Intumescent Flame Retardant System Research Articles

Study on flame retardant and smoke suppression of EPDM by sepiolite expansion flame retardant system

AbstractA large amount of smoke will be produced during the combustion of ethylene propylene diene monomer(EPDM), which seriously endangers the environment and personal safety. In this study, K‐SEP was obtained by modifying sepiolite with KH550, and two bio‐based flame retardant and smoke suppression systems AEGS and PEGS were prepared by combining ammonium polyphosphate intumescent flame retardant system (AEG) and piperazine pyrophosphate intumescent flame retardant system (PEG), respectively. The flame retardant and smoke suppression properties of AEGS and PEGS on EPDM matrix composites were investigated. The experimental results show that the LOI values of EPDM/AEGS3 and EPDM/PEGS3 composites with 3 phr K‐SEP are 8.1% and 5.5% higher than those of the blank samples without sepiolite. TSP decreased by 26.3% and 14.3% respectively, which proved that sepiolite has important research value in the field of flame retardant and smoke suppression of polymer materials.

Double cross-linked biomass aerogels with enhanced mechanical strength and flame retardancy for construction thermal insulation

Biomass aerogels are expected to be a popular material in construction field due to their sustainability, eco-friendliness and excellent thermal insulation properties. In this paper, high modulus biomass aerogels based on the principle of double cross-linking of physics and chemistry were synthesized by freeze-drying technique using gelatin, sodium carboxymethyl cellulose, glutaraldehyde, phytic acid and diatomite as raw materials. The presence of a double cross-linked network structure endowed the prepared aerogels with a low thermal conductivity (0.021–0.029 W·m−1·k−1). The density of only 0.0865 g·cm−3 biomass aerogel exhibited an extrastrong compression modulus of 31.5 MPa, which was superior to common biomass aerogels. Biomass intumescent flame retardant system composed of sodium carboxymethyl cellulose (carbon source), gelatin (gas source) and phytic acid (acid source) was used in combination with diatomite to enhance flame retardancy (limit oxygen index value up to 36.5 %, UL-94 V-0 rating and total smoke production reduced from 0.31 m2 to 0.18 m2) and thermal stability (the residue up to 48.91 %). Remarkably, the modified aerogel showed incredible hydrophobicity (hydrophobic angle of 137°). In summary, the results indicated this study proposed a novel green idea for the preparation of construction thermal insulation materials with a combination of high modulus, flame retardancy and hydrophobicity.

Investigation of MXene@APP/FDS/AgNPs@EG system for preparing multifunctional thermoplastic polyurethane composites with flame retardancy and electromagnetic shielding performance

In order to comply with the requirement of flame retardancy and electromagnetic interference (EMI) shielding for encapsulant applied to electronic devices, multifunctional thermoplastic polyurethane (TPU) composites are prepared with the construction of an intumescent flame retardant (IFR) system comprising internal conductive network. In this work, ammonium polyphosphate wrapped with MXene (MXene@APP) is attained by microencapsulation, and expandible graphite decorated with Ag nanoparticles (AgNPs@EG) is prepared by the reducibility of silk sericin. The IFR system with conductivity is established by the introduction of MXene@APP, AgNPs@EG and furfural-derived Schiff base (FDS). The as-prepared TPU/MXene@APP/FDS/AgNPs@EG composites are able to attain significant elevation in flame retardancy, exhibiting V-0 rating and a LOI value of 33.1 %. Furthermore, TPU composites are integrated with warp-knitted metal mesh (WMM) to fabricate TPU@WMM coated fabric, displaying strengthened electromagnetic interference (EMI) shielding effectiveness (SE) of 37.53 dB within X band. This work provides a potential method for application in encapsulant with flame retardancy and electromagnetic protection.

The Recyclability of Fire-Retarded Biobased Polyamide 11 (PA11) Composites Reinforced with Basalt Fibers (BFs): The Influence of Reprocessing on Structure, Properties, and Fire Behavior.

