{"title":"Enhanced stabilisation performance of HDPE via siloxane bonded ZnO with phenolic antioxidants","authors":"Jianglai Ai , Yuying Zheng , Jie Zhang","doi":"10.1016/j.polymdegradstab.2025.111276","DOIUrl":null,"url":null,"abstract":"<div><div>The poor resistance of high-density polyethylene (HDPE) to thermal-oxidative aging and ultraviolet (UV) degradation significantly limits its service life. In this study, the nanocomposite ZnO-AO was synthesized using γ-glycidoxypropyltrimethoxysilane (GPTMS) as a bridging agent, which facilitated the loading of a significant quantity of the hindered phenolic antioxidant (AO) onto the surface of ZnO nanoparticles, and the HDPE/ZnO-AO composites were subsequently prepared by melt blending. The results indicated that the combination of ZnO and AO was synergistic, and the more optimized para-substituent structure of AO significantly reduced the hydroxyl bond dissociation energy (BDE) of the hindered phenols, thereby enhancing antioxidant activity. Additionally, the hydroxyl groups on the surface of ZnO were substituted with AO, which improved the particle dispersion. After 400 h of UV aging, HDPE/ZnO-AO retained 78.36 % and 95.92 % of its elongation at break and impact strength, respectively, compared to only 2.25 % and 6.17 % for pure HDPE. After 28 days of thermal-oxidative aging, the carbonyl index of HDPE/ZnO-AO increased by only 0.18, significantly lower than that of HDPE (0.43). Accordingly, the ZnO and AO, covalently linked by GPTMS, demonstrated enhanced performance compared to individual original capabilities, successfully integrating efficient thermal-oxidative stability and UV protection. This study provides a promising approach for the development of long-lasting HDPE composites.</div></div>","PeriodicalId":406,"journal":{"name":"Polymer Degradation and Stability","volume":"236 ","pages":"Article 111276"},"PeriodicalIF":6.3000,"publicationDate":"2025-02-21","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/S0141391025001065","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 poor resistance of high-density polyethylene (HDPE) to thermal-oxidative aging and ultraviolet (UV) degradation significantly limits its service life. In this study, the nanocomposite ZnO-AO was synthesized using γ-glycidoxypropyltrimethoxysilane (GPTMS) as a bridging agent, which facilitated the loading of a significant quantity of the hindered phenolic antioxidant (AO) onto the surface of ZnO nanoparticles, and the HDPE/ZnO-AO composites were subsequently prepared by melt blending. The results indicated that the combination of ZnO and AO was synergistic, and the more optimized para-substituent structure of AO significantly reduced the hydroxyl bond dissociation energy (BDE) of the hindered phenols, thereby enhancing antioxidant activity. Additionally, the hydroxyl groups on the surface of ZnO were substituted with AO, which improved the particle dispersion. After 400 h of UV aging, HDPE/ZnO-AO retained 78.36 % and 95.92 % of its elongation at break and impact strength, respectively, compared to only 2.25 % and 6.17 % for pure HDPE. After 28 days of thermal-oxidative aging, the carbonyl index of HDPE/ZnO-AO increased by only 0.18, significantly lower than that of HDPE (0.43). Accordingly, the ZnO and AO, covalently linked by GPTMS, demonstrated enhanced performance compared to individual original capabilities, successfully integrating efficient thermal-oxidative stability and UV protection. This study provides a promising approach for the development of long-lasting HDPE composites.
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.