Halogen‐free flame‐retardant rigid polyurethane foams: Effect of alumina trihydrate and triphenylphosphate on the properties of polyurethane foams

Rigid polyurethane foam (PUF) filled with mixture of alumina trihydrate (ATH) and triphenyl phosphate (TPP) as fire retardant additive was prepared with water as a blowing agent. In this study, the ATH content was varied from 10 to 100 parts per hundred polyol by weight (php), and TPP was used at a higher loading of ATH (75 and 100 php) in a ratio of 1 : 5 to enhance the processing during PUF preparation. The effects of ATH on properties such as density, compressive strength, morphological, thermal conductivity, thermal stability, flame‐retardant (FR) behavior, and smoke characteristics were studied. The density and compressive strength of the ATH‐filled PUF decreased initially and then increased with further increase in ATH content. There was no significant change in the thermal stability with increasing ATH loading. We determined the FR properties of these foam samples by measuring the limiting oxygen index (LOI), smoke density, rate of burning, and char yield. The addition of ATH with TPP to PUF significantly decreased the flame‐spread rate and increased LOI. The addition of TPP resulted in easy processing and also improved FR characteristics of the foam. © 2010 Wiley Periodicals, Inc. J Appl Polym Sci, 2010     

Synthesis of a deoxybenzoin derivative and its use as a flame retardant in poly(trimethylene terephthalate)

A Friedel–Crafts acylation reaction was used to synthesize a deoxybenzoin derivative named bis[2,6‐dimethyl‐4‐(2‐phenyl acetyl)phenyl]phenyl phosphonate (BDPP), which could be used as a flame‐retardant additive in poly(trimethylene terephthalate) (PTT) resin. The limited oxygen index and cone calorimetry tests indicated that the introduction of 5 wt % BDPP significantly improved the flame‐retardant properties of PTT through a synergistic char‐formation mechanism in the condensed phase and a flame‐inhibition mechanism in the gas phase. The PTT–BDPP blend also demonstrated an evident reduction in the melt viscosity but a superior melt stability in comparison to the neat PTT. © 2017 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2018 , 135, 45904.     

Effect of charring agent THEIC on flame retardant properties of polypropylene

Tris(2‐hydroxyethyl) isocyanurate (THEIC) was used as charring agent and combined with ammonium polyphosphate (APP) to form an intumescent flame retardant (IFR) for polypropylene (PP). The flame retardancy and combustion performance of PP/IFR composite was tested by limiting oxygen index (LOI), UL‐94 vertical burning test and cone calorimeter. The results showed that PP/IFR composite had highest LOI of 34.8 and obtained V‐0 rating when 30 wt % IFR was loaded and mass ratio APP/THEIC was 2 : 1. The peak heat release (PHRR) and total heat release (THR) values of PP composite containing FRs were remarkably reduced compared with that of pure PP. However, water resistant test demonstrated the PP/IFR composite had poor flame retardant durability, both the LOI value and UL‐94 V‐rating decreased when PP/IFR composite was soaked in water at 70°C after 36 h. The degradation process and the char morphology of IFR and PP/IFR composite were investigated by TGA and SEM images. The possible reaction path between APP and THEIC in the swollen process was proposed. © 2014 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2015 , 132, 41214.     

Thermal and fire behavior of isophorone diisocyanate based polyurethane foams containing conventional flame retardants

This work reports on the fire behavior of isophorone diisocyanate‐based polyurethane foams containing different conventional flame retardants (FRs) such as melamine, ammonium polyphosphate, aluminum hydroxide, expandable graphite, and their combinations. The foams were obtained in a laboratory scale and characterized in terms of their morphology, density, thermal stability, and fire behavior. According to atomic force microscopy, the incorporation of FRs decreased the phase separated domain size. The cellular structure of the foams was examined qualitatively by scanning electron microscopy while the quantitative analysis of the surrounding skin was performed by optical microscopy and Image J. The FR containing foams showed more and smaller cells. The thermogravimetric analysis showed that the FRs had no influence in the initial degradation temperature of the foams. However, the obtained residue values were higher than the theoretical ones, indicating that there was some type of interaction between the FRs and the foams. The fire behavior of polyurethane foams was studied by the cone calorimeter and the data showed that the introduction of expandable graphite and combinations of ammonium polyphosphate/melamine to the reference foam gave rise to a significant reduction in the total heat release. © 2017 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2018 , 135, 45944.     

