Improving the flame‐retardant efficiency of aluminum hydroxide with fullerene for high‐density polyethylene

The influence of fullerene (C₆₀) on the flame retardancy and thermal stability of high‐density polyethylene (HDPE)/aluminum hydroxide (ATH) composites was studied. After the addition of three portions of C₆₀ to an HDPE–ATH (mass ratio = 100:120) composite, a V‐0 rating in the UL‐94 vertical combustion test was achieved, and the limiting oxygen index increased by about 2%. The results of cone testing also showed that the addition of C₆₀ effectively extended the time to ignition and the time to maximum heat‐release rate while cutting down the peak heat‐release rate. Thus, fewer flame retardants were needed to achieve a satisfactory flame retardance. Consequently, the adverse effects on the mechanical properties because of the high level of flame‐retardant loading was reduced, as evidenced by the obvious enhancements in the tensile strength, elongation at break, and flexural strength. Electron spin resonance spectroscopy proved that C₆₀ was an efficient free‐radical scavenger toward HO· radicals. Thermogravimetric analysis coupled to Fourier transform infrared spectroscopy demonstrated that in both N₂ and air atmospheres, C₆₀ increased the onset temperature of the matrix by about 10 °C because of its enormous capacity to absorb free radicals evolved from the degradation of the matrix to form crosslinked network, which was covered by aluminum oxide. © 2016 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2017 , 134, 44551.     

用锥形量热仪研究无卤阻燃HDPE体系的燃烧性

在35kW／m^2热辐照条件下,利用锥形量热仪研究了膨胀型阻燃剂／Mg(OH)2阻燃高密度聚乙烯(HDPE)体系的燃烧性。结果表明：膨胀型阻燃剂／Mg(OH)2能明显降低HDPE的热释放速率、总热释放量、最大生烟速率及总烟释放量。与膨胀型阻燃剂单独使用相比,Mg(OH)2与膨胀型阻燃剂复合使用的阻燃效果明显,总烟释放量减少了38％,总热释放量减少了10％,达到了低发炯、高效阻燃的目的。     

Synergistic flame retardancy of tris(1-methoxy-2,2,6,6-tetramethyl-piperidin-4-yl)phosphite and tris(2,4,6-tribromophenoxy)-1,3,5-triazine/Sb2O3 in high-impact polystyrene

Synergistic flame retardancy of tris(1-methoxy-2,2,6,6-tetramethyl-piperidin-4-yl) phosphite (NORPM) and tris(2,4,6-tribromophenoxy)-1,3,5-triazine (TTBPC)/Sb₂O₃ in high-impact polystyrene (HIPS) was studied by limiting oxygen index (LOI) determination, UL-94 test, and cone calorimetry test (CCT). NORPM has an exceptional synergistic effect in HIPS. When the dosage of TTBPC, Sb₂O₃, and NORPM was 12.8, 3.2, and 0.5 wt% respectively, flame retardant effectivity and synergistic effectivity were 0.424 and 1.15 respectively. Compared with the Flame retardant (FR)-HIPS containing 16.0 wt% of TTBPC/Sb₂O₃, the LOI of FR-HIPS increases from 23.8% to 25.4%, the flame-retardant rating of FR-HIPS can be improved from UL 94 V-2 to V-0, and the peak heat release rate and total heat release are significantly reduced by combining NORPM in 0.5 wt% concentration. NORPM induces the synergistic effect mainly through the following mechanisms: the active radicals produced by the pyrolysis of NORPM promote the release of bromine radicals from TTBPC and the formation of HBr, which improves the flame retardancy of TTBPC; the above active radicals, together with HBr, quench active free radicals, such as the hydroxyl radical (·OH) and decompose the free radical source, which interrupts the chain reaction during combustion and results in a more efficient flame retardant effect in gaseous phase.     

