Synergist flame retarding effect of ultrafine zinc borate on LDPE/IFR system

The flame retardancy of low‐density polyethylene (LDPE) treated with complex flame retardant composed of ultrafine zinc borate (UZB) and intumescent flame retardant (IFR) have been investigated by limited oxygen index (LOI), UL‐94 test, thermogravimetric analysis (TGA), cone calorimeter test, scanning electron micrograph (SEM), energy‐dispersive spectrometer (EDS), and X‐ray diffraction (XRD). The results of LOI and UL‐94 test indicate the desired flame retardancy of LDPE is obtained when the mass ratio of UZB to IFR is 4.2 : 25.8 and the complex flame retardant mass content is 30% (based on LDPE). The results of cone calorimeter show that heat release rate (HRR) peak, total heat release (THR), and mass loss of LDPE/IFR/UZB decrease substantially when compared with those of LDPE/IFR. TGA results show that the residue of LDPE/IFR/UZB increases obviously than that of LDPE/IFR when the temperature is above 600°C. SEM indicates the quality of char forming of LDPE/IFR/UZB is superior to that of LDPE/IFR. The results of EDS and XRD indicate that boron orthophosphate (BPO₄) and zinc‐contained compounds are formed in the residual char and these substances may play an important role in stabilizing the intumescent char structure and decrease the degradation speed substantially when subjected to high temperature. © 2006 Wiley Periodicals, Inc. J Appl Polym Sci 103: 3667–3674, 2007     

超细硼酸锌对LDPE/IFR体系热稳定性的影响

采用热重-差热联机分析和傅里叶变换红外光谱研究了超细硼酸锌(UZB)对膨胀型阻燃剂阻燃低密度聚乙烯的热降解过程的影响。结果表明:UZB对膨胀阻燃低密度聚乙烯体系具有明显的热稳定作用,可使体系起始热失重温度提高,并且显著增加残炭量。差热分析结果表明,UZB可进一步降低膨胀阻燃低密度聚乙烯体系热分解的放热量,降低热降解速度;红外光谱分析表明,UZB与膨胀型阻燃剂阻燃低密度聚乙烯复合体系热解残余物具有芳烃结构的类石墨炭层及含P-O-P、P-O-C、B-B的复杂炭层结构,对内部基材具有良好的高温保护作用。     

Effect of ultrafine zinc borate on the smoke suppression and toxicity reduction of a low‐density polyethylene/intumescent flame‐retardant system

The production of smoke, carbon monoxide (CO), and carbon dioxide (CO₂) were investigated with cone calorimetry testing when low‐density polyethylene (LDPE), LDPE treated with an intumescent flame retardant (IFR), and LDPE treated with an IFR and ultrafine zinc borate (UZB) combusted under irradiation. The results of the testing showed that UZB could depress smoke production and reduce the amount of CO and CO₂. The components of the pyrolytic gas and its contents were identified and measured with pyrolysis–gas chromatography/mass spectrometry (Py–GC–MS) when LDPE, LDPE/IFR, and LDPE/IFR/UZB were pyrolyzed at 400°C for 20 s. The Py–GC–MS results implied that UZB had an important influence on the components and contents of the pyrolytic gas of LDPE/IFR. UZB mechanisms of smoke suppression and toxicity reduction with respect to LDPE/IFR are proposed. © 2010 Wiley Periodicals, Inc. J Appl Polym Sci, 2010     

超细硼酸锌对LDPE/IFR体系抑烟性能的影响

用锥形量热法研究了超细硼酸锌对膨胀型阻燃低密度聚乙烯(LDPE/IFR)体系燃烧时发烟量和气体(CO、CO2)释放量的影响。结果表明:在超细硼酸锌引入LDPE/IFR体系后,烟产生速率的峰值从0.0427m2/s降低到0.0151m2/s,总烟释放量由1340.95降低为719.6,烟产生速率峰值出现的时间推后,证明了超细硼酸锌具有显著的抑烟作用,同时对LDPE/IFR体系燃烧时产生的CO和CO2也具有显著的抑制作用。     