Fire retardance and smoke suppression of polypropylene with a macromolecular intumescent flame retardant containing caged bicyclic phosphate and piperazine

A macromolecular intumescent flame retardant (FR) named PPPAP was designed and synthesized with phosphorus chloride (the acid source), 2,6,7-trioxa-l-phosphabicyclo[2.2.2]-octane-4-methanol (the charring agent), and anhydrous piperazine (the blowing agent). Then, it was used to prepare an intumescent flame-retardant polypropylene (FR-PP). The thermal stability, flame retardancy, and fire performance of the FR-PPs were investigated. The results show that the initial decomposition temperature and char residue at 700 °C of PPPAP were 260.8 °C and 31.8%, respectively. The limiting oxygen index (LOI) value of polypropylene (PP) was enhanced with increasing PPPAP content. With the addition of 40 wt % PPPAP, the LOI value of FR-PP was 29%, and it passed the vertical burning UL-94 V-0 rating. The cone calorimetry results indicate that not only the peak heat-release rate but also the total smoke production of PP significantly decreased to 65.7 and 79.5%, respectively, with the incorporation of only 20 wt % PPPAP. The FR mechanism suggested that PPPAP played a part in both the gas and condensed phases, and the formation of the intumescent char layer during combustion was the dominant FR mechanism. © 2019 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2019 , 136, 47593.     

Green synthesis and characterization of phosphorus flame retardant crosslinking agents for epoxy resins

The flame‐retardant efficacy of phosphorus‐containing reactive amine hardeners for epoxy resins is well‐known; however their synthesis often applies hazardous, objectionable reagents. The aim of this work is to develop an effective synthesis method for the preparation of P‐containing amines, which can act as flame‐retardant crosslinking agent in epoxy resins. The syntheses and testing of an aliphatic and two aromatic amines are described: curing properties, glass transition temperature, thermal stability, and flame‐retardant performance of the amines are studied. On the basis of these results, the scaling‐up and the optimization of the synthesis of the phosphorus‐containing aliphatic amine hardener in ReactIR? in situ FTIR apparatus is discussed. © 2013 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2014 , 131, 40105.     

Morphology,thermal, and mechanical properties of flame‐retardant silicone rubber/montmorillonite nanocomposites

Flame‐retardant methyl vinyl silicone rubber (MVMQ)/montmorillonite nanocomposites were prepared by solution intercalation method, using magnesium hydroxide (MH) and red phosphorus (RP) as synergistic flame‐retardant additives, and aero silica (SiO₂) as synergistic reinforcement filler. The morphologies of the flame‐retardant MVMQ/montmorillonite nanocomposites were characterized by environmental scanning electron microscopy (ESEM), and the interlayer spacings were determined by small‐angle X‐ray scattering (SAXS). In addition to mechanical measurements and limited oxygen index (LOI) test, thermal properties were tested by thermogravimetric analysis (TGA). The decomposition temperature of the nanocomposite that contained 1 wt % montmorillonite can be higher (129°C) than that of MVMQ as basal polymer matrix when 5% weight loss was selected as measuring point. This kind of silicone rubber nanocomposite is a promising flame‐retardant polymeric material. © 2006 Wiley Periodicals, Inc. J Appl Polym Sci 99: 3275–3280, 2006     

Photopolymerization and thermal behavior of phosphate diacrylate and triacrylate used as reactive‐type flame‐retardant monomers in ultraviolet‐curable resins

