Research progress of flame retardant modified polycarbonate/acrylonitrile butadiene styrene alloys: a review
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- Accepted
- Received
- Academic Editor
- Junkuo Gao
- Subject Areas
- Composites, Polymers
- Keywords
- Polycarbonate/Acrylonitrile Butadiene Styrene alloys, Flame retardant, Phosphorus-based flame retardant, Co-effect flame Retardant, Literature review
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- © 2025 Zhang et al.
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- This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits using, remixing, and building upon the work non-commercially, as long as it is properly attributed. For attribution, the original author(s), title, publication source (PeerJ Materials Science) and either DOI or URL of the article must be cited.
- Cite this article
- 2025. Research progress of flame retardant modified polycarbonate/acrylonitrile butadiene styrene alloys: a review. PeerJ Materials Science 7:e39 https://doi.org/10.7717/peerj-matsci.39
Abstract
This paper focuses on the current status and significance of research on flame-retardant modified polycarbonate/acrylonitrile butadiene styrene alloys (PC/ABS). PC/ABS alloys, as a kind of widely used modified engineering plastics, have many advantages, but their poor flame-retardant properties limit the applications. Flame retardants can give flammable polymers flame retardant properties and reduce the risk of fire, thereby mitigating potential environmental damage from uncontrolled burning and toxic fume release. This review focuses on the current research status of additive flame retardants, which are the most widely used in the current market, mainly including phosphorus-based, silicone-based and synergistic flame retardants. This review finds that in the future, flame retardant PC/ABS will develop in the direction of increasing market demand, improving environmental protection requirements (e.g., seeking halogen-free alternatives and enhancing material recyclability), and relying on technological innovations such as nanomaterials and renewable additives to optimize flame retardancy and overall performance. These advancements contribute significantly to developing safer and more environmentally sustainable materials.
Introduction
Rationale, scope, and target audience
Polycarbonate/acrylonitrile butadiene styrene alloys (PC/ABS alloys), as a class of widely utilized modified engineering plastics, combine the advantageous properties of polycarbonate (PC)—such as high impact strength, transparency, and heat resistance—with the excellent processability, cost-effectiveness, and toughness of acrylonitrile-butadiene-styrene (ABS) (Fig. 1). This synergy makes them indispensable in demanding applications across electronics (e.g., laptop housings, mobile phone components), automotive interiors (e.g., dashboards, trim pieces), and electrical enclosures. However, a critical limitation hindering their broader application, particularly in sectors with stringent fire safety regulations (e.g., IEC 60332-1 for wires/cables, FMVSS 302 for automotive interiors, UL standards for consumer electronics), is their inherent flammability. Unmodified PC/ABS exhibits a low limiting oxygen index (LOI), achieves only an HB rating in the Underwriters Laboratories 94 Vertical Burning Test (UL-94 vertical burning test), produces significant heat release, Peak Heat Release Rate (PHRR) is approximately 800–1,000 kW/m2, and generates toxic gases (HCN, CO) and flaming droplets upon ignition, posing substantial fire hazards.
Figure 1: Schematic diagram of the microstructure of PC/ABS alloy (Sea-Island phase structure).
This schematic illustrates the phase morphology of a PC/ABS blend, where PC forms the continuous phase and ABS (containing rubber toughening particles) constitutes the dispersed phase.Consequently, enhancing the flame retardancy (FR) of PC/ABS alloys is not merely an academic pursuit but a critical industrial necessity driven by safety regulations, environmental concerns (phasing out halogenated FRs), and market demand for safer, high-performance materials. Research into flame-retardant modified PC/ABS has surged, exploring diverse FR systems from traditional halogens to advanced phosphorus, silicon, and synergistic combinations. This review aims to synthesize the current state of knowledge in this rapidly evolving field.
Literature search methodology
To ensure a comprehensive, unbiased, and up-to-date coverage of the literature on flame-retardant modified PC/ABS alloys, a systematic search strategy was employed. This systematic approach aimed to gather a representative body of high-quality literature, enabling a critical synthesis of the current research status, key findings, challenges, and future directions in flame-retardant modification of PC/ABS alloys. Through the comprehensive search strategy described above, a total of 120 relevant records were initially identified. The flow diagram of the literature screening and selection process is presented in Fig. S1 (PRISMA flow diagram).