Synthesis of FePP@MoS2@Ni-MOF composites for improving thermal and flame retardant safety properties of polyurea

Polyurea (PUA) is widely used as a coating in construction, tunnels, bridges, and other fields because of its excellent performance. However, its combustion emits toxic gases and smoke, hindering escape and posing potential fatality risks. Enhancing the flame retardancy of PUA is crucial for safety and expanding its applications. The synthesis of two-dimensional FePP nanosheets was reported in this paper, employing the solvothermal method, followed by the sequential growth of MoS₂ and Ni-MOF to establish a multilayer composite structure. The elemental composition and morphology of the synthesized FePP@MoS₂@Ni-MOF flame retardants were characterized and analyzed. The flame retardant properties of polyurea composites with varying amounts of FePP@MoS₂@Ni-MOF were investigated using Cone calorimeter tests. The results showed that the prepared flame retardant had good thermal stability and significantly improved fire safety properties. The PUA/FePP@MoS₂@Ni-MOF 3.0 composite exhibited notable improvements compared to pure PUA. Specifically, the peak heat release rate, total heat release rate and peak smoke production rate were reduced by 39.76%, 29.33% and 17.86%, respectively, while total smoke production and total CO production (COP) were reduced by 21.30% and 54.47%. This study provides new insights and experimental basis for the technological development of novel flame retardant coating materials.     

Influence of char-forming lignin in combination with aluminium phosphinate on thermal stability and combustion properties of polyamide 11 blends

Polyamide 11 (PA) blends based on char-forming industrial lignin and aluminum phosphinate (AlP) were prepared to improve flame retardant (FR) properties using a green and eco-friendly approach. This study investigates the thermal degradation and combustion behavior of PA blends prepared by using AlP in combination with two different types of industrial lignins (i.e., kraft lignin (DL) and lignosulphonate lignin (LL). Thermogravimetric (TG) analysis showed that ternary blends containing LL and AlP developed higher char residue up to 10.7 wt% upon decomposition in inert atmospheres. The combination of lignin and AlP increases the thermal stability by shifting the initial decomposition temperature (T_5%) and temperature at maximum decomposition (T_max) to a higher temperature range, attributed to the stabilization of decomposition products. Furthermore, combustion behavior studied by cone calorimeter (forced combustion) and pyrolysis combustion flow calorimeter (PCFC) tests presented a significant reduction in the peak of heat release rate (PHRR) and total heat release (THR). It was found that LL and AlP-containing blends more effectively decreased fire parameters like PHRR and THR than that of DL and AlP-containing blends. The best interaction with reduced fire-retardant properties was obtained when 10 wt% loading of lignin (DL/LL) and AlP was used. The reduction in heat release parameters was mainly ascribed to the condensed phase mechanism by forming an efficient protective char layer, which acts as a barrier against heat and mass transfer between the condensed and the gas phases. Raman spectroscopy analysis also confirmed the formation of the protective graphitic layer in the condensed phase.     

Synergistic effects of fumed silica on intumescent flame‐retardant polypropylene

The synergistic effects of fumed silica on the thermal and flame‐retardant properties of intumescent flame retardant (IFR) polypropylene based on the NP phosphorus‐nitrogen compound have been studied by Fourier transfer infrared (FTIR) spectroscopy, cone calorimeter test (CCT), scanning electron microscopy (SEM), thermogravimetric analysis (TGA), limiting oxygen index (LOI), and UL‐94 tests. The LOI and UL‐94 data show that when ≤1 wt % fumed silica substituted for the IFR additive NP can increase 2 to 4% LOI values of the PP blends and keep the V‐0 rating. The data obtained from the CCT tests indicate the heat release rates (HRR) reduce by about 23% for the PP/NP sample with 0.5 wt % fumed silica, whereas the mass loss rates (MLR) and total heat release (THR) values are much lower than those of the PP/NP samples without fume silica. The TGA data demonstrate that a suitable amount of fumed silica can increase the thermal stability and charred residue of the PP/IFR/SiO₂ blends after 500°C. The morphological structures of charred residues observed by SEM give positive evidence that a suitable amount of fumed silica can promote the formation of compact intumescent charred layers and prevent the charred layers from cracking, which effectively protects the underlying polymer from burning. The dynamic FTIR spectra reveal that the synergistic flame‐retardant mechanism of a suitable amount of fumed silica with IFR additive is due to its physical process in the condensed phases. However, a high loading of fumed silica restricts the formation of charred layers with P? O? P and P? O? C complexes formed from burning of polymer materials and destroys the swelling behavior of intumescent charred layers, which deteriorates the flame retardant and thermal properties of the PP/IFR blends. © 2009 Wiley Periodicals, Inc. J Appl Polym Sci, 2010     

