1-己烯部分取代1-丁烯对线性低密度聚乙烯树脂抗撕裂性和抗慢裂纹扩展性能的影响

Mohammad Hossein Jandaghian, A. Sepahi, S. Hosseini, Romina Esmaeilzade, Ehsan Nikzinat, Ali Salimzadeh, Reza Zaeri, Maryam Masoori
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摘要

摘要:本研究包括利用1-丁烯和1-己烯共聚物的混合物大规模生产薄膜级线性低密度聚乙烯(LLDPE)树脂。目的是评估用1-己烯部分取代1-丁烯对合成树脂的热、物理、机械和流变性能的影响,并将其与以1-丁烯为共聚单体生产的LLDPE对应物并置。尽管对主要物理、热、流变和机械特性的综合研究表明,替代对LLDPE树脂的抗撕裂性和慢裂纹扩展(SCG)弹性都有显著的提高,但通过这些共聚单体的融合而制成的LLDPE树脂的抗撕裂性和慢裂纹扩展(SCG)弹性都有显著的提高。具体来说,该树脂的抗撕裂性和抗SCG性分别表现出超过60%和30%的异常激增。这种明显的增强强调了所提出的技术的可行性,作为增强所需机械性能的有利途径,避免了从1-丁烯到长链α-烯烃共聚物的全面转变。图形抽象
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Tuning tear and slow crack growth resistance of linear low-density polyethylene resins through partial replacement of 1-butene with 1-hexene
Abstract The present study encompasses the utilization of a mixture of 1-butene and 1-hexene comonomers for the large-scale production of a film-grade linear low-density polyethylene (LLDPE) resin. The goal involves assessing the impact stemming from the partial replacement of 1-butene with 1-hexene on the thermal, physical, mechanical and rheological properties of the resultant resin, juxtaposed against an LLDPE counterpart exclusively produced by 1-butene as the comonomer. Although the comprehensive examination of key physical, thermal, rheological and mechanical characteristics indicates nominal influence due to the substitution, a marked escalation materializes in both the tear resistance and slow crack growth (SCG) resilience of the LLDPE resins formulated through the amalgamation of these comonomers. Specifically, the tear and SCG resistance of the proposed resin exhibit an extraordinary surge exceeding 60% and 30%, respectively. This discernible enhancement underscores the viability of the proposed technique as a propitious avenue for augmenting the requisite mechanical properties, obviating the need for an all-encompassing shift from 1-butene to longer-chain α-olefin comonomers. Graphical Abstract
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