Background on PC/ABS and flame retardancy need
In modern production and life, polymer materials covering plastics, rubber, fibers and other categories could be found everywhere in industry, agriculture and daily life, and they had become an indispensable part of daily life, from cutting-edge technology in national defense to key industries such as electricity, construction and transportation (Tang et al., 2017; Tang et al., 2013). Flame retardants, as a functional modification additive, were widely used in natural or synthetic polymer materials, and their use was second only to plasticizers (Wang, Yang & Guo, 2023). It had the ability to transform flammable polymers into a flame-retardant or even non-flammable state, thus effectively reducing the huge loss of life and property caused by fire (Sadeghzadeh et al., 2024; Zylstra et al., 2023; Liang, Neisius & Gaan, 2013; Realinho et al., 2014).
PC excelled in the field of material science by virtue of its excellent mechanical properties such as high toughness and high strength (Song et al., 2022), good electrical insulation and relatively high glass transition temperature (Moslan et al., 2021). ABS had good impact resistance, toughness and processability (Li et al., 2020). However, its weathering and flame-retardant properties were not as good as they should be (Huang et al., 2018). Therefore, the alloy obtained by blending PC and ABS resin combined the advantages of PC and ABS resin (Reby Roy et al., 2022). The resulting PC/ABS alloy had an improved melt flow rate and better processability than PC (Zuo et al., 2025). Due to the presence of the ABS component, the flame retardant performance of PC/ABS alloys is significantly inferior to that of pure PC (Huang et al., 2018; Realinho et al., 2018; Rahbari et al., 2018). This has made improving their flame resistance through modification a valuable and widely researched topic, attracting significant attention from both industry and academia. Cone calorimetry tests confirm that its peak heat release rate (PHRR) reaches 800–1000 kW/m2, and the fire hazard is 2–3 times that of the flame-retardant modified system. These characteristics make it difficult to meet the mandatory flame retardant standards in the fields of electronic appliances (such as IEC 60332-1) and automobiles (FMVSS 302), and urgently requires flame retardant modification to enhance safety (Table S1).
Studies on the mechanisms of flame-retardant modified PC/ABS alloys
In order to better grasp the information related to flame-retardant modification, firstly, it is essential to comprehensively grasp the combustion process of polymeric substances as well as the flame-retardant mechanisms of PC/ABS. The combustion of polymer materials usually produced highly reactive hydrogen radicals and hydroxyl radicals, and some flame retardants inhibited combustion by removing the above radicals (Zukowski & Berkowicz, 2019). The material itself released substantial heat during combustion (Fig. S2), creating a self-sustaining feedback loop. Once the heat release rate was sufficient to maintain polymer decomposition, combustion could continue without an external heat source until the material was consumed (He et al., 2020).
The flame retardancy of PC/ABS alloys operates through both gas-phase and condensed-phase mechanisms. In the condensed phase, retardants promote PC carbonization and Fries rearrangement, leading to cross-linking (Liu et al., 2020). In the gas phase, they act by releasing inert gases to dilute oxygen and dissipate heat, and by producing radicals (e.g., PO⋅, HX) that scavenge highly reactive H⋅ and OH⋅ radicals to quench the combustion chain reaction (Parkinson, 2016). Furthermore, the material’s own combustion heat provides feedback for sustained burning (Table S2). Critically, the thermal decomposition of PC/ABS exhibits a significant synergistic effect between its components (Fig. S3), enhancing its overall flame retardancy.
Recent advances in flame-retardant modifications of PC/ABS alloys
Overview of flame-retardant modification for PC/ABS
Flame retardants are substances that impart flame retardancy to flammable polymers and reduce the risk of fire. It is found that there are two main types of flame-retardant modification of PC/ABS alloys: intrinsic flame-retardant modification method and additive modification method (Liu et al., 2021).