Preparation and investigation of flame‐retardant epoxy resin modified with a novel halogen‐free flame retardant containing phosphaphenanthrene,triazine‐trione,and organoboron units

In this article, a novel flame retardant (coded as BNP) was successfully synthesized through the addition reaction between triglycidyl isocyanurate, 9,10‐dihydro‐9‐oxa‐10‐phosphaphenanthrene‐10‐oxide and phenylboronic acid. BNP was blended with diglycidyl ether of bisphenol‐A to prepare flame‐retardant epoxy resin (EP). Thermal properties, flame retardancy, and combustion behavior of the cured EP were studied by thermogravimetric analysis, limited oxygen index (LOI) measurement, UL94 vertical burning test, and cone calorimeter test. The results indicated that the flame retardancy and smoke suppressing properties of EP/BNP thermosets were significantly enhanced. The LOI value of EP/BNP‐3 thermoset was increased to 32.5% and the sample achieved UL94 V‐0 rating. Compared with the neat EP sample, the peak of heat release rate, average of heat release rate, total heat release, and total smoke production of EP/BNP thermosets were decreased by 58.2%–66.9%, 27.1%–37.9%, 25.8%–41.8%, and 21.3%–41.7%, respectively. The char yields of EP/BNP thermosets were increased by 46.8%–88.4%. The BNP decomposed to produce free radicals with quenching effect and enhanced the charring ability of EP matrix. The multifunctional groups of BNP with flame retardant effects in both gaseous and condensed phases were responsible for the excellent flame retardancy of the EP/BNP thermosets. © 2017 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2017 , 134, 45291.     

Zinc hydroxystannate and zinc stannate as flame‐retardant agents for flexible poly(vinyl chloride)

The flame‐retardant and smoke‐suppressant properties of inorganic tin compounds such as zinc hydroxystannate (ZHS) and zinc stannate (ZS) were investigated in a comparison with alumina trihydrate, magnesium hydroxide, and Sb₂O₃ through the limiting oxygen index test and smoke density test. The flame‐retardant mechanisms were studied through the char yield test, SEM, quantitative analysis, thermogravimetry and differential thermal analysis. The thermal degradation in air of flexible PVC treated with the above compounds was studied by thermal analysis from ambient temperature to 800°C. The results showed that tin compounds such as ZHS and ZS could be used as a highly effective flame retardant for flexible PVC, and it appears that the tin compound may exert its action in both the condensed and vapor phases, but mainly in condensed phases as a Lewis acid. © 2005 Wiley Periodicals, Inc. J Appl Polym Sci 98: 1469–1475, 2005     

Flammability and thermal degradation of epoxy acrylate modified with phosphorus‐containing compounds

A series of UV‐curable flame‐retardant resins was obtained by blending phosphate acrylate (BTP) in different ratios with epoxy acrylate resin (EA). The flammability was characterized by limiting oxygen index (LOI), UL 94 flammability rating and cone calorimeter, and the thermal degradation of the flame‐retardant resins was studied using thermo gravimetric analysis (TGA), and real‐time Fourier transform infrared (RTFTIR). The results indicated that the flame‐retardant efficiency increases with the addition of BTP. The heat release rate with the addition of BTP decreases greatly. The TGA data showed that EA/BTP blends have lower initial decomposition temperatures and higher char residues than pure EA, whereas BTP has the lowest initial decomposition temperature and the highest char residue. The RTFTIR study indicates that the EA/BTP blends have lower thermal oxidative stability than the pure EA. © 2009 Wiley Periodicals, Inc. J Appl Polym Sci, 2010     

Synthesis of a novel organic–inorganic hybrid flame retardant based on Ca(H2PO4)2 and hexachlorocyclotriphosphazene and its performance in polyvinyl alcohol

To optimize the poor thermal stability and flammable of polyvinyl alcohol (PVA), a novel environmental-friendly organic–inorganic hybrid flame retardant Ca(H₂PO₄)₂@HCCP was successfully designed and synthesized via surface treatment technology and used to advance the flame retardancy of PVA. The thermogravimetric analysis implied that Ca(H₂PO₄)₂@HCCP can enhance significantly the thermal stability and char forming ability of PVA. Combustion results demonstrate that Ca(H₂PO₄)₂@HCCP could effectively suppress the melt dripping of PVA in the process of combustion. The presence of Ca(H₂PO₄)₂@HCCP can sharply reduce peak heat release rate and the total heat release up to 75% and 22.9%, respectively, in the microscale combustion calorimeter measurement. The results manifested that Ca(H₂PO₄)₂@HCCP could endow PVA with superior flame retardancy. Moreover, char residues analysis explained the flame retardant mechanism in condensed and gas phase, which is mainly attributed to the strong catalytic char formation, free radical trapping, and gas barrier effect. Therefore, the green flame retardant has great applications prospect in fire safety.     