The growing requirements regarding the safety of using polymers and their composites are related to the emergence of more effective, sustainable, and hazardous-limited fire retardants (FRs). Significant amounts of FRs are usually required to effectively affect a polymer's burning behavior, while the knowledge of their recycling potential is still insufficient. At the same time, concerns are related not only to the reduced effectiveness of flame retardancy but also, above all, to the potential deterioration of mechanical properties caused by the degradation of temperature-affected additives under processing conditions. This study describes the impact of the four-time reprocessing of bio-based polyamide 11 (PA11) modified with an intumescent flame-retardant (IFR) system composed of ammonium polyphosphate (APP), melamine cyanurate (MC), and pentaerythritol (PER) and its composites containing additional short basalt fibers (BFs). Composites manufactured via twin-screw extrusion were subjected to four reprocessing cycles using injection molding. A comprehensive analysis of their structural, mechanical, and fire behavior changes in each cycle was conducted. The obtained results confirmed the safety of using the proposed fire-retarded polyamide and its composites while reprocessing under the recommended process parameters without the risk of significant changes in the structure. The partial increase in flammability of reprocessed PA-based materials caused mainly by polymer degradation has been described.

Research on preparation and performance tests of the fire retardant coatings for special functionalized wires and cables

This study aimed to produce a new potential intumescent flame retardant system through the addition of titanium dioxide and alumina-silica fiber based on optimizing the traditional ammonium polyphosphate (APP) / melamine (MEL) / pentaerythritol (PER) intumescent flame retardant formula. The flame retardant capacity and the physical properties were fully analyzed and discussed. The produced flame retardant coating could resist the rapid rise in 1100 of high flame temperature, whereas 40 exceeded the national standards. Thus, the produced flame retardant coating in this study could be potentially further applied to the cables and wires that are frequently needed in petroleum, telecommunication, military, tunnel, and electric uses.

P/N synergistic integrated flame retardants with instant cross-linking at high-temperature for flame retardancy and impact resistance of epoxy resins

With the development of flame retardant technology, intumescent flame retardant (IFR) systems, and instant cross-linking in case of fire have become important directions for epoxy resin (EP) flame retardancy. A carbonized matrix containing a benzoxazine structure was constructed with the triazine structure, and the integrated flame retardant (TRBPO) was constructed by introducing the phosphorus source through a partial ring-opening reaction. It can maintain its structural characteristics during the curing process of EP. When EP materials are exposed to fire, TRBPO will cross-link in the EP matrix and work as the P/N synergistic IFR system to achieve excellent flame retardancy. The results showed that 5 wt% of TRBPO could make EP composites reach UL-94 rating of V-0 with a PHRR of 303.7 kW/m2, and the TSP and TSR were reduced by 48.5 % and 48.9 %, respectively, compared with pure EP. The introduction of TRBPO has a impact resistance effect on EP, and its excellent stress dispersion effect made the impact strength of 5-TRBPO/EP reached 36.49 KJ/m2. The analysis of the flame retardant mechanism proved that the rapid carbon formation function of IFR and the self-crosslinking flame retardancy of TRBPO in the fire are the main reasons for flame retardancy. In addition, the capture of flammable groups in the gas phase is an important source of flame retardant effect.

Interface construction of phosphorus-based hybrid with micro/nano hierarchical structure toward intumescent flame-retardant epoxy resins with robust mechanical properties

