{"title":"增强机械性能的耐用阻燃再生纤维素纤维的制备","authors":"Guangming Sun, Jieyu Wei, Hejun Li, Tian Li, Hui Xu, Fayu Sun, Guangxian Zhang","doi":"10.1016/j.polymdegradstab.2025.111523","DOIUrl":null,"url":null,"abstract":"<div><div>The incorporation of flame retardants into regenerated cellulose spinning solutions is a crucial approach for producing flame-retardant regenerated cellulose fibers. However, this method often encounters challenges such as poor compatibility and inadequate dispersion of the flame retardants within the matrix. In this study, a novel flame retardant (P-TSDPAH) was synthesized using ordinary materials such as tetramethylphosphonium sulfate, dimethyl phosphite, and ammonia solution. The P-TSDPAH contains a lot of -NH- bonds, exhibits compatibility with cellulose and N-methylmorpholine N-oxide (NMMO), and remains good dispersion in the cellulose spinning solution. SEM analysis revealed that the P-TSDPAH was uniformly distributed within the FR-fiber 15 % without aggregation, and EDS results confirmed the presence of substantial phosphorus content. FTIR analysis confirmed the presence of characteristic P-C-O, C<img>N, and N<img>H structures within the FR-fiber 15 %. XRD analysis revealed an enhanced crystallinity in the FR-fiber 15 % upon incorporation of the P-TSDPAH. Compared with pure regenerated cellulose fibers, the peak heat release rate and total heat release of FR-fiber 15 % were reduced by 88.61 % and 30.50 %, respectively, while the char residue at 700 °C increased by 142.79 %. TG and TG-IR analyses demonstrated the flame retardancy of the FR-fiber 15 %, revealing condensed-phase flame retardant mechanism, while limiting oxygen index (LOI) remained at 35.0 % even after 50 washing cycles (NFPA 2112–2012 standard), demonstrating durable performance. Additionally, the incorporation of the P-TSDPAH enhanced the mechanical properties of the regenerated cellulose fibers, which the relative breaking strength and elongation increased by 31.16 % and 48.05 %, respectively. Therefore, the synthesized P-TSDPAH demonstrates application potential for developing durable flame-retardant regenerated cellulose fibers.</div></div>","PeriodicalId":406,"journal":{"name":"Polymer Degradation and Stability","volume":"241 ","pages":"Article 111523"},"PeriodicalIF":7.4000,"publicationDate":"2025-07-02","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Preparation of a durable flame-retardant regenerated cellulose fiber with enhanced mechanical properties\",\"authors\":\"Guangming Sun, Jieyu Wei, Hejun Li, Tian Li, Hui Xu, Fayu Sun, Guangxian Zhang\",\"doi\":\"10.1016/j.polymdegradstab.2025.111523\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><div>The incorporation of flame retardants into regenerated cellulose spinning solutions is a crucial approach for producing flame-retardant regenerated cellulose fibers. However, this method often encounters challenges such as poor compatibility and inadequate dispersion of the flame retardants within the matrix. In this study, a novel flame retardant (P-TSDPAH) was synthesized using ordinary materials such as tetramethylphosphonium sulfate, dimethyl phosphite, and ammonia solution. The P-TSDPAH contains a lot of -NH- bonds, exhibits compatibility with cellulose and N-methylmorpholine N-oxide (NMMO), and remains good dispersion in the cellulose spinning solution. SEM analysis revealed that the P-TSDPAH was uniformly distributed within the FR-fiber 15 % without aggregation, and EDS results confirmed the presence of substantial phosphorus content. FTIR analysis confirmed the presence of characteristic P-C-O, C<img>N, and N<img>H structures within the FR-fiber 15 %. XRD analysis revealed an enhanced crystallinity in the FR-fiber 15 % upon incorporation of the P-TSDPAH. Compared with pure regenerated cellulose fibers, the peak heat release rate and total heat release of FR-fiber 15 % were reduced by 88.61 % and 30.50 %, respectively, while the char residue at 700 °C increased by 142.79 %. TG and TG-IR analyses demonstrated the flame retardancy of the FR-fiber 15 %, revealing condensed-phase flame retardant mechanism, while limiting oxygen index (LOI) remained at 35.0 % even after 50 washing cycles (NFPA 2112–2012 standard), demonstrating durable performance. Additionally, the incorporation of the P-TSDPAH enhanced the mechanical properties of the regenerated cellulose fibers, which the relative breaking strength and elongation increased by 31.16 % and 48.05 %, respectively. Therefore, the synthesized P-TSDPAH demonstrates application potential for developing durable flame-retardant regenerated cellulose fibers.</div></div>\",\"PeriodicalId\":406,\"journal\":{\"name\":\"Polymer Degradation and Stability\",\"volume\":\"241 \",\"pages\":\"Article 111523\"},\"PeriodicalIF\":7.4000,\"publicationDate\":\"2025-07-02\",\"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/S0141391025003520\",\"RegionNum\":2,\"RegionCategory\":\"化学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"POLYMER SCIENCE\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Polymer Degradation and Stability","FirstCategoryId":"92","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S0141391025003520","RegionNum":2,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"POLYMER SCIENCE","Score":null,"Total":0}
Preparation of a durable flame-retardant regenerated cellulose fiber with enhanced mechanical properties
The incorporation of flame retardants into regenerated cellulose spinning solutions is a crucial approach for producing flame-retardant regenerated cellulose fibers. However, this method often encounters challenges such as poor compatibility and inadequate dispersion of the flame retardants within the matrix. In this study, a novel flame retardant (P-TSDPAH) was synthesized using ordinary materials such as tetramethylphosphonium sulfate, dimethyl phosphite, and ammonia solution. The P-TSDPAH contains a lot of -NH- bonds, exhibits compatibility with cellulose and N-methylmorpholine N-oxide (NMMO), and remains good dispersion in the cellulose spinning solution. SEM analysis revealed that the P-TSDPAH was uniformly distributed within the FR-fiber 15 % without aggregation, and EDS results confirmed the presence of substantial phosphorus content. FTIR analysis confirmed the presence of characteristic P-C-O, CN, and NH structures within the FR-fiber 15 %. XRD analysis revealed an enhanced crystallinity in the FR-fiber 15 % upon incorporation of the P-TSDPAH. Compared with pure regenerated cellulose fibers, the peak heat release rate and total heat release of FR-fiber 15 % were reduced by 88.61 % and 30.50 %, respectively, while the char residue at 700 °C increased by 142.79 %. TG and TG-IR analyses demonstrated the flame retardancy of the FR-fiber 15 %, revealing condensed-phase flame retardant mechanism, while limiting oxygen index (LOI) remained at 35.0 % even after 50 washing cycles (NFPA 2112–2012 standard), demonstrating durable performance. Additionally, the incorporation of the P-TSDPAH enhanced the mechanical properties of the regenerated cellulose fibers, which the relative breaking strength and elongation increased by 31.16 % and 48.05 %, respectively. Therefore, the synthesized P-TSDPAH demonstrates application potential for developing durable flame-retardant regenerated cellulose fibers.
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.