The additive modification method, which involves directly blending flame retardants with the substrate, is widely adopted due to its operational simplicity, cost-effectiveness, and suitability for large-scale industrialization. Consequently, extensive research has been conducted on various flame retardants, each with its own distinct advantages and limitations, as none are without drawbacks.
Halogenated flame retardants
Halogenated flame retardants were once extensively applied because of their remarkable flame-retardant efficiency, excellent thermal stability, abundant raw materials, and affordable prices (Liu et al., 2019; Abd El-Wahab, 2015; Badea et al., 2016). Halogenated flame retardants released a refractory gas, H-X, during combustion, and it was more dense (Hu et al., 2011; Liu et al., 2024). It was able to coat the surface of the material, thereby serving as a barrier against heat and oxygen. Moreover, only a small quantity of halogenated flame retardant needed to be added to endow the material with excellent flame-retardant properties.
Seddon & Harper (2001) conducted a study examining how Tetrabromobisphenol A (TBBPA) and Sb2O3 affected the properties of ABS. The study showed that the notched impact strength of ABS increased when the Sb2O3 particle size approached 0.1 µm. Petsom and other scholars (Petsom et al., 2003) chose 1,2-bis(2,4,6-tribromophenyl) ethane for the flame-retardant treatment of ABS. The results indicated that the flame retardant exerted a substantial influence on the notched impact strength and heat deflection temperature of ABS. However, it had a negligible impact on the tensile and flexural strengths (Wang et al., 2025). While applying halogenated flame retardants to PC/ABS alloys could yield relatively good flame-retardant outcomes (Wang et al., 2015), these flame retardants produced toxic gases during combustion. Such gases posed risks to both the environment and human health (Ullrich et al., 2022). Previously, the use of halogenated flame retardants was being phased out (Table S3) (Lee et al., 2022; Aznar-Alemany et al., 2019).
Flame-retardant modification of PC/ABS using phosphorus-based flame retardants
Previously, among flame retardants, phosphorus-based flame retardants were the most widely used in the market besides halogenated ones (Badea et al., 2016). They were more environmentally friendly than their halogen-based counterparts, emitting less smoke and exhibiting lower toxicity (Aznar-Alemany et al., 2019; Han et al., 2023; Chen et al., 2022).
Inorganic phosphorus flame retardants
Inorganic phosphorus-based flame retardants included substances like red phosphorus, microencapsulated red phosphorus, and ammonium polyphosphate (APP) (Kim et al., 2025; Li et al., 2014), ihibited combustion by releasing phosphorus compounds. Although red phosphorus was highly efficient, it had poor compatibility with resins and was dark in color, which limited its use in light-colored products (Pawlowski & Schartel, 2007; Xu et al., 2021). Microencapsulated red phosphorus improved this problem, while APP was widely used in several industries due to its good thermal stability and light color characteristics. Shi et al. achieved flame retardancy in a 7:3 PC/ABS alloy using a blend of eight parts pentaerythritol (PER), magnesium hydroxide (Mg(OH)2), aluminum hydroxide (Al(OH)3), and 22 parts ammonium polyphosphate (APP). This formulation resulted in a high limiting oxygen index (LOI) of 33%, revealing a significant synergistic flame-retardant effect between PER and APP.
Organophosphorus flame retardants
Organic phosphorus flame retardants were also widely applied as phosphorus-based flame retardants in PC/ABS (Despinasse & Schartel, 2013). Commercially produced phosphate ester flame retardants included bisphenol A-bis(diphenyl phosphate) (BDP), triphenyl phosphate (TPP), and resorcinol bis (diphenyl phosphate) (RDP) (Despinasse & Schartel, 2013; Xie et al., 2017; Dueñas Mas, Ballesteros-Gómez & Rubio, 2020; Christia et al., 2018).