An effective intumescent flame retardancy of LDPE induced by the combination of APP and CNCO‐HA

A char‐forming agent poly(4,6‐dichloro‐N‐hydroxyethyl?1,3,5‐triazin‐2‐amine‐1,6‐diaminohexane) (CNCO‐HA) containing triazine rings was chosen for improving the flame retardant of low density polyethylene (LDPE). The synergistic effect of CNCO‐HA and Ammonium polyphosphate (APP) on the flame retardancy and char‐forming behavior of LDPE were investigated. The limited oxygen index (LOI) and vertical burning test (UL‐94) results indicated the optimal weight ratio of APP to CNCO‐HA was 3:1, and the LOI value of composite reached 31.0% with 30% intumescent flame retardant (IFR) loading. The cone calorimeter test analysis revealed that IFR presented excellent char forming and smoke suppression ability, and resulted in the efficient decrease of combustibility parameters. The thermogravimetric analysis results demonstrated that IFR reduced the thermal degradation rate at main stage of degradation. Scanning electron microscopy observed that IFR promoted to form a compact and continuous intumescent char layer. The Laser Raman spectroscopy spectra showed that larger graphitization degree was formed to enhance the strength of char, and Fourier transform infrared results presented that P‐O‐C and P‐O‐P structures in the residue char were formed to improve shield performance of the char layer to obtain better flame retardant properties of the composite. © 2016 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2016 , 133, 43950.     

Flame retardation and thermal degradation of intumescent flame‐retarded polypropylene composites containing spirophosphoryldicyandiamide and ammonium polyphosphate

A novel halogen‐free intumescent flame retardant, spirophosphoryldicyandiamide (SPDC), was synthesized and combined with ammonium polyphosphate (APP) to produce a compound intumescent flame retardant (IFR). This material was used in polypropylene (PP) to obtain IFR‐PP systems whose flammability and thermal behavior were studied by the limiting oxygen index (LOI) test, UL‐94, thermogravimetric analysis, and cone calorimetry. In addition, the mechanical properties of the systems were investigated. The results indicated that the compound intumescent flame retardant showed both excellent flame retardancy and antidripping ability for PP when the two main components of the IFR coexisted in appropriate proportions. The optimum flame retardant formulation was SPDC:APP = 3:1, which gave an LOI value of 38.5 and a UL‐94 V‐0 rating. Moreover, the heat release rate, production of CO, smoke production rate, and mass loss rate of the IFR‐PP with the optimum formulation decreased significantly relative to those of pure PP, according to the cone calorimeter analysis. The char residues from the cone calorimetry experiments were observed by scanning electron microscopy, which showed that a homogeneous and compact intumescent char layer was formed. J. VINYL ADDIT. TECHNOL., 2010. © 2010 Society of Plastics Engineers     

Influence of the pentaerythritol phosphate melamine salt content on the combustion and thermal decomposition process of intumescent flame‐retardant ethylene–vinyl acetate copolymer composites

Pentaerythritol phosphate melamine salt (PPMS) as a single‐molecule intumescent fire retardant was synthesized and characterized. The influence of the PPMS content on the combustion and thermal decomposition processes of intumescent‐flame‐retardant (IFR) ethylene–vinyl acetate copolymer (EVA) composites was studied by limiting oxygen index (LOI) measurement, UL 94 rating testing, cone calorimetry, thermogravimetric analysis, and scanning electron microscopy. The LOI and UL 94 rating results illustrate that PPMS used in EVA improved the flame retardancy of the EVA composites. The cone calorimetry test results show that the addition of PPMS significantly decreased the heat‐release rate, total heat release, and smoke‐production rate and enhanced the residual char fire performance of the EVA composites. The IFR–EVA3 composite showed the lowest heat‐release and smoke‐production rates and the highest char residue; this means that the IFR–EVA3 composite had the best flame retardancy. The thermogravimetry results show that the IFR–EVA composites had more residual char than pure EVA; the char residue yield increased with increasing PPMS content. The analysis results for the char residue structures also illustrated that the addition of PPMS into the EVA resin helped to enhance the fire properties of the char layer and improve the flame retardancy of the EVA composites. © 2015 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2015 , 132, 42148.     