Tri(acryloyloxyethyl)phosphate (TAEP) and di(acryloyloxyethyl)ethyl phosphate (DAEEP) were used as reactive‐type flame‐retardant monomers along with commercial epoxy acrylate and polyurethane acrylate oligomers in ultraviolet (UV)‐curable resins. The concentrations of the monomers were varied from 17 to 50 wt %. The addition of the monomers greatly reduced the viscosity of the oligomers and increased the photopolymerization rates of the resins. The flame retardancy and thermal degradation behavior of the UV‐cured films were investigated with the limiting oxygen index (LOI) and thermogravimetric analysis. The results showed that the thermal stability at high temperatures greater than 400°C and the LOI values of the UV‐cured resins, especially those containing epoxy acrylate, were largely improved by the addition of the monomers. The dynamic mechanical thermal properties of the UV‐cured films were also measured. The results showed that the crosslink density increased along with the concentrations of the monomers. However, the glass‐transition temperature decreased with an increasing concentration of DAEEP because of the reduction in the rigidity of the cured films, whereas the glass‐transition temperature increased with the concentration of TAEP because of the higher crosslink density of the cured films. © 2005 Wiley Periodicals, Inc. J Appl Polym Sci 97: 185–194, 2005     

Synthesis of a novel phosphorus‐containing dicyclopentadiene novolac hardener and its cured epoxy resin with improved thermal stability and flame retardancy

A novel phosphorus‐containing dicyclopentadiene novolac (DCPD‐DOPO) curing agent for epoxy resins, was prepared from 9,10‐dihydro‐oxa‐10‐phosphaphenanthrene‐10‐oxide (DOPO) and n‐butylated dicyclopentadiene phenolic resin (DCPD‐E). The chemical structure of the obtained DCPD‐DOPO was characterized with FTIR, ¹H NMR and ³¹P NMR, and its molecular weight was determined by gel permeation chromatography. The flame retardancy and thermal properties of diglycidyl ether bisphenol A (DGEBA) epoxy resin cured with DCPD‐DOPO or the mixture of DCPD‐DOPO and bisphenol A‐formaldehyde Novolac resin 720 (NPEH720) were studied by limiting oxygen index (LOI), UL 94 vertical test and cone calorimeter (CCT), and differential scanning calorimetry (DSC) and thermogravimetric analysis (TGA), respectively. It is found that the DCPD‐DOPO cured epoxy resin possess a LOI value of 31.6% and achieves the UL 94 V‐0 rating, while its glass transition temperature (T_g) is a bit lower (133 °C). The T_g of epoxy resin cured by the mixture of DCPD‐DOPO and NPEH720 increases to 137 °C or above, and the UL 94 V‐0 rating can still be maintained although the LOI decreases slightly. The CCT test results demonstrated that the peak heat release rate and total heat release of the epoxy resin cured by the mixture of DCPD‐DOPO and NPEH720 decrease significantly compared with the values of the epoxy resin cured by NPEH720. Moreover, the curing reaction kinetics of the epoxy resin cured by DCPD‐DOPO, NPEH720 or their mixture was studied by DSC. © 2016 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2017 , 134, 44599.     

Synergistic flame retardant effect of piperazine salt and ammonium polyphosphate as intumescent flame retardant system for polypropylene

Amino trimethylene phosphonic acid piperazine (ATPIP) salt, as a novel charring agent, is prepared via a simple ionic reaction in distilled water using amino trimethylene phosphate (ATMP) and piperazine as raw materials. The synergistic flame retardant effect of ATPIP and ammonium polyphosphate (APP) as an intumescent flame retardant (IFR) is investigated by various characterization and testing methods. The results show that the polypropylene (PP)/modified APP with piperazine (MAPP)/ATPIP ternary blend passes UL-94 V-0 rating and achieve a limiting oxygen index (LOI) of 30% at a loading level of 25 wt% IFR (MAPP:ATPIP = 3:1). Meanwhile, the total smoke production (TSP) value of IFR-PP samples is 3.3 m², which decreases by 93.2% compared with that of pure PP, exhibiting excellent smoke suppression performance. Besides, the analysis of gaseous pyrolysis products and char residue indicates that the IFR-PP samples show a synergistic flame-retardant mechanism including the gas phase and the condensed phase.     