Wei et al. (2013) successfully prepared a new organic–inorganic hybrid mesoporous silica with 9,10-dihydro-9-oxa-10-phospha-phenanthrene-10-oxide (DOPO) (Fig. S4) terminal functionalization (denoted as DM) and compounded it with TPP for flame-retarding PC/ABS. The PC/ABS system containing 6 wt% TPP and 2 wt% DM exhibited notably enhanced flame retardancy, accompanied by the formation of a tightly compacted carbon layer. The DM/TPP synergy enhanced flame retardancy by altering the thermal degradation of PC/ABS, reducing heat release, and promoting a denser char layer. This establishes the hybrid mesoporous silica as an effective synergist that optimizes fire performance through this collaborative mechanism (Chen et al., 2024).
Silicon flame retardants
Silicone-based flame retardants have gained increasing attention due to their excellent flame retardancy, high mobility, good mechanical properties (notably excellent low-temperature impact strength), and advantages of low smoke and toxicity. They can be classified into organic and inorganic types. Although they excel in environmental protection, low toxicity, and low smoke emission, silicone-based flame retardants remain in the early R&D stage, with scarce market products that are costly (Camino, Lomakin & Lageard, 2002; Camino, Lomakin & Lazzari, 2001).
Inorganic silicon flame retardants
Inorganic silica flame retardants mainly contain montmorillonite, talc, silicon dioxide (SiO2) and silicates and other substances. Inorganic silica flame retardant is not effective when used alone, and should be used together with other flame retardants.
Zong et al. (2004) prepared organic montmorillonite (OMT) by the intercalation method, The results indicated that incorporating 5wt% OMT into the modified PC/ABS alloy improved its thermal stability and reduced flammability. This outcome was attributed to the nanodispersed silicate layers functioning as effective thermal insulators and mass transport barriers, which slowed the decomposition rate and elevated the decomposition temperature.
Organosilicon flame retardants
Organosilicon flame retardants generate SiO2 coverings during the combustion process, thus playing a dual role of thermal insulation and shielding. Silicone flame retardants mainly include polysiloxanes, silicone resins, silicone oils and silicone rubbers (Zong et al., 2005).
A study by Iji & Serizawa (2025) found that when 5% poly (methylphenylsiloxane) was added to PC and used in combination with PTFE, the LOI value increased progressively from 26% to 33% and further to 40%, demonstrating a significant enhancement in flame retardancy. and the vertical combustion class reached V0.
Synergistic flame retardants
While single-flame retardants often impair mechanical and processing properties at high loadings, combining different types can create a synergistic effect. This enhances efficiency, reduces required dosage, and ultimately improves both the cost-effectiveness and performance of the composite.
Synergistic flame retardancy of silicon-based and phosphorus-based flame retardants
Phosphorus-based flame retardants exhibit efficient flame-retardant effects on PC, while silicone-based flame retardants demonstrate notable flame-retardant efficacy in ABS (Zhong et al., 2007; Murashko et al., 1999; Mendis et al., 2016). Given this, the combination of phosphorus- and silicon-based flame retardants in PC/ABS materials represents a viable strategy (Wang et al., 2018; Vothi et al., 2025; Sun et al., 2023).
Feyz, Jahani & Esfandeh (2010) incorporated 2.0wt% nanoclay and 8.0wt% TPP into PC/ABS (65:35) to achieve a UL-94 V-0 flame retardant grade, attributed to the synergistic flame-retardant effect of the two components. The LOI was observed to increase with rising TPP content but decrease as nanoclay content increased (Lee et al., 2002). Another research team explored the blending of inorganic phosphorus-based and silicone-based flame retardants for flame-retardant PC/ABS. Mortelmans et al. (2022) added 0.7 wt% of red phosphorus as well as 9.0wt% of talc to a 7:3 mix of PC/ABS, and successfully achieved the UL-94 V-0 flame retardant rating for PC/ABS. This research outcome highlights the efficacy of blending inorganic phosphorus-based and silicone-based flame retardants for the flame-retardant modification of PC/ABS, successfully achieving the UL-94 V-0 rating. The findings offer a valuable reference for further development of high-efficiency flame-retardant PC/ABS materials, demonstrating the potential of synergistic flame-retardant systems in balancing fire safety and material performance.