The facile strategy for constructing phosphorus-based hybrid (APP@Zn-PT) is proposed to the simultaneous optimization of flame-retardant properties and mechanical properties of epoxy resins (EP), which is a long-term concern for the intumescent flame-retardant systems. Herein, APP@Zn-PT was fabricated via the assembly of nano-sheet phosphorus-containing triazole-zinc complex (Zn-PT) on the surface of ammonium polyphosphate micro-particles (APP). Notably, EP modified with APP@Zn-PT synchronously displayed highly fire-safe performance and excellent mechanical properties, which is seldom found in the traditionally intumescent flame-retardant EP systems. In the presence of 7 wt% APP@Zn-PT, EP acquired a high limiting oxygen index (LOI) of 31.1 %, and succeeded to meet the requirement for a UL-94 V-0 rating. Meanwhile, the results of cone calorimeter test (CCT) showed that the crucial parameters involving smoke production and heat release of EP/APP@Zn-PT presented significant decrease, that total smoke production (TSP) was dropped from 55.7 m2 of EP to 36.2 m2, and the peak of heat release rate (PHRR) was decreased from 1156 to 384 kW/m2. In addition, the interfacial interaction of APP@Zn-PT in epoxy matrix was improved as compared to APP due to the embedment of nano-sheet Zn-PT, which possessed reinforcing effect as well, and thereby the mechanical performances of EP/APP@Zn-PT were superior to neat EP and EP/APP. Generally, this work lays a foundation for the construction of phosphorus-based micro-nano hybrids, showing a great potential in high-performance polymers for practical application.

Fully bio-based intumescent flame retardant hybrid: A green strategy towards reducing fire hazard and improving degradation of polylactic acid

Polylactic acid (PLA) is a promising renewable polymer material with excellent biodegradability and good mechanical properties. However, the easy flammability and slow natural degradation limited its further applications, especially in high-security fields. In this work, a fully bio-based intumescent flame-retardant system was designed to reduce the fire hazard of PLA. Firstly, arginine (Arg) and phytic acid (PA) were combined through electrostatic ionic interaction, followed by the introduction of starch as a carbon source, namely APS. The UL-94 grade of PLA/APS composites reached V-0 grade by adding 3 wt% of APS and exhibited excellent anti-dripping performance. With APS addition increasing to 7 wt%, LOI value increased to 26 % and total heat release decreased from 58.4 (neat PLA) to 51.1 MJ/m2. Moreover, the addition of APS increased its crystallinity up to 83.5 % and maintained the mechanical strength of pristine PLA. Noteworthy, APS accelerated the degradation rate of PLA under submerged conditions. Compared with pristine PLA, PLA/APS showed more apparent destructive network morphology and higher mass and Mn loss, suggesting effective degradation promotion. This work provides a full biomass modification strategy to construct renewable plastic with both good flame retardancy and high degradation efficiency.

Enhance the fire safety of epoxy resin using ammonium polyphosphate flame retardant with the sandwich structure containing catalytic carbon formation function

AbstractAmmonium polyphosphate (APP) is often used to construct intumescent flame retardant systems together, but it is faced with the problem of adding too much flame retardant. This paper envisions the construction of a modified APP flame retardant (TR@ZIFAPP) with a sandwich structure by the method of covering, which, in order to endow APP flame retardant with better flame retardant effect. By constructing a metal catalytic layer and a triazine carbon formation layer, the modified APP flame retardant has both catalytic carbon formation and phosphorus–nitrogen synergistic flame retardant functions. TR@ZIFAPP is expected to be used in flame‐retardant polymer composites with low addition requirements, adding it to epoxy resin (EP) reveals that the TR@ZIFAPP flame retardant could achieve the optimal flame retardant effect when the addition amount was only 3 wt%. The UL‐94 rating reached V‐0 grade, and the two off‐fire auto‐ignition time levels were only 0.7 s. The analysis of its flame retardant mechanism showed that the flame retardant in EP was mainly through the rapid formation of carbon to isolate oxygen and dilute the flammable gas to reach a strong flame retardant effect.

