{"title":"Structural regulation of TLCP and evaluation of its long-term heat resistance after solid-state polymerization","authors":"Boang He, Ke Ma, Hai Wan, Ying Wang, Yuhan Chen, Wei Liu, Yuan Liang, Wenbin Jin, Shuohan Huang, Yong He, Yanping Wang, Yumin Xia","doi":"10.1016/j.polymdegradstab.2025.111405","DOIUrl":null,"url":null,"abstract":"<div><div>In this paper, a series of liquid crystal polyarylates were synthesized through a two-step method involving p-hydroxybenzoic acid (HBA), 4,4′-biphenyldiol (BP), terephthalic acid (TA), and isophthalic acid (IA). By adjusting the IA content (0–5 mol%), it was found that the introduction of IA significantly reduced the melting point (T<sub>m</sub>) and crystallinity of the polyarylate while retaining its liquid crystallinity. When the IA content was 3 mol%, the polyarylate exhibited both optimized processability (T<sub>m</sub> = 282.7 °C) and thermal stability (T<sub>5 %</sub> > 360 °C). The polymerization process was further optimized, and solid-state polymerization (SSP) was employed to increase the molecular weight. The results demonstrated that under solid-state polymerization conditions of either 270 °C for 6 h or 280 °C for 3 h, the polyarylate achieved a tensile strength exceeding 100 MPa and a softening temperature above 300 °C. Using the stepwise isothermal method (SIM), the long-term performance of the polyarylate at elevated temperatures was predicted. The solid-state polymerized polyarylate showed a significant reduction in strain under a constant stress at 170 °C over 10 years, confirming its long-term thermal stability. This study provides a novel strategy for the structural design and performance optimization of high-temperature-resistant engineering plastics.</div></div>","PeriodicalId":406,"journal":{"name":"Polymer Degradation and Stability","volume":"239 ","pages":"Article 111405"},"PeriodicalIF":6.3000,"publicationDate":"2025-05-02","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/S0141391025002344","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
In this paper, a series of liquid crystal polyarylates were synthesized through a two-step method involving p-hydroxybenzoic acid (HBA), 4,4′-biphenyldiol (BP), terephthalic acid (TA), and isophthalic acid (IA). By adjusting the IA content (0–5 mol%), it was found that the introduction of IA significantly reduced the melting point (Tm) and crystallinity of the polyarylate while retaining its liquid crystallinity. When the IA content was 3 mol%, the polyarylate exhibited both optimized processability (Tm = 282.7 °C) and thermal stability (T5 % > 360 °C). The polymerization process was further optimized, and solid-state polymerization (SSP) was employed to increase the molecular weight. The results demonstrated that under solid-state polymerization conditions of either 270 °C for 6 h or 280 °C for 3 h, the polyarylate achieved a tensile strength exceeding 100 MPa and a softening temperature above 300 °C. Using the stepwise isothermal method (SIM), the long-term performance of the polyarylate at elevated temperatures was predicted. The solid-state polymerized polyarylate showed a significant reduction in strain under a constant stress at 170 °C over 10 years, confirming its long-term thermal stability. This study provides a novel strategy for the structural design and performance optimization of high-temperature-resistant 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.