Expandable graphite encapsulated by magnesium hydroxide nanosheets as an intumescent flame retardant for rigid polyurethane foams

Encapsulation of expandable graphite (EG) particles by organic or inorganic shells has been proved to efficiently enhance the expandability of EG, and thus to improve the flame‐retardant efficiency of EG. In this study, magnesium hydroxide (MH) nanosheets were utilized to fabricate core–shell EG@MH flame‐retardant particles through a heterocoagulation method. It was observed that after the encapsulation by MH nanosheets, the edges of the char residue of the EG layer were sealed after combustion, which contributed to the enhancement of expandability. The expansion volume of EG@MH increased dramatically to 456 mL/g, in contrast to 338 mL/g for pure EG. By incorporating 11.5 wt % of flame‐retardant particles, polyurethane foam containing EG@MH (here PU‐EG@MH) displayed excellent flame retardancy. Compared with the physically mixed sample, PU‐EG+MH, the limiting oxygen index value for the PU‐EG@MH sample increased from 29.8% to 32.6%. Furthermore, the shell of MH nanosheets was beneficial for improving the interfacial adherence between EG and the rigid polyurethane foam (RPUF) matrix, due to the reaction between isocyanate functional groups and MH. The cell structure and storage modulus of PU‐EG@MH were improved. In other words, the shell of MH nanosheets successfully improved the flame‐retardant efficiency and enhanced the interface adhesion between EG and the matrix. © 2018 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2018 , 135, 46749.     

Melamine poly(metal phosphates) as flame retardant in epoxy resin: Performance,modes of action,and synergy

Melamine poly(metal phosphates) (MPMeP) are halogen‐free flame retardants commercialized under the brand name Safire. Melamine poly(aluminum phosphate) (MPAlP), melamine poly(zinc phosphate) (MPZnP), and melamine poly(magnesium phosphate) (MPMgP) were compared in an epoxy resin (EP). The thermal decomposition, flammability, burning behavior, and glass transition temperature were investigated using thermogravimetric analysis, pyrolysis combustion flow calorimeter, UL 94 testing, cone calorimeter, and differential scanning calorimetry. While the materials exhibited similarities in their pyrolysis, EP + MPZnP and EP + MPMgP showed better fire behavior than EP + MPAlP due to superior protective properties of the fire residues. Maintaining the 20 wt % loading, MPZnP was combined with various other flame retardants. A synergistic effect was evident for melamine polyphosphate (MPP), boehmite, and a derivative of 6H‐Dibenzo[c,e][1,2]oxaphosphinine‐6‐oxide. The best overall performance was observed for EP + (MPZnP + MPP) because of the best protection effectiveness of the fire residue. EP + (MPZnP + MPP) achieved V1/V0 in UL 94, and an 80% reduction in the peak heat release rate. This study evaluates the efficiency of MPMeP in EP, alone and in combination with other flame retardants. MPMeP is a suitable flame retardant for epoxy resin, depending on its kind and synergists. © 2016 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2016 , 133, 43549.     

A DOPO-base Schiff derivative used as a flame retardant for polystyrene

A novel 9,10-dihydro-9-oxa-10-phosphaphenanthrene-10-oxide (DOPO)-based Schiff base derivative, 6,6′-(1,4-phenylenebis (((3-hydroxyphenyl)amino) methylene)) bis (dibenzo [c,e] [1,2] oxaphosphinine 6-oxide) (SD), was synthesized and applied to polystyrene. The structure of terephthalaldehyde dihydroxymethane benzene and SD are characterized by Fourier-transform infrared (FTIR) spectroscopy, ¹H-nuclear magnetic resonance spectroscopy, and elemental analysis. The results of thermogravimetric analysis tests show that the residue of the SD/PS composites increased from 0.21 to 7.09% with the increase of SD content, indicated that the thermal stability of the SD/PS composites was significantly improved. The introduction of SD also efficiently ameliorated the flame-retardant property of SD/PS composites with limiting oxygen index increased by 33.15%, rated UL-94 vertical burning test V-0 rating, lower peak heat release rate, and total heat release. The mechanism of SD/PS composite was explored by scanning electron microscopy images and FTIR spectra of residue of SD/PS composites after calcination by muffle furnace. These tests prove that SD can be used as an effective polystyrene (PS) flame retardant.     