Improved flame resistance and thermal insulation properties of steel fireproof coatings based on polyvinyl alcohol @ expandable graphite

Intumescent fireproof coating (IFC) can effectively slow down the temperature rise of base materials by constructing intumescent heat isolation chars. Expandable graphite (EG), combined with a typical intumescent flame-retardant system, shows an excellent expansion effect. However, it is difficult to be evenly dispersed in the coating system due to its low surface energy, thus limiting its application in IFC. In this research, EG encapsulated by polyvinyl alcohol (PVA) film was used in combination with conventional intumescent flame retardants to prepare a fireproof coating. Due to the increased hydrophilicity caused by the hydroxy groups of the PVA, both the dispersion and adhesion of EG can be greatly improved in the coating. Additionally, PVA also plays the role of a charring agent to further upgrade the quality of the produced carbon layer. The prepared IFC displays a satisfying synergistic effect. The experimental results showed that the back-surface temperature of the steel plate coated by PVA@EG was reduced to 232 °C after 20 min, far lower than the 250 °C of the unmodified EG system, and the thermal insulation performance was enhanced significantly. Compared with the untreated EG coating, the HRR, THR, and TSR decreased by 79.5 %, 86.0 % and 24.8 %, respectively, and combustion and smoke suppression performance were improved greatly. All in all, PVA@EG endows the coating with superior flame-retardant and thermal insulation performance and greatly improves the safety of steel structures in buildings.

A zinc-embedded multicomponent copolymer customized for polypropylene and its synergistic flame-retardant effect and outstanding mechanical properties

The poor compatibility between the common polar intumescent flame-retardant system (IFR) and the nonpolar polypropylene (PP), as well as the high additive amount, seriously impacts the mechanical properties of the composites. This study introduced collaborative flame-retardant technology to construct block copolymer flame retardants and prepared a zinc-embedded multicomponent copolymer (PM-Zn2+) customized for PP composites. In the PM-Zn2+ system, zinc oxide was embedded into the copolymer composed of piperazine phosphate oligomer and melamine phosphate. PM-Zn2+ exhibited an amorphous structure with extremely low crystallinity and demonstrated specific morphological adaptability. The PM-Zn2+ were well dispersed in the PP matrix and changed their morphology during processing. When applied to PP, excellent flame retardancy and mechanical properties were obtained by using a minimal amount of flame retardants (20 %). PM-2 %Zn2+ gave PP an LOI value of 31.5 %, and achieved a UL94 V-0 rating (1.6 mm thick), exhibiting a lower heat release rate and smoke release. The flame-retardant mechanisms of PM-Zn2+ mainly involved the synergistic and aggregative effects. Transition metal zinc synergistically interacted with polyphosphate groups to create a charring barrier effect and enhance synergistic smoke suppression, leading to a significant reduction in combustion intensity. In comparison to the Mix-Zn/PP composites, the mechanical properties of PM-Zn2+/PP were significantly enhanced due to the specific morphological adaptability and improved compatibility. The elongation at break increased significantly from 15.6 % to 627.9 %, marking a remarkable improvement of 40-fold improvement, while the impact strength rose from 23.7 kJ/m2 to 54.3 kJ/m2, representing a 129 % enhancement. Finally, the zinc-embedded multicomponent block copolymer offers a promising approach to developing high-performance flame-retardant polypropylene materials.

Preparation and Characterization of Microencapsulated Ammonium Polyphosphate with Polyurethane Shell and Its Flame Retardance in Polypropylene

Polypropylene (PP) shows no charring ability in burning due to the lack of hydroxyl functional groups; thus, the flame retardant system needs an additional amount of carbonizing agent. An ammonium polyphosphate (APP)-based all-in-one intumescent flame-retardant system was prepared by the in situ polymerization of polymeric methylene diphenyl diisocyanate (pMDI) with a glycerol-based and a glycerol–sorbitol-based polyol of high OH value. The microencapsulated APP with a polyurethane shell (MCAPP) of different polyols was characterized. The MCAPP with speculated improved flame retardant performance was selected for further evaluation in the PP matrix at different loadings by means of standard flammability tests.

