 2016 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2017 , 134, 44639.     

四元复合体系在硬质聚氨酯泡沫材料中的逐级释放阻燃行为研究

以甲基膦酸二甲酯（DMMP）、10?（2,5?二羟基甲苯）?10?氢?9?氧杂?10?磷酰杂菲?10?氧化物（DOPO?HQ）、可膨胀石墨（EG）和氢氧化铝（ATH）构建了四元阻燃复合体系,并通过热失重分析仪（TG）、锥形量热仪、极限氧指数分析仪等研究了其在硬质聚氨酯泡沫（RPUF）中的阻燃行为。结果表明,四元阻燃体系能够在较宽温度区间内发挥逐级释放的协同阻燃效应;DOPO?HQ能够与EG/DMMP/ATH三元阻燃体系形成加合阻燃效应,使得RPUF复合材料的极限氧指数（LOI）提升至30.8 %;与采用EG/DMMP/ATH三元阻燃体系的RPUF复合材料相比,采用加入DOPO?HQ的四元阻燃体系的RPUF复合材料的热释放速率峰值（PHRR）、总热释放量（THR）、总烟释放量（TSR）均有所下降,残炭率得到了进一步提升,说明DOPO?HQ与EG/DMMP/ATH所构建的四元阻燃体系在成炭性方面具有协同效应;此外,通过扫描电子显微镜（SEM）对残炭进行表征,验证了四元阻燃体系在凝聚相中能够发挥优异的成炭阻隔效应,并能够在燃烧的初期、中期和末期发挥逐级释放阻燃效应。