{"title":"Enhancing flame retardancy and mechanical performance of polycarbonate with cinnamate-containing liquid crystalline copolyester","authors":"Yao Yan, Zuanxin Yang, Songming Chen, Rong Yang","doi":"10.1016/j.polymdegradstab.2025.111675","DOIUrl":null,"url":null,"abstract":"<div><div>The flame-retardant modification of polymers, while preserving or enhancing their mechanical properties, is critical for engineering plastics. In this study, we develop flame-retardant polycarbonate (PC) composites with improved mechanical performance by incorporating cinnamate-containing liquid crystalline copolyester (CLCP). During the injection molding process, CLCP forms oriented microfibrils in situ, boosting the tensile strength of the composites by up to 66 %. The cinnamate groups in CLCP undergo radical-initiated thermal crosslinking, which increases melt viscosity, prevents dripping, and achieves a UL-94 V-0 rating. The primary flame retardancy mechanism occurs in the condensed phase: early decomposition of CLCP triggers thermal crosslinking, leading to the formation of a dense, graphitized char layer that reduces the peak heat release rate (PHRR) by 46.8 %, total smoke production by 17.9 %, and increases the limiting oxygen index (LOI) to 32.5 % (compared to 27.0 % for neat PC). This dual-functionality of CLCP addresses both the flammability and mechanical limitations of PC, making it a promising candidate for engineering applications requiring high-performance materials. This work introduces a novel molecular design strategy, integrating liquid crystallinity and cinnamate crosslinking, to enhance both flame resistance and mechanical properties in engineering plastics.</div></div>","PeriodicalId":406,"journal":{"name":"Polymer Degradation and Stability","volume":"242 ","pages":"Article 111675"},"PeriodicalIF":7.4000,"publicationDate":"2025-09-18","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Polymer Degradation and Stability","FirstCategoryId":"92","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S014139102500504X","RegionNum":2,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"POLYMER SCIENCE","Score":null,"Total":0}
引用次数: 0
Abstract
The flame-retardant modification of polymers, while preserving or enhancing their mechanical properties, is critical for engineering plastics. In this study, we develop flame-retardant polycarbonate (PC) composites with improved mechanical performance by incorporating cinnamate-containing liquid crystalline copolyester (CLCP). During the injection molding process, CLCP forms oriented microfibrils in situ, boosting the tensile strength of the composites by up to 66 %. The cinnamate groups in CLCP undergo radical-initiated thermal crosslinking, which increases melt viscosity, prevents dripping, and achieves a UL-94 V-0 rating. The primary flame retardancy mechanism occurs in the condensed phase: early decomposition of CLCP triggers thermal crosslinking, leading to the formation of a dense, graphitized char layer that reduces the peak heat release rate (PHRR) by 46.8 %, total smoke production by 17.9 %, and increases the limiting oxygen index (LOI) to 32.5 % (compared to 27.0 % for neat PC). This dual-functionality of CLCP addresses both the flammability and mechanical limitations of PC, making it a promising candidate for engineering applications requiring high-performance materials. This work introduces a novel molecular design strategy, integrating liquid crystallinity and cinnamate crosslinking, to enhance both flame resistance and mechanical properties in engineering plastics.
期刊介绍:
Polymer Degradation and Stability deals with the degradation reactions and their control which are a major preoccupation of practitioners of the many and diverse aspects of modern polymer technology.
Deteriorative reactions occur during processing, when polymers are subjected to heat, oxygen and mechanical stress, and during the useful life of the materials when oxygen and sunlight are the most important degradative agencies. In more specialised applications, degradation may be induced by high energy radiation, ozone, atmospheric pollutants, mechanical stress, biological action, hydrolysis and many other influences. The mechanisms of these reactions and stabilisation processes must be understood if the technology and application of polymers are to continue to advance. The reporting of investigations of this kind is therefore a major function of this journal.
However there are also new developments in polymer technology in which degradation processes find positive applications. For example, photodegradable plastics are now available, the recycling of polymeric products will become increasingly important, degradation and combustion studies are involved in the definition of the fire hazards which are associated with polymeric materials and the microelectronics industry is vitally dependent upon polymer degradation in the manufacture of its circuitry. Polymer properties may also be improved by processes like curing and grafting, the chemistry of which can be closely related to that which causes physical deterioration in other circumstances.