Suppressing fire hazard of poly(vinyl alcohol) based on (NH4)2[VO(HPO4)]2(C2O4)·5H2O with layered structure

Two-dimensional layered ammonium vanadium oxalate-phosphates (AVOPh) with the structural formula of (NH₄)₂[VO(HPO₄)]₂(C₂O₄)·5H₂O are synthesized though a hydro-thermal method, which is dispersed into poly(vinyl alcohol) (PVA) matrix to prepare PVA/AVOPh composites. The results of thermal analysis indicate that AVOPh and PVA have similar decomposition temperature from 280 to 500°C, which is critical for choosing flame retardant. The incorporation of AVOPh significantly improves the thermal stability and flame retardancy of PVA/AVOPh composites that the T_5% value of PVA/2 wt% AVOPh composites is up to 215°C, and the residue of PVA/8 wt% AVOPh composites is enhanced to 16.9%, while those of pure PVA are only 178°C and 2.4%. PVA/4 wt% AVOPh composites can pass V-0 level, and its limiting oxygen index value is up to 32.0%. Furthermore, the peak heat release rate (PHRR) and total heat release (THR) of PVA/AVOPh composites are obviously decreased, which reduced by 43.4% and 43.8% with the addition of 4 wt% AVOPh, compared with those of pure PVA. The excellent thermal stability and flame retardancy are mainly attributed to the uniform dispersion and barrier effect of 2D layered AVOPh, the release of crystal water, ammonia and phosphorus free radicals and the two-phase flame retardant catalytic mechanism of vanadium and phosphorus.     

Flame‐retardant behavior of a phosphorus/silicon compound on polycarbonate

A phosphorus/silicon flame retardant, MVC‐DOPO, was synthesized from 9,10‐dihydro‐9‐oxa‐10‐phosphaphenanthrene‐10‐oxide (DOPO) and 2,4,6,8‐tetra‐methyl‐2,4,6,8‐tetra‐vinyl‐cyclo‐tetrasiloxane (MVC) via addition reaction. Its flame‐retardant effect on polycarbonate (PC) was investigated. The phosphorus/silicon flame retardant increased the limited oxygen index and UL‐94 rating and reduced the heat release rate and total heat release of DOPO‐MVC/PC composites during combustion, indicating the excellent flame‐retardant effect of MVC‐DOPO on PC. MVC‐DOPO inhibited the burning intensity of PC material in the gaseous phase and promoted the formation of a more viscous residue in the condensed phase. Through releasing phosphorus‐containing pieces and phenoxy radicals from the phosphaphenanthrene group, MVC‐DOPO quenched the combustion chain reaction in the gaseous phase; through promoting formation of a more viscous residue and a dense char layer from the main actions of the cyclotetrasiloxane group, MVC‐DOPO reduced fuel release and generated a barrier effect in the condensed phase. Hence, MVC‐DOPO effectively exerted a flame‐retardant effect on PC material in both the gaseous and condensed phases during combustion. © 2017 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2018 , 135, 45815.     

An efficient approach to improving fire retardancy and smoke suppression for intumescent flame‐retardant polypropylene composites via incorporating organo‐modified sepiolite

In this work, an efficient approach to improving the fire retardancy and smoke suppression for intumescent flame‐retardant polypropylene (PP) composites is developed via incorporating functionalized sepiolite (organo‐modified sepiolite [ONSep]). The PP composites with different amounts of intumescent flame retardants and ONSep were prepared by melt compounding. The morphology, thermal behavior, fire retardancy, smoke suppression, and mechanical property of flame‐retardant PP composites were studied. The results indicate an appropriate amount of ONSep in the flame‐retardant PP composites can increase thermal degradation temperature and char formation as well as a reduction of the peak heat release rate and total heat release; moreover, the addition of ONSep significantly decreases the CO production, total smoke production, smoke production rate, and smoke temperature. Simultaneously, the impact strength of intumescent flame‐retardant PP composite is also maintained by introducing an appropriate amount of ONSep as compared with that without ONSep.     