A honeycomb-inspired carboxymethyl chitosan-covalently link NH2-black phosphorene biobased cellulose green nanocomposites with tremendously enhancement fire safety and thermal conductivity

Biobased carboxymethyl chitosan-modified black phosphorene (BP-CMC) was prepared through an amidation reaction between amino group functionalized black phosphorene (NH2-BP) and CMC. Density functional theory (DTF) express that the adsorption energy between urea and phosphene is −6.28 eV, indicating a strong interaction. The resulting BP-CMC was further applied to reinforce the mechanical, flame-retardant and thermal conductivity performance of honeycomb cellulose nanofiber (CNF) film via vacuum filtration. Cone calorimetry test (CCT) result exhibits that the introduction of 30 wt% BP-CMC significantly promoted the fire safety of CNF. For instance, a 98.41% reduction in smoke production rate (SPR), 92.00 % decline in CO release and a 61.31% decrease in heat release rate (HRR) were observed compared to neat CNF. Furthermore, Thermogravimetric infrared (TG-IR) indicates a significant decrease in the release of flammable gases. Raman spectra verify that the incorporation of 30 wt% BP-CMC improves the graphitization degree of residual chars, thus limiting the transfer of heat and oxygen. The improvement in fire safety is attributed to the formation of an intumescent flame-retardant system, which is rich in carbon source (CMC), acid source (BP) and gas source (amino). Simultaneously, the introduction of 30 wt% BP-CMC into CNF leads to considerable enhancement in thermal conductivity (up to 17.49 %), thermal diffusion (utmost to 43.45 %) and heat capacity (increased by 19.23 %). Moreover, the 30 wt % addition of BP-CMC into CNF possesses excellent mechanical properties with the improvement of toughness (increased by 143.50 %) and tensile strength (increased by 140.90 %). This strategy not only provides a new strategy for functionalizing BP but also upgrades the application potential of BP nanosheets in the fire safety of polymer composite films.

Synergistic Modification of Polyformaldehyde by Biobased Calcium Magnesium Bi-Ionic Melamine Phytate with Intumescent Flame Retardant.

Intumescent flame retardants (IFRs) are mainly composed of ammonium polyphosphate (APP), melamine (ME), and some macromolecular char-forming agents. The traditional IFR still has some defects in practical application, such as poor compatibility with the matrix and low flame-retardant efficiency. In order to explore the best balance between flame retardancy and mechanical properties of flame-retardant polyformaldehyde (POM) composite, a biobased calcium magnesium bi-ionic melamine phytate (DPM) synergist was prepared based on renewable biomass polyphosphate phytic acid (PA), and its synergistic system with IFRs was applied to an intumescent flame-retardant POM system. POM/IFR systems can only pass the V-1 grade of the vertical combustion test (UL-94) if they have a limited oxygen index (LOI) of only 48.5%. When part of an IFR was replaced by DPM, the flame retardancy of the composite was significantly improved, and the POM/IFR/4 wt%DPM system reached the V-0 grade of UL-94, and the LOI reached 59.1%. Compared with pure POM, the PkHRR and THR of the POM/IFR/4 wt%DPM system decreased by 61.5% and 51.2%, respectively. Compared with the POM/IFR system, the PkHRR and THR of the POM/IFR/4 wt%DPM system were decreased by 20.8% and 27.5%, respectively, and carbon residue was increased by 37.2%. The mechanical properties of the composite also showed a continuous upward trend with the increase in DPM introduction. It is shown that the introduction of DPM not only greatly reduces the heat release rate and heat release amount of the intumescent flame-retardant POM system, reducing the fire hazard, but it also effectively improves the compatibility between the filler and the matrix and improves the mechanical properties of the composite. It provides a new approach for developing a new single-component multifunctional flame retardant or synergist for intumescent flame-retardant POM systems.