Preparation and properties of transparent copolymers based on cyclotriphosphazene and styrene as potential flame‐retardant optical resins

Transparent copolymers composed of hexa(allyl 4‐hydroxybenzoate) cyclotriphosphazene (compound 1 ) and styrene as potential halogen‐free, flame‐retardant optical resins were prepared by radical copolymerization. The thermal performances of the cured resins were studied with thermogravimetric analysis; the decomposition mechanism of the copolymers was investigated with integrated thermogravimetry–Fourier transform infrared analysis. Compared with conventional polystyrene, the synthesized copolymers exhibited a higher refractive index and a higher thermal stability both under nitrogen and air atmospheres at elevated temperature, and the visible‐light transmittance of the copolymers decreased slightly. With increasing ratio of compound 1 to styrene in the copolymers, the onset decomposition temperature and the char yield both increased gradually. © 2011 Wiley Periodicals, Inc. J Appl Polym Sci, 2011     

The flame retardant and thermal performances of polypropylene with a novel intumescent flame retardant

A novel mono-component intumescent flame retardant(m-IFR), called poly-(spirocyclic pentaerythritol bisphosphonate-1,3,5-triazine-O-bicyclic pentaerythritol phosphate) (PSTBP) was synthesized and characterized. PSTBP was used in polypropylene (PP) to obtain PP/PSTBP mixture whose flame retardancy, thermostability, and water resistance were studied by limiting oxygen index (LOI), vertical burning test (UL-94 V) and thermogravimetric analysis (TGA). In addition, flame-retardant mechanism of the PSTBP was investigated. The results showed that the residue of PSTBP reached 34.58% at 800°C and the volume of the PSTBP increased by dozens of times. When the content of PSTBP was 30.0 wt%, the PP/PSTBP mixture could achieve an LOI value of 32.5% and an UL-94 V-0 rating. Compared with PP/APP/PER system, PP/PSTBP mixture showed better water resistance. The TGA and Fourier transform infrared spectroscopy (FTIR) results showed that PSTBP could generate free radicals and capture the free radicals of the thermal decomposition of PP, and form a dense, strong, and thick intumescent char on the substrate, thus effectively retard the degradation and combustion of PP.     

Synthesis of a novel flame retardant containing phosphazene and triazine groups and its enhanced charring effect in poly(lactic acid) resin

A novel flame retardant heax‐[N,N′,N″‐tris‐(2‐amino‐ethyl)‐[1,3,5] triazine‐2,4,6‐triamine] cyclotriphosphazene (HTTCP) containing phosphazene and triazine groups was synthesized and characterized by Fourier transform infrared spectroscopy (FTIR), solid‐state ¹H and ¹³C nuclear magnetic resonance (NMR) spectroscopy. HTTCP was applied to PLA matrix. The results of thermal gravimetric analysis (TGA), the limited oxygen index (LOI), and cone calorimeter test indicated that the HTTCP enhanced the thermal stability and flame retardant properties of PLA. When the mass fraction of HTTCP was 25 wt %, the PLA composite acquired a LOI value of 25.2% and the lower pk‐HRR at 290 kW/m². The excellent flame retardancy of HTTCP was attributed to the group synergistic effect between phosphazene and triazine groups. However, when combined HTTCP with APP (the total amount remaining 25 wt %, the ratio of HTTP to APP are 1:1 and 1:2), high values of LOI (over 40%) and UL94 V‐0 rating without dripping reached simultaneously. Meanwhile, the heat release rate, total heat release and mass loss rate were all decreased dramatically. Scanning electron microscopy (SEM) demonstrated that HTTCP/APP system benefited to the formation of more intumescent, dense, compact char layer on the materials surface which could effectively prevent the underlying material from degradation during burning. © 2016 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2017 , 134, 44660.     