Effect of zinc borate on the fire and thermal degradation behaviors of a poly(3-hydroxybutyrate-co-4-hydroxybutyrate)-containing intumescent flame retardant

The aim of this study was to investigate the effect of zinc borate (ZnB) on the fire and thermal degradation behaviors of a poly(3-hydroxybutyrate-co-4-hydroxybutyrate) [P(3,4)HB]-containing intumescent flame retardant (IFR). The IFR system was composed of ammonium polyphosphate, pentaerythritol, and melamine. The fire properties of P(3,4)HB/IFR/ZnB blends were evaluated by limited oxygen index, Underwriters Laboratories 94, microscale combustion calorimetry (MCC), and cone calorimetry (CONE) testing. The results of MCC and CONE show that the peak heat release rate, which is an important indicator of material fire hazard, of P(3,4)HB/IFR decreased when a small amount of the IFR was substituted by ZnB. The thermal degradation behavior of the P(3,4)HB/IFR/ZnB blends were measured by thermogravimetric analysis and thermogravimetric analysis–infrared (TG–IR) spectrometry. The data of TG–IR showed that the flammable gas products of P(3,4)HB released during the thermal degradation process were greatly decreased. Scanning electron microscopy analysis revealed that more compact char residues were observed with the incorporation of ZnB. © 2012 Wiley Periodicals, Inc. J Appl Polym Sci, 2012     

Synergistic flame‐retardant effect of halloysite nanotubes on intumescent flame retardant in LDPE

Synergistic flame‐retardant effect of halloysite nanotubes (HNTs) on an intumescent flame retardant (IFR) in low‐density polyethylene (LDPE) was investigated by limited oxygen index (LOI), vertical burning test (UL‐94), thermogravimetric analysis (TGA), cone calorimeter (CC) test, and scanning electronic microscopy (SEM). The results of LOI and UL‐94 tests indicated that the addition of HNTs could dramatically increase the LOI value of LDPE/IFR in the case that the mass ratio of HNTs to IFR was 2/28 at 30 wt % of total flame retardant. Moreover, in this case the prepared samples could pass the V‐0 rating in UL‐94 tests. CC tests results showed that, for LDPE/IFR, both the heat release rate and the total heat release significantly decreased because of the incorporation of 2 wt % of HNTs. SEM observations directly approved that HNTs could promote the formation of more continuous and compact intumescent char layer in LDPE/IFR. TGA results demonstrated that the residue of LDPE/IFR containing 2 wt % of HNTs was obviously more than that of LDPE/IFR at the same total flame retardant of 30 wt % at 700°C under an air atmosphere, and its maximum decomposing rate was also lower than that of LDPE/IFR, suggesting that HNTs facilitated the charring of LDPE/IFR and its thermal stability at high temperature in this case. Both TGA and SEM results interpreted the mechanism on the synergistic effect of HNTs on IFR in LDPE, which is that the migration of HNTs to the surface during the combustion process led to the formation of a more compact barrier, resulting in the promotion of flame retardancy of LDPE/IFR. In addition, the mechanical properties of LDPE/IFR/HNTs systems were studied, the results showed that the addition of 0.5–2 wt % of HNTs could increase the tensile strength and the elongation at break of LDPE/IFR simultaneously. © 2013 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2014 , 131, 40065.     