Optimization of intumescent flame retardant system based on ammonium polyphosphate, double pentaerythritol, and zinc borate for thermoplastic polyurethane composite

AbstractThe widespread industrial applications of thermoplastic polyurethane (TPU) are partially limited by its flammability. The design of high‐performance intumescent flame retardants (IFR) is of great significance for enhancing flame retardant (FR) performance of TPU. In this work, an IFR system consisting of ammonium polyphosphate (APP), double pentaerythritol (DPER), and zinc borate (ZB) is proposed. The optimized experimental parameters with 15 wt.% additive amount of FR, APP‐DPER weight ratio of 2.28:1 and 15.56 wt.% ZB content are regulated based on Box–Behnken design‐response surface methodology (BBD‐RSM) to obtain TPU/FR composite with superior limiting oxygen index value of 30.2%. Noticeably, the design efficiency of TPU/FR composite is significantly improved by utilizing BBD‐RSM. Results of vertical burning test show that the optimized TPU/FR composite passes UL 94 V‐0 rating and peak heat release rate is dramatically reduced from 1355.88 (neat TPU) to 201.01 KW/m2 through cone calorimeter test. In addition, scanning electron microscopy accompanied with Raman spectroscopy are conducted to characterize the morphology and composition of residual char for further exploring the FR mechanism of IFR system in TPU. The as‐prepared TPU/FR composite has provided new potential application in engineering fields.

Use of intumescent flame-retardant systems in epoxy adhesives for debonding purpose

This work investigates the use of intumescent flame-retardant additives as a new debonding solution to disassemble bonded aluminum substrates. Melamine polyphosphate (MPP) or ammonium polyphosphate (APP) was incorporated into an epoxy adhesive joint as both an acid source and a swelling agent with this stimulus responsive behavior being triggered by heating. The ability of the system containing intumescent additives to swell and foam under heat radiation was efficiently exploited to provide enough local pressure to induce porosities and cracks at the interface, facilitating the disassembling of bonded aluminum substrates. Several aluminum/intumescent-epoxy/aluminum laminates were assembled and tested to assess the influence of the MPP and APP content on the mechanical strength of the joints. The structural, morphological, mechanical, and thermal properties of these modified epoxy resins and assemblies with aluminum substrates were studied using Scanning Electron Microscopy (SEM), a pull-off test, Differential Scanning Calorimetry (DSC), and Thermogravimetric Analysis (TGA). The ability of the intumescent-modified joints to support temperature-controlled debonding was evaluated using an oven. The lower debonding temperatures found were comparable to laminates with unmodified epoxy joint systems. Our patented debonding on-demand technology, based on an intumescent flame-retardant system, represents a promising treatment for multi-material structures and will enable products to be recycled at the end of their service life.

Grafting modification bamboo kraft lignin and its performance in rigid polyurethane foams

AbstractIn order to improve the efficiency of intumescent flame retardant (IFR), bamboo kraft lignin (BKL) was chemically functionalized by grafting melamine (MEL) and diethyl phosphite (DEP) and used for rigid polyurethane (RPU) foam. The BKL, MEL, and DEP in IFR system were used as char forming agent, gas, and acid source, respectively. The FTIR and XPS results indicated that the nitrogen (N) and phosphorus (P) containing BKL was successfully synthesized. The limiting oxygen index (LOI) value of N‐BKL and N/P‐BKL RPU foams were higher than BKL RPU foam, suggesting that N‐BKL and N/P‐BKL improved flame retardancy of the foams. The total heat release (THR), heat release rate (HRR), effective heat of combustion (EHC), and fire growth rate (FIGRA) values of N‐BKL and N/P‐BKL RPU foams were much lower than that of BKL RPU foam. The flame retardancy index value of N/P‐BKL RPU foams was higher comparing to N‐BKL RPU foam. These results indicated that the synergistic interaction between N containing compound of MEL and P containing compound of DEP led to the improvement flame retardant properties. Comparing to BKL RPU foam, the N/P‐BKL RPU foam increased 74°C of maximum weight loss temperature and decreased 18.1 wt% of mass loss, indicating enhanced thermal stability. The morphology of char after cone calorimeter testing showed the N/P‐BKL RPU foam presented more continuous and compact char residues, which could reduce heat and mass transfer, protecting underlying materials from further combustion in a fire, thus resulting in good flame retardancy and thermal stability properties. This work suggests a promising route to enhancing the flame‐retardant performance of RPU foam using nontoxic and more environmentally friendly grafted bamboo lignin.