Intumescent foams—A novel flame retardant system for flexible polyurethane foams

A combination of intumescent components was evaluated as a novel flame retardant system in a flexible polyurethane foam, and the incorporation of these components gave rise to a significant enhancement of the flame retardant properties of the foam. The heat release rate was lowered at an early stage as well as throughout the fire, the total heat production was decreased and the time to ignition was prolonged. Mechanical measurements of the foam revealed enhanced properties in terms of stiffness accompanied by a large decrease in elongation at break as compared with a reference foam. © 2008 Wiley Periodicals, Inc. J Appl Polym Sci, 2008     

Halogen Free flame retardant rigid polyurethane foam with a novel phosphorus−nitrogen intumescent flame retardant

A novel phosphorous‐nitrogen containing intumescent flame retardant, toluidine spirocyclic pentaerythritol bisphosphonate (TSPB), was synthesized and characterized by Fourier transform infrared spectroscopy (FTIR), nuclear magnetic resonance (NMR). Flame retardant rigid polyurethane foams (TSPB‐RPUF) were prepared by using TSPB. The flame retardancy of TSPB on rigid polyurethane foams (RPUF) was investigated by the limiting oxygen index (LOI), vertical burning test, thermogravimetric analysis (TGA), scanning electron microscopy (SEM) and FTIR. The results showed TSPB exhibited better compatibility with RPUF and lesser negative influence on the mechanical properties of TSPB‐RPUF. When the content of TSPB was 30 pph, the LOI of TSPB‐RPUF could reach 26.5%, and a UL‐94 V‐0 rating was achieved. Furthermore, the TSPB‐RPUF exhibited an outstanding water resistance that it could still obtain a V‐0 rating after water soaking. TGA showed the charring ability of RPUF was relatively poor, However, the residual weight of TSPB‐RPUF was improved greatly. SEM and FTIR indicated the intumescent chars formed from TSPB‐RPUF were compact and smooth, which was a critical factor for protecting the substrate material from burning. © 2013 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2014 , 131, 39581.     

Fire‐retardant copolymer of acrylonitrile with O,O‐diethyl‐O‐allyl thiophosphate

A novel halogen‐free flame retardant, O,O‐diethyl‐O‐allyl thiophosphate (DATP), which simultaneously contained phosphorus and sulfur, was synthesized through a simple method. The structure of DATP was characterized by Fourier transform infrared spectroscopy, ¹H‐NMR, and mass spectroscopy. The flame‐retardant copolymer was obtained by the free‐radical copolymerization of DATP with acrylonitrile. The flammability and thermal degradation characteristics of the copolymer were assayed by limiting oxygen index measurement, thermogravimetric analysis, and differential scanning calorimetry. The results show that the incorporation of a small percentage of DATP into the copolymer had a significant effect on the retarding combustion of the copolymer, with the limiting oxygen index of the copolymer reaching 28.5% and the char yield being 68.63 wt % at 554°C. © 2009 Wiley Periodicals, Inc. J Appl Polym Sci, 2010     

Effects of inorganic fillers on the flame‐retardant and mechanical properties of rigid polyurethane foams

Rigid polyurethane foam (RPUF) composites filled with expandable graphite (EG), hollow glass microspheres (HGM), and glass fibers (GF) have been synthesized and characterized by limiting oxygen index, radiation ignition, compressing and torsion testing, and scanning electron microscopy. The results indicate HGM and GF benefit to the mechanical properties, while EG is good for flame retardancy. Proper ingredient of additive can lead to good flame retardancy and mechanical properties of the RPUF. © 2013 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2014 , 131, 40253.