Flame retardancy and water resistance of novel intumescent flame‐retardant oil‐filled styrene–ethylene–butadiene–styrene block copolymer/polypropylene composites

A novel halogen‐free flame‐retardant composite consisting of an intumescent flame retardant (IFR), oil‐filled styrene–ethylene–butadiene–styrene block copolymer (O‐SEBS), and polypropylene (PP) was studied. On the basis of UL‐94 ratings and limiting oxygen index (LOI) data, the IFRs consisted of a charring–foaming agent, ammonium polyphosphate, and SiO₂ showed very effective flame retardancy and good water resistance in the IFR O‐SEBS/PP composite. When the loading of IFR was only 28 wt %, the IFR–O‐SEBS/PP composite could still attain a UL‐94 V‐0 (1.6 mm) rating, and its LOI value remained at 29.8% after a water treatment at 70°C for 168 h. Thermogravimetric analysis data indicated that the IFR effectively enhanced the temperature of the main thermal degradation peak of the IFR–O‐SEBS/PP composites because of the formation of abundant char residue. The flammability parameters of the composites obtained from cone calorimetry testing demonstrated that water treatment almost did not affect the flammability behavior of the composite. The morphological structures of the char residue and fractured surfaces of the composites were not affected by the water treatment. This was attributed to a small quantity of IFR extracted from the composite. © 2013 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2014 , 131, 39575.     

Flammability of EVA/IFR (APP/PER/ZB system) and EVA/IFR/synergist (CaCO3, NG,and EG) composites

Poly(ethylene‐co‐vinyl acetate)/intumescent flame retardant (ammonium polyphosphate/pentaerythritol/zinc borate system) composites‐EVA/IFR (APP/PER/ZB system) and EVA/IFR/Synergist [CaCO₃, natural graphite, or expanded graphite (EG)] composites have been prepared by melting compounding method. The flammability, the combustion process, the quantity of the residual chars, the morphology of the residual chars, and the thermal stability of the chars have been investigated by cone calorimeter, scanning electron microscopy and thermo gravimetric analysis. The results indicate that heat release rate (HRR), total heat released, and total smoke release (TSR) of EVA/IFR (IFR 30 phr) composite decrease to about 67.1, 78.2, and 64% of that of pure EVA, respectively. HRR, THR, and TSR of EVA/IFR/EG (IFR 9 phr, EG 1phr) composite decrease to about 62.1, 76.2, and 44% of that of pure EVA, respectively. The quantity, the thermal stability of residual chars and the char structure are discussed to find the reasons of the phenomenon above. It has been found that the flame retardant of EVA vulcanizates is improved and the fire jeopardizing is dramatically reduced due to the addition of IFR and synergist, which can give some advice to design formulations for practical applications as cable. © 2012 Wiley Periodicals, Inc. J Appl Polym Sci, 2012     

Flame Retardancy and Thermal Performance of Polypropylene Treated With the Intumescent Flame Retardant,Piperazine Spirocyclic Phosphoramidate

Piperazine spirocyclic phosphoramidate (PSP), a novel halogen‐free intumescent flame retardant, was synthesized and used to improve the flame retardancy and dripping resistance of polypropylene (PP) combined with ammonium polyphosphate (APP) and a triazine polymer charring‐foaming agent (CFA). The optimum flame‐retardant formulation was PSP:APP:CFA = 3:6:2 (weight ratio). The flammability and thermal behavior of the (intumescent flame‐retardant)‐PP (IFR‐PP) were investigated via limiting oxygen index (LOI), vertical burning tests (UL‐94), thermogravimetric analysis, and cone calorimetry (CONE). The results indicated that the IFR‐PP had both excellent flame retardancy and anti‐dripping ability. The optimum flame‐retardant formulation gave an LOI value of 39.8 and a UL‐94 V‐0 rating to PP. Moreover, both the heat release rate and the total heat release of the IFR‐PP with the optimum formulation decreased significantly relative to those of pure PP, according to the cone calorimeter analyses. The residues of IFR‐PP obtained after CONE tests were observed by scanning electron microscopy, and it was found that the char yield was directly related to the flame retardancy and anti‐dripping behavior of the treated PP. J. VINYL ADDIT. TECHNOL., 20:10–15, 2014. © 2014 Society of Plastics Engineers     

Experimental study on polystyrene with intumescent flame retardants from different scale experiments