Application of Polyethylene Glycol-Based Flame-Retardant Phase Change Materials in the Thermal Management of Lithium-Ion Batteries.

Composite phase change materials commonly exhibit drawbacks, such as low thermal conductivity, flammability, and potential leakage. This study focuses on the development of a novel flame-retardant phase change material (RPCM). The material's characteristics and its application in the thermal management of lithium-ion batteries are investigated. Polyethylene glycol (PEG) serves as the medium for phase change; expanded graphite (EG) and multi-walled carbon nanotubes (MWCNT) are incorporated. Moreover, an intumescent flame retardant (IFR) system based on ammonium polyphosphate (APP) is constructed, aided by the inclusion of bio-based flame-retardant chitosan (CS) and barium phytate (PA-Ba), which can improve the flame retardancy of the material. Experimental results demonstrate that the RPCM, containing 15% IFR content, exhibits outstanding flame retardancy, achieving a V-0 flame retardant rating in vertical combustion tests. Moreover, the material exhibits excellent thermomechanical properties and thermal stability. Notably, the material's thermal conductivity is 558% higher than that of pure PEG. After 2C and 3C high-rate discharge cycles, the highest temperature reached by the battery module cooled with RPCM is 18.71 °C lower than that of natural air-cooling; the material significantly reduces the temperature difference within the module by 62.7%, which achieves efficient and safe thermal management.

Synergistic flame retardancy of 4A-zeolite/MF-THEIC/ammonium polyphosphate in PP

In this paper, a melamine formaldehyde resin modified with tris(2-hydroxyethyl) isocyanurate (THEIC), named MF-THEIC, was synthesized via a solid-phase reaction between hexahydroxymethyl melamine (HMM) and THEIC. MF-THEIC was firstly used as a charring agent in an intumescent flame-retardant system together with APP as well as 4A-zeolite in flame-retarding PP. APP/MF-THEIC (3/1) can effectively reinforce the flame retardancy of PP at a total 24.0 % additive amount, moreover, 1.5 % 4A-zeolite is sufficient to achieve an optimum synergistic effect. The corresponding composites (Sample-17) had passed UL-94 V-0 classification well. The synergistic flame-retarding mechanism was systematically investigated by SEM, 31P NMR, TGA, FTIR spectra, and TG-MS. 4A-zeolite can react with APP to generate highly-active phosphates with good catalytic efficacy on polyphosphate esterification, and then to promote the formation of the char layer, simultaneously, 4A-zeolite is helpful to enhance the char graphitization degree and the strength of the intumescing char layer, thereby reinforcing its flame retardancy via a synergistic effect.

Preparation of a novel Fe‐MOF as the flame retardant synergist and its application in polystyrene

AbstractIn this work, a metal organic framework (Fe‐MOF) with the effect of absorbing toxic gases and good compatibility was synthesized by chelating a novel organic ligand contained carbonization groups (reacted by tris(hydroxymethyl) aminomethane and 1,4‐piperazine dialdehyde) with iron salt. Then, it was used as the synergist to improve the efficiency of intumescent flame retardant (IFR) within polystyrene (PS) substrate. With the addition of 20% IFR and 2% Fe‐MOF, the obtained PS composites exhibited a limiting oxygen index (LOI) value of 28.3% and a UL rating of V‐0. Moreover, the peak heat release rate (pHRR), total heat release (THR), and total smoke production (TSP) of PS composites were decreased by 77.6%, 35.2%, and 33.7%, respectively. According to the mechanism analysis, it was found that Fe‐MOF mainly acted in the condensed phase, contributing to the existence of dense char residues with the presence of IFR system. In addition, the good compatibility of organic ligand in Fe‐MOF with PS substrate could partially alleviate the deterioration of mechanical properties due to the addition of IFR. For PS‐20%IFR/2%Fe‐MOF, the impact strength was improved from 1.7 kJ/m2 (PS‐22%IFR) to 2.2 kJ/m2, the tensile strength was also increased from 21.3 MPa (PS‐22%IFR) to 22.4 MPa.