Effect of zinc oxide on properties of phenolic foams/halogen‐free flame retardant system

A halogen‐free flame retardant system consisting of ammonium polyphosphate (APP) as an acid source, blowing agent, pentaerythritol (PER) as a carbonific agent and zinc oxide (ZnO) as a synergistic agent, was used in this work to enhance flame retardancy of phenolic foams. ZnO was incorporated into flame retardant formulation at different concentrations to investigate the flammability of flame retardant composite phenolic foams (FRCPFs). The synergistic effects of ZnO on FRCPFs were evaluated by limited oxygen index (LOI), thermogravimetric analysis (TGA), cone calorimeter tests, and images of residues. Results showed that the flame retardant significantly increased the LOI of FRCPFs. Compared with PF, heat release rate (HRR), total heat release (THR), effective heat of combustion (EHC), production or yield of carbon monoxide (COP or COY) and Oxygen consumption (O₂C) of FRCPFs all remarkably decreased. However specific extinction area (SEA) and total smoke release (TSR) significantly increased, which agreed with the gas‐phase flame retardancy mechanism of the flame retardant system. The results indicated that FRCPFs have excellent fire‐retardant performance and less smoke release. And the bending and compression strength were decreased gradually with the increase of ZnO. The comprehensive properties of FRCPFs were better when the amount of ZnO was 1～1.5%. © 2015 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2015 , 132, 42730.     

A P/N-containing flame retardant constructed by phosphaphenanthrene,phosphonate, and triazole and its flame retardant mechanism in reducing fire hazards of epoxy resin

A P/N-containing flame retardant (PPT) constructed by phosphaphenanthrene, phosphonate, and triazole groups was successfully synthesized and used as a reactive co-curing agent for epoxy resin (EP). The curing behavior, thermal property, combustion behavior, and flame retardant mechanism of EP thermosets were comprehensively investigated. According to the analysis of DSC and TGA, PPT accelerated the crosslinking reaction and enhanced the charring ability for EP thermosets at high temperature. The results of combustion test indicated that PPT endowed epoxy thermoset with outstanding flame retardancy. When the phosphorus content was 0.71 wt%, EP/DDS/PPT-2 achieved a LOI value of 33.2% and passed V-0 rating in UL-94 test, and its peak heat release rate and total heat release were decreased by 63.7 and 30.5%, respectively, relative to EP/DDS. Moreover, the FIGRA of EP/DDS/PPT-2 was reduced from 9.7 to 3.5 kW m⁻² s⁻¹, manifesting the significantly improved fire safety of EP thermoset. The flame retardant mechanism was summarized as two parts: (a) the barrier effect of continuous phosphorus-rich char layers in condensed phase, (b) the quenching effect of phosphorous radicals and diluting effect of nonflammable gases in gaseous phase.     

Influence of fullerenes on the thermal and flame-retardant properties of polymeric materials

At present, the application of fullerene in polymer materials has become an attractive issue. Fullerene can enhance the thermal and flame-retardant properties of polymers due to its high capacity to trap free radicals. Fullerene also has good synergistic effect with inorganic metal flame retardant, intumescent flame retardant, brominated flame retardant (BFR), clay, carbon nanotubes, graphene oxide, and so on. In this review, the impact and mechanism of fullerene and its derivatives on the thermal and flame-retardant properties of polymeric materials are discussed. And the prospect of fullerene in flame-retardant polymer composites is also briefly introduced by analyzing the research progress in the recent years. © 2019 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2020 , 137, 47538.     