Phosphorus-silicon-nitrogen synergistic flame retardant
Besides organophosphorus (Bee et al., 2025) compounds, nitrogen-containing and silicone-containing compounds are also classified as eco-friendly flame retardants due to their ability to generate fewer toxic and harmful byproducts. Recent studies have shown that the synergistic combination of these three flame-retardant elements (phosphorus, nitrogen, and silicon) in a flame-retardant system can endow the base material with superior flame-retardant properties (Gao et al., 2008).
Zhong et al. (2025) synthesized 9,10-propanoic acid (DPA) from DOPO and acrylic acid (AA). A novel flame retardant, DPA-SiN, was synthesized by introducing N-β-(aminoethyl)-γ-am-isopropylmethyldimethoxysilane/dimethylsiloxane copolymer (SiN). When added to PC/ABS alloys, the LOI increased from 21% to 27%, while both the heat release rate and total heat release were halved. Thermal decomposition formed a more stable char layer, which acted as a protective barrier to block heat and mass transfer during combustion. Ni et al. (2018) successfully synthesized a flame retardant (TPPSi) that combines both caged bicyclic phosphate groups and silicone structure, as well as the bulking agent polydimethylsiloxane-g-styrene-g-methyl methacrylate copolymer (PSM), when 8.0wt% of TPPSi was added to PC/ABS (9:1), the composite achieved a UL-94 V-0 flame retardancy rating.
Phosphorus-nitrogen flame retardant
In the field of PC/ABS flame retardant modification, phosphorus-nitrogen flame retardants are commonly used, which mainly include intumescent flame retardants and phosphonitrile flame retardants with alternating P-N main chains.
Chen, Wu & Qian (2020) developed a novel aniline-terminated phosphonitrile-triazine bis-alkyl flame retardant (A3). They proposed that A3 could facilitate the formation of a more complete and compact char layer during PC combustion, while releasing PO− radicals that exhibit flame-retardant activity in the gas phase. Feng, Qian & Lu (2021) successfully synthesized a new type of aromatic polyimide (API) carbonizing agent (shown in Fig. S5). This kind of carbonizing agent is mainly used to make up for the lack of toughness in the use of hexaphenoxycyclic triphosphonitrile (HPCTP) to enhance the flame retardant properties of PC, which is of great significance in the subsequent processing and industrial application of PC as a flame retardant synergist to improve the notched impact properties of PC.
Phosphorus-metal flame retardant
In addition to nitrogen, metallic elements can also be hybridized with phosphorus to provide a cohesive phase flame retardant system. Metal-based flame retardants can be broadly divided into inorganic metal hydroxide flame retardants and organo-metal flame retardants. At present, people are more interested in organic- metal flame retardants (such as metal-organic framework flame retardants, etc.). Under high temperature conditions, some specific metals or metal derivatives have the ability to catalyze carbon formation, and the main metal catalysts are: iron compounds, molybdenum compounds, zinc compounds, nickel compounds, and rare-earth compounds (Gao et al., 2025).
Sai et al. (2021) developed PC materials with excellent flame retardancy and high transparency. They successfully synthesized rod-shaped phosphorus-containing complexes (CeP) by a one-step solvothermal method. Adding 4wt% CeP to PC significantly reduced the peak heat release rate by 46%. The flame-retardant mechanism of CeP involves scavenging reactive radicals in the gas phase to suppress combustion and catalyzing char formation in the condensed phase to improve PC’s flame retardancy.
Phosphorus-sulfur flame retardant
Sulfur-containing compounds often have good fire-resistant properties (Ding & Hay, 1997), but few scholars have used them as independent PC/ABS flame retardants, and they are typically combined with phosphorus flame retardants to promote the decomposition of the latter during early pyrolysis.
Hou et al. (2021) partially replaced BDP with phosphonium sulfonate (PhS) in PC/ABS to mitigate the adverse effects of phosphorus flame retardants on the mechanical properties and pyrolysis resistance of PC/ABS. The results showed that PhS and BDP exhibited a synergistic flame-retardant effect, improving the quality of the char layer while maintaining the tensile properties, glass transition temperatures, and hydrolysis resistance of the composites without deterioration.