In this study, the fire performance and toxicity of intumescent flame retardant (IFR) polystyrene composites were investigated experimentally. Ammonium polyphosphate, pentaerythritol, and melamine were selected as IFR. The flammability of the polystyrene (PS) composites was evaluated by microscale combustion calorimetry and cone calorimetry and in the ISO Room. The results suggested that the thermal stability and the peak heat release rate of PS composites decreased with the increasing content of IFR. In the cone calorimeter and ISO 9705 testing, the carbon monoxide yield of PS composites also decreased markedly with the addition of IFR. Scanning electron microscope images show that the char from cone calorimetry testing was more compact and smoother than that from the ISO 9705 testing. The comparison between bench‐ and full‐scale tests demonstrated that the flammability and the toxicity of PS composites are decreased markedly due to the incorporation of the flame retardant, but considerable differences exist. Copyright © 2014 John Wiley & Sons, Ltd.     

Effect of a novel phosphorus‐containing compound on the flame retardancy and thermal degradation of intumescent flame retardant polypropylene

A novel flame retardant, tetra(5,5‐dimethyl‐1,3‐ dioxaphosphorinanyl‐2‐oxy) neopentane (DOPNP), was synthesized successfully, and its structure was characterized by FT‐IR, ¹H NMR, and ³¹P NMR. The thermogravimetric analysis (TGA) results demonstrate that DOPNP showed a good char‐forming ability. Its initial decomposition temperature was 236.4°C based on 1% mass loss, and its char residue was 41.2 wt % at 600°C, and 22.9 wt % at 800°C, respectively. The flame retardancy and thermal degradation behavior of novel intumescent flame‐retardant polypropylene (IFR‐PP) composites containing DOPNP were investigated using limiting oxygen index (LOI), UL‐94 test, TGA, cone calorimeter (CONE) test, and scanning electron microscopy (SEM). The results demonstrate that DOPNP effectively raised LOI value of IFR‐PP. When the loading of IFR was 30 wt %, LOI of IFR‐PP reached 31.3%, and it passed UL‐94 V‐0. TGA results show that DOPNP made the thermal decomposition of IFR‐PP take place in advance; reduced the thermal decomposition rate and raised the residual char amount. CONE results show that DOPNP could effectively decrease the heat release rate peak of IFR‐PP. A continuous and compact char layer observed from the SEM further proved the flame retardance. © 2011 Wiley Periodicals, Inc. J Appl Polym Sci, 2011.     

Application of a novel halogen‐free intumescent flame retardant for acrylonitrile‐butadiene‐styrene

A novel intumescent flame retardant (IFR), containing ammonium polyphosphate (APP) and poly(tetramethylene terephthalamide) (PA4T), was prepared to flame‐retard acrylonitrile‐butadiene‐styrene (ABS). The flame retardation of the IFR/ABS composite was characterized by limiting oxygen index (LOI) and UL‐94 test. Thermogravimetric analysis (TGA) and TGA coupled with Fourier transform infrared spectroscopy (TG‐FTIR) were carried out to study the thermal degradation behavior of the composite and look for the mechanism of the flame‐retarded action. The morphology of the char obtained after combustion of the composite was studied by scanning electron microscopy (SEM). It has been found the intumescent flame retardant showed good flame retardancy, with the LOI value of the PA4T/APP/ABS (7.5/22.5/70) system increasing from 18.5 to 30% and passing UL‐94 V‐1 rating. Meanwhile, the TGA and TG‐FTIR work indicated that PA4T could be effective as a carbonization agent and there was some reaction between PA4T and APP, leading to some crosslinked and high temperature stable material formed, which probably effectively promoted the flame retardancy of ABS. Moreover, it was revealed that uniform and compact intumescent char layer was formed after combustion of the intumescent flame‐retarded ABS composite. © 2011 Wiley Periodicals, Inc. J Appl Polym Sci, 2012     

Synthesis of amino trimethylene phosphonic acid melamine salt and its application in flame‐retarded polypropylene

