Loren C. Brown , Cole R. Davis , Andrew T. Kerr , Matthew Laskoski
{"title":"杂环自固化邻苯二腈树脂","authors":"Loren C. Brown , Cole R. Davis , Andrew T. Kerr , Matthew Laskoski","doi":"10.1016/j.reactfunctpolym.2025.106383","DOIUrl":null,"url":null,"abstract":"<div><div>A new class of self-curing phthalonitrile (PN) resins composed of various heterocycles is detailed. The heterocyclic-imine PN (HIPN) resins were synthesized utilizing methanol at ambient temperature and polar aprotic solvents acetone or dimethyl sulfoxide. Characterization of the resins was conducted via proton (<sup>1</sup>H) and carbon (<sup>13</sup>C) nuclear magnetic resonance (NMR) spectroscopy, differential scanning calorimetry (DSC), thermogravimetric analysis (TGA), mechanical analysis (torsion), single crystal X-ray diffraction (SCXRD), and rheometry. The HIPN resins were self-curing due to the heterocycle, imine, and PN moieties present and displayed a range of viscosities from 146 to 1295 cP at 200 °C. The resulting HIPN polymers were prepared by post-curing to 380 °C and exhibited excellent thermal stability up to a 76 % char yield at 1000 °C. The cured HIPN polymers displayed improved mechanical performance in comparison to rival PN systems with storage moduli near 1600 MPa. This combination of properties suggests the HIPN resins are excellent materials for thermomechanical applications.</div></div>","PeriodicalId":20916,"journal":{"name":"Reactive & Functional Polymers","volume":"215 ","pages":"Article 106383"},"PeriodicalIF":5.1000,"publicationDate":"2025-06-23","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Heterocyclic self-curing phthalonitrile resins\",\"authors\":\"Loren C. Brown , Cole R. Davis , Andrew T. Kerr , Matthew Laskoski\",\"doi\":\"10.1016/j.reactfunctpolym.2025.106383\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><div>A new class of self-curing phthalonitrile (PN) resins composed of various heterocycles is detailed. The heterocyclic-imine PN (HIPN) resins were synthesized utilizing methanol at ambient temperature and polar aprotic solvents acetone or dimethyl sulfoxide. Characterization of the resins was conducted via proton (<sup>1</sup>H) and carbon (<sup>13</sup>C) nuclear magnetic resonance (NMR) spectroscopy, differential scanning calorimetry (DSC), thermogravimetric analysis (TGA), mechanical analysis (torsion), single crystal X-ray diffraction (SCXRD), and rheometry. The HIPN resins were self-curing due to the heterocycle, imine, and PN moieties present and displayed a range of viscosities from 146 to 1295 cP at 200 °C. The resulting HIPN polymers were prepared by post-curing to 380 °C and exhibited excellent thermal stability up to a 76 % char yield at 1000 °C. The cured HIPN polymers displayed improved mechanical performance in comparison to rival PN systems with storage moduli near 1600 MPa. This combination of properties suggests the HIPN resins are excellent materials for thermomechanical applications.</div></div>\",\"PeriodicalId\":20916,\"journal\":{\"name\":\"Reactive & Functional Polymers\",\"volume\":\"215 \",\"pages\":\"Article 106383\"},\"PeriodicalIF\":5.1000,\"publicationDate\":\"2025-06-23\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Reactive & Functional Polymers\",\"FirstCategoryId\":\"5\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S1381514825002354\",\"RegionNum\":3,\"RegionCategory\":\"工程技术\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"CHEMISTRY, APPLIED\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Reactive & Functional Polymers","FirstCategoryId":"5","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S1381514825002354","RegionNum":3,"RegionCategory":"工程技术","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"CHEMISTRY, APPLIED","Score":null,"Total":0}
A new class of self-curing phthalonitrile (PN) resins composed of various heterocycles is detailed. The heterocyclic-imine PN (HIPN) resins were synthesized utilizing methanol at ambient temperature and polar aprotic solvents acetone or dimethyl sulfoxide. Characterization of the resins was conducted via proton (1H) and carbon (13C) nuclear magnetic resonance (NMR) spectroscopy, differential scanning calorimetry (DSC), thermogravimetric analysis (TGA), mechanical analysis (torsion), single crystal X-ray diffraction (SCXRD), and rheometry. The HIPN resins were self-curing due to the heterocycle, imine, and PN moieties present and displayed a range of viscosities from 146 to 1295 cP at 200 °C. The resulting HIPN polymers were prepared by post-curing to 380 °C and exhibited excellent thermal stability up to a 76 % char yield at 1000 °C. The cured HIPN polymers displayed improved mechanical performance in comparison to rival PN systems with storage moduli near 1600 MPa. This combination of properties suggests the HIPN resins are excellent materials for thermomechanical applications.
期刊介绍:
Reactive & Functional Polymers provides a forum to disseminate original ideas, concepts and developments in the science and technology of polymers with functional groups, which impart specific chemical reactivity or physical, chemical, structural, biological, and pharmacological functionality. The scope covers organic polymers, acting for instance as reagents, catalysts, templates, ion-exchangers, selective sorbents, chelating or antimicrobial agents, drug carriers, sensors, membranes, and hydrogels. This also includes reactive cross-linkable prepolymers and high-performance thermosetting polymers, natural or degradable polymers, conducting polymers, and porous polymers.
Original research articles must contain thorough molecular and material characterization data on synthesis of the above polymers in combination with their applications. Applications include but are not limited to catalysis, water or effluent treatment, separations and recovery, electronics and information storage, energy conversion, encapsulation, or adhesion.