Carbon-metal flame retardant
Carbon-metal hybrid flame retardants are rarely reported in the flame retardancy of PC or ABS. When carbon-based flame retardants (e.g., graphene, carbon nanotubes, and carbon black) are applied to polymers, their main mode of action is the formation of a coke network structure, inhibiting heat and oxygen transfer to the matrix (Araby et al., 2021). Although carbon nanomaterials are promising both as stand-alone and synergistic additives, their relatively high cost has largely limited their popularization and application.
Layered double hydroxides (LDHs), also known as hydrotalc-like compounds, have the general formula [M2+1−xM3+x(OH)2]x+(An−x/n)⋅mH2O. Owing to their compositional flexibility, a diverse array of LDHs with distinct properties can be synthesized. In a study conducted by Hong et al. (2014), they successfully achieved the simultaneous enhancement of both mechanical and flame retardant properties in ABS by combining 2D graphene nanosheets (GNS) with 1D metal hydroxide nanorods (MHR).
Phosphorus-nitrogen-metal flame retardant
Phosphorus-nitrogen-metal flame retardants can exhibit multiple flame retardant mechanisms in both condensed and gas phases. Yuan et al. (2021) studied the synergistic effects of piperazine pyrophosphate (PAPP) and aluminum diethylphosphite (AlPi) on improving ABS flame retardancy and proposed a synergistic mechanism for the two agents.
Huang et al. (2021) tackled the common degradation of mechanical and thermal properties of ABS caused by conventional flame retardants and developed a graphene-based flame retardant (Mo5/PN-rGO) incorporating phosphorus, nitrogen, and molybdenum. Notably, incorporating just 1.0wt% of Mo5/PN-rGO into ABS composites led to a substantial 45% reduction in total smoke release, along with simultaneous enhancements in tensile strength, Young’s modulus, and initial decomposition temperature. The team also proposed a corresponding flame retardant mechanism, wherein the flame retardant exhibits a primary role in the condensed phase and a secondary role in the gas phase. Upon decomposition at 400 °C, Mo/PN-rGO liberates non-flammable NH3 and H2O vapor, which exert a dilution effect to suppress gas-phase combustion of ABS.
This section focuses on hetero-elemental flame-retardant systems containing phosphorus. Recent years have witnessed substantial progress in phosphorus-based flame retardants, yet multiple challenges persist.
Comprehensive performance comparison of flame-retardant systems
The minimum modification conditions and key performance metrics of flame-retardant systems to achieve UL94 V-0 rating are compared in Table S4. Organophosphorus flame retardants (e.g., BDP) achieve the target UL94 V-0 rating at the lowest loading of 10wt%, exhibiting 1.5 × higher efficiency than halogenated systems while maintaining 85% impact strength retention—significantly superior to phosphorus-nitrogen synergistic systems (55–65%) (Greco & Sorrentino, 1994). Silicone-based flame retardants, leveraging flexible Si-O-Si chain structures, minimize impact strength loss (>85% retention) at merely 8 wt% loading. However, their flame-retardant efficiency (LOI: 32–40%) is constrained by dispersion homogeneity (Iji & Serizawa, 2025; Wei et al., 2009). Phosphorus-silicon synergistic systems (e.g., RDP + 5% nano-SiO2) demonstrate optimal balance: at 14 wt% total loading, LOI reaches 29–32%, peak heat release rate (PHRR) decreases by 70% (vs. unmodified), and melt dripping is completely eliminated, establishing them as the preferred solution for electronic device housings (Qiao et al., 2019). Future efforts should focus on surface modification of nano-SiO2 or developing reactive phosphorus-silicon compounds to reduce additive costs and enhance process stability.