Synthesis and properties of a phosphate ester as curing agent in an epoxy resin system

Phosphate ester compounds display good flame retardancy effect in epoxy resin systems. In this paper, several novel phosphate esters, used as curing agents for epoxy resins, were synthesized based on P₂O₅, phosphoric acid, and different types of alcohol. The structures of phosphate esters were characterized by ³¹P nuclear magnetic resonance (³¹P NMR). Then, a series of flame retardant epoxy composites were prepared by curing the epoxy resins (E-44) with the phosphate esters. The flame retardancy and thermal degradation behaviors of flame retardant epoxy composites were investigated by cone calorimeter test (CCT) and thermogravimetric analysis (TGA), respectively. The results of CCT indicated that phosphate esters can significantly decrease heat release rate, total heat release (THR), and smoke production rate. The sample cured by butyl phosphate ester from phosphorus pentoxide, phosphoric acid and butanol showed the best flame retardant performance among all samples. The TGA results showed that phosphate esters could enhance char residues of flame retardant epoxy composites when compared with those of a composite using T31 as a curing agent at high temperature. It may be concluded that good flame retardant properties of flame retardant epoxy composites are related to the formation of a protective phosphorus-rich char layer. These phosphate esters have a good future on flame retardant epoxy composites.     

Improving the Flame Retardancy and Smoke Suppression of Poly(Lactic Acid) with a SiO2@ammonium Molybdate Core-Shell Nanotubes

Design and fabrication of SiO₂@ammonium molybdate(AM) core-shell nanotubes are important for polylactic acid (PLA), these two components form a well-defined core-shell configuration that is distinct from simple core-shell or hybrid structures. The PLA was investigated by limiting oxygen index, vertical burning test and smoke density, cone calorimeter test, SEM and TGA. The results showed that SiO₂@AM nanotube can effectively increase the flame retardancy and smoke suppression properties, and that it can apparently reduce heat release rate, total heat release and total smoke release. Furthermore, the addition of SiO₂@AM nanotube brings better mechanical properties than the sample contain SiO₂ nanotube. Here, SiO₂@AM nanotube was considered to be an effective flame retardant in PLA.     

Excellent role of Cu2O on fire safety of epoxy resin with ammonium polyphosphate based on the construction of self-intumescent flame retardant system

This work reports an effective self-intumescent flame retardant system for epoxy resin (EP) based on the remarkable synergistic effect between Cu₂O and ammonium polyphosphate (APP). The effect of Cu₂O/APP on improving EP's fire performance was evaluated by limited oxygen index (LOI), UL-94, and cone calorimeter test. The optimal mass ratio of Cu₂O: APP was shown to be 2:8. With 15 wt% total flame retardant loading, the EP with optimum Cu₂O/APP formulation reached V-0 classification and high LOI (33.5%), while the EP with APP only got NR and low LOI (26.5%). Additionally, the pHRR, total heat release, total smoke production, CO production of the EP with optimum Cu₂O/APP formulation were primarily decreased. All the improvements were ascribed to the formation of the self-intumescent char layer of EP resulted from the catalyzing effect of Cu₂O for char formation and CO to CO₂ conversion. These findings will consolidate approaches for conferring flame retardancy to flammable polymers or their blends.     

茶皂素基膨胀型阻燃剂的制备及其在涂料中的应用

采用多羟基、多羧基的活性天然产物茶皂素为原料,与聚磷酸铵和季戊四醇在一定条件下反应,制备一种聚磷酸酯类茶皂素基三位一体新型环保膨胀型阻燃剂。采用傅里叶红外分析技术对阻燃剂进行了结构表征,采用综合热分析仪对阻燃剂的热降解性能进行了研究。结果表明,茶皂素与聚磷酸铵、季戊四醇发生反应,生成聚磷酸酯类茶皂素基膨胀型阻燃剂,且该阻燃剂具有良好的热稳定性,降解热释放较小,高温残留率高,最终的质量残留率高达30.77%。将制备阻燃剂用于阻燃涂料中,并采用氧指数测试仪和锥形量热仪研究了阻燃涂料的阻燃性能和热解性能。研究表明,茶皂素基三位一体膨胀型阻燃剂能显著提高涂料的阻燃性能,阻燃涂料的氧指数值高达34.2%,耐火时间为11.1 min,且锥形量热实验中,该阻燃涂料试样的平均热释放速率（m-HRR）为36.18 kW/m2,总热释放量（THR）为5.25 kJ/m2,平均有效燃烧热（m-EHC）为5.11 kJ/kg,与含复合型阻燃剂的阻燃涂料试样相比,阻燃性能得到极大提高。该制备阻燃剂不含卤素,集三源一体,具有阻燃性能优越,相容性能良好,高效环保等优点。