Amino trimethylene phosphonic acid melamine salt (MATMP) was synthesized and used as acid source and blowing agent in intumescent flame‐retarded polypropylene (PP); its compositions were characterized by Fourier transform infrared spectroscopy and X‐ray powder diffraction. An intumescent flame retardant (IFR) system composed of MATMP, pentaerythritol (PER), and PP was tested by limiting oxygen index (LOI), UL‐94, cone calorimeter tests, and thermogravimetric analysis and compared with an ammonium polyphosphate (APP)/PER system. The results showed that MATMP had better water resistance than APP, the LOI value of PP/MATMP/PER composite can reach 30.3%, and a UL‐94 V‐0 rating can be reached at 25 wt % IFR loading. The amount of residual char of IFR MATMP/PER was 20.3 and 9.5 wt % at 400 and 600 °C, respectively. A thermooxidative degradation route and a possible flame‐retardant mechanism of IFR were proposed according to the analysis of evolved gases and residual chars. © 2018 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2018 , 135, 46274.     

Synergistic effect between aluminum hypophosphite and a new intumescent flame retardant system in poly(lactic acid)

A hyperbranched charring agent (CT) was synthesized by triglycidyl isocyanurate and diethylenetriamine in water, and a new intumescent flame retardant (IFR) system was formed by ammonium polyphosphate (APP) and CT. The different formula and synergistic system between IFR and aluminum hypophosphite (AHP) have been studied through limit oxygen index (LOI), UL‐94, cone calorimetry test and TGA. It was found that the LOI for poly(lactic acid) (PLA) with 30 APP/CT (4:1) and 20 wt % IFR/AHP (3:1) were 41.2% and 43.5%, respectively, and the both could achieve UL‐94V‐0 rating with no melt dripping. The heat release rate (HRR), maximum HRR value and average mass loss rate of PLA could be dramatically decreased by combination of IFR and AHP while the thermal stability was greatly enhanced. The study of morphology and structure of char illustrated that more intumescent and compact char layer with good intensity was formed during the degradation of IFR/AHP, which resulting to better flame retardancy and anti‐dripping than IFR or AHP alone. © 2018 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2018 , 135, 46359.     

Flammability,thermal stability,and mechanical properties of ethylene-propylene-diene monomer/polypropylene composites filled with intumescent flame retardant and inorganic synergists

Three kinds of inorganic particles, zinc borate (ZB), organic montmorillonite (OMMT), and expanded graphite (EG) as synergistic flame retardants, are incorporated into ethylene-propylene-diene monomer/polypropylene (EPDM/PP) composites filled with intumescent flame retardants (IFR). The effect of three synergistic flame retardants on the combustion, thermal stability, and mechanical properties of the EPDM/PP/IFR composites are investigated by limiting oxygen index (LOI), UL-94 test, cone calorimeter test (CCT), thermogravimetric analysis (TGA), scanning electron microscopy, mechanical property testing, and dynamic mechanical analysis (DMA). The results from LOI, UL-94, and CCT show that the synergistic effect of IFR with ZB and EG is better than IFR with OMMT in the flame retardant EPDM/PP/IFR composites. The TGA results indicate that the thermal stability and char residues of the composites is improved with the addition of inorganic particles, which is attributed to the formation of dense char layers to isolate heat flow. DMA results including storage modulus (G'), loss modulus (G"), and loss factor (tan δ) suggest that the composites with inorganic particles exhibit more rubber-filler interaction, which limits the movement of the rubber chains.     

有机-金属杂化化合物阻燃聚丙烯的研究

将有机-金属杂化三嗪化合物（SCTCFA-ZnO）与聚磷酸铵（APP）复配制备了膨胀型阻燃剂（IFR）,通过极限氧指数测试、垂直燃烧测试、锥形量热分析、热失重分析和扫描电子显微镜分析等表征方法研究了SCTCFA-ZnO/APP的协同作用对PP复合材料阻燃性能的影响。结果表明,APP与SCTCFA-ZnO复配可以有提高PP材料的阻燃性能,当IFR的添加量为25 %（质量分数,下同）,且APP/SCTCFA-ZnO的质量比为2/1时,复合材料的极限氧指数最高,达到31.1 %,达到UL 94 V-0级;IFR可提高复合体系的温热稳定性,阻燃复合材料燃烧后会形成一层致密、连续的炭层,从而起到良好的阻燃效果。     

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