The incorporation of flame retardants substantially alters the mechanical properties of PC/ABS alloys (Table S5): Organophosphorus systems (e.g., BDP, 10 wt%) demonstrate optimal balance—85% impact strength retention (38.2 kJ/m2) with only 9.8% tensile strength loss (52.3 MPa), attributed to plasticizing effects mitigating matrix embrittlement (Pawlowski & Schartel, 2007). Silicone-based retardants (8 wt%) achieve the highest impact retention (>85%, 41.3 kJ/m2) via stress dissipation through flexible Si-O-Si chains, though tensile strength decreases by 4.1% due to interfacial weakening (Wei et al., 2009). High-loading systems cause severe degradation: Phosphorus-silicon compounds (DPA-SiN, 30 wt%) reduce impact strength by 50% (22.5 kJ/m2) via phase separation, while phosphorus-nitrogen systems (APP/PER, 30 wt%) incur 36.4% tensile strength loss (36.9 MPa) (Zhong et al., 2025). Industrial selection guidelines are: organophosphorus for electronics housings (balanced performance), silicone for automotive interiors (high toughness), and avoidance of P-N/P-Si compounds in structural parts (>30% strength reduction).
Conclusion
PC/ABS alloy, as an important engineering plastic, its flame retardant modification research plays a significant role in enhancing material safety and expanding application fields. This paper systematically reviews the application status and mechanisms of phosphorus-based, silicon-based, halogen-based, and various synergistic flame retardant systems in PC/ABS. The research indicates that halogen-free flame retardant systems (such as phosphorus–silicon synergy, phosphorus–nitrogen synergy, etc.) exhibit remarkable advantages in terms of environmental friendliness, flame retardant efficiency, and the balance of comprehensive performance, and have become the focus of current research. In the future, the development of flame-retardant PC/ABS will place greater emphasis on the integration of environmental friendliness, high efficiency, and multifunctionality. Through the design of new materials and optimization of processes, it will promote their wider application in high-end fields such as electronics, automotive, and construction.
Significance of the study and future prospects
Significance of the study
The study of flame retardant-modified PC/ABS composites is of great significance, both academically and for promoting materials science and engineering (Table 1).
| Type of flame retardant | Typical representative | Flame retardancy efficiency (loading for UL94 V-0) | Impact on mechanical properties (impact strength retention) | Environmental impact (toxicity/sustainability) | Cost (material/ processing) |
|---|---|---|---|---|---|
| Halogenated flame retardants | TBBPA + Sb2O3 | 10–15 wt% | Significant reduction (<60%) | High toxicity, releases dioxins, HBr | Low material cost, high environmental treatment cost |
| Organophosphorus flame retardants | BDP, RDP, TPP | 10–12 wt% | Good (∼85%) | Low smoke, low toxicity, partially biodegradable | Moderate |
| Inorganic phosphorus flame retardants | Red phosphorus, APP | 14–21 wt% | Poor (prone to embrittlement) | Halogen-free, low toxicity, but red P poses dust explosion risk | Low |
| Silicone-based flame retardants | Polysiloxanes, MMT | 8–10 wt% | Excellent (>85%) | Low toxicity, low smoke, environmentally friendly | High (especially for organic silicones) |
| P-Si synergistic flame retardants | RDP + nano-SiO2 | 9 wt% RDP + 5% SiO2 | Good (>75%) | Low toxicity, low smoke | Moderate to high (nanomaterial cost) |
| P-N flame retardants | APP + Melamine | 20–30 wt% | Poor (<65%) | Halogen-free, but may release NH3 | Low to moderate |
| P-N-metal flame retardants | Mo5/PN-rGO | 1–2 wt% | Enhances mechanical properties | Low toxicity, high efficiency | High (complex synthesis of nanomaterials) |
| Carbon-metal flame retardants | GNS + Co(OH)2 | 1–3 wt% | Enhances mechanical properties | Low toxicity, sustainable | High (nanomaterial cost) |
| Bio-based flame retardants | Tannic Acid (TA) | 20–30 wt% | Under investigation | Fully bio-based, biodegradable | Low to moderate |
Safety is a prime concern. By applying suitable flame retardants, the fire-resistant properties of PC/ABS composites are enhanced. This reduces fire accidents, safeguards lives and property. The products can meet or exceed strict international standards like UL94 and IEC, ensuring market access. Their applications extend beyond consumer electronics to public transportation and medical equipment, sectors with strict safety regulations. Economically and socially, advances in flame retardant modification technology boost innovation and upgrading in the new materials industry while driving related industrial chains, generating employment and economic benefits, thus creating a positive feedback loop for society and the economy. A key focus of future research is the development of eco-friendly flame retardants. Though effective, traditional halogenated flame retardants pose environmental and health risks. So, there is a growing body of research on halogen-free alternatives like those based on silicon, nitrogen, and phosphorus, which are both efficient and eco - friendly.
In summary, developing and applying flame retardant-modified PC/ABS composites enhances safety, greener, and more efficient modern industrial system, promoting the coexistence of environmental protection and technology.
Future prospects
The future of flame retardant modified PC/ABS composites is highly promising. Research will focus on developing efficient, eco-friendly non-halogenated flame retardants such as phosphorus-based, nitrogen-based, silicone-based, and bio-based options from renewable resources. For instance, a recent study demonstrated that a novel DOPO-derived phosphaphenanthrene compound significantly enhanced flame retardancy in PC/ABS blends while maintaining mechanical performance. Combining various flame retardant types, like phosphorus-based and nitrogen-based ones, can achieve synergistic effects. A representative example is the use of ammonium polyphosphate (APP) with melamine cyanurate (MC), which has been shown to form an intumescent char layer that effectively inhibits heat and mass transfer during combustion. Nanomaterials like nanoclay and nanosilica can enhance both mechanical and flame retardant properties. Future flame retardants also need to have additional functions like antistatic, antibacterial, and weatherability to expand the application fields of PC/ABS composites (Watanabe et al., 2009), such as in battery shells of new energy vehicles, high-speed train interiors, and building cable sheathing. For example, a multifunctional composite integrating zinc oxide-based antibacterial agents and silicone-based flame retardants has been developed for use in high-touch public transport interiors.
With the growth of application areas, it’s crucial to establish unified international standards and test methods to regulate the market and ensure product quality and user safety. As countries tighten material flame retardant requirements, research must keep up with regulatory changes. Despite the high development costs of advanced flame retardants, process optimization and production scale-up can reduce costs and enhance competitiveness. Promoting the recycling of these composites is essential for resource recycling and environmental protection. Recent advances in chemical recycling techniques, such as aminolysis of PC/ABS blends, have shown promise in recovering high-purity monomers for reuse. From the perspective of Technology Readiness Level (TRL), various technologies for flame-retardant modification of PC/ABS are currently at different stages of development. Traditional halogen-based flame retardants, although technologically mature (TRL 9), are being phased out due to environmental concerns; organophosphorus flame retardants (e.g., BDP, RDP) have reached commercial application levels (TRL 8-9), while most silicon-based, phosphorus-silicon synergistic, and bio-based flame retardants are still in the laboratory research and pilot stages (TRL 3-6). In the future, efforts should focus on accelerating the industrialization process of high-TRL green flame retardant systems to promote the transition from laboratory innovation to large-scale application.
In the future, the development of flame retardant modified PC/ABS composites will focus on environmental friendliness, high performance, multifunctionality, and sustainability. This will contribute significantly to creating a safer, greener, and more efficient modern industrial system, providing better products and a better future for society.
Supplemental Information
Comparison of flame retardant mechanisms between PC and ABS
Data comparison between halogen-based and phosphorus-based flame retardants
Performance comparison of major flame-retardant systems for PC/ABS alloys (UL94 V-0 required)
Effects of representative flame retardants on mechanical properties of PC/ABS alloys
Outlines of the literature search and screening process
Outlines the literature search and screening process based on the PRISMA flow diagram, detailing the identification and inclusion of studies from Web of Science and CNKI for the quantitative synthesis.
Illustration of the combustion mechanism of a polymer
Illustrates the combustion mechanism of a polymer, detailing the key stages from thermal degradation in the condensed phase to flame reactions in the gaseous phase.
Details of the chemical mechanisms of gas formation during the thermal decomposition of PC and ABS
Details the chemical mechanisms of gas formation during the thermal decomposition of PC and ABS, illustrating how the resulting mixed flammable volatiles feed the combustion cycle.
Outline of the molecular modification process
Outlines the molecular modification process, depicting the conversion from the PPDC precursor to the PPSO structure in a TEA/THF solvent system.
