Pendant Hydroxy Polyethylene Reactive Additives for Improved Mechanical Properties and Melt Processability of Poly(ethylene terephthalate)/Polyethylene Blends

IF 5.1 1区 化学 Q1 POLYMER SCIENCE
Erin M. Maines, Aristotelis Zografos, Caitlin S. Sample, Aristotle J. Zervoudakis, Theresa M. Reineke, Christopher J. Ellison
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Abstract

Reactive compatibilization is an attractive solution to improve the mechanical properties of polymer blends that inherently result from plastic recycling processes. In this study, pendant hydroxy polyethylene reactive additives were synthesized through ring-opening metathesis polymerization (ROMP) and their ability to compatibilize poly(ethylene terephthalate) (PET)/polyethylene blends through reactive compatibilization was evaluated. The ROMP synthesis strategy enabled the deconvolution of the effects of overall number-average molar mass (Mn) and average molar mass between reactive hydroxy groups (Mg) on compatibilization effectiveness. The results of this study suggest a near-optimal Mg ∼ 1 kg/mol where the strain at break (εb) of the blend with 1 wt % additive is increased significantly (εb ∼ 280%) over the neat blend without the additive (εb ∼ 16%), independent of Mn. Near-optimal Mg additives were effective at industrially relevant reaction times of 5–10 min, at loadings as low as 0.5 wt %, and in blends containing one of two different types of PET, suggesting their versatility and commercial applicability. Extensional viscosity was characterized and melt strain hardening (MSH) was observed to be highly dependent on the viscosity ratio between the matrix and dispersed phases, which is a function of temperature. When MSH is present, we show that reactive compatibilizers capable of forming branched reaction products offer an improvement to the MSH, compared to linear analogues. These findings suggest that branched compatibilizers may be advantageous for melt processability of compatibilized recyclates in processes dominated by strong extensional flows, such as film blowing, foaming, and thermoforming.

Abstract Image

用于改善聚对苯二甲酸乙二酯/聚乙烯混合物机械性能和熔融加工性的羟基聚乙烯反应添加剂
反应性相容是一种极具吸引力的解决方案,可改善塑料回收过程中固有的聚合物混合物的机械性能。本研究通过开环偏聚(ROMP)合成了垂羟基聚乙烯反应性添加剂,并评估了它们通过反应性相容来相容聚对苯二甲酸乙二酯(PET)/聚乙烯混合物的能力。采用 ROMP 合成策略,可以消除总的平均摩尔质量(Mn)和反应性羟基之间的平均摩尔质量(Mg)对相容效果的影响。研究结果表明,在 Mg ∼ 1 kg/mol 接近最佳值时,添加 1 wt % 添加剂的混合物的断裂应变(εb)比未添加添加剂的纯混合物(εb ∼ 16%)显著增加(εb ∼ 280%),且与 Mn 无关。接近最佳的镁添加剂在工业相关的 5-10 分钟反应时间、低至 0.5 wt % 的添加量以及含有两种不同类型 PET 的混合物中均有效,这表明它们具有多功能性和商业适用性。对延伸粘度进行了表征,发现熔体应变硬化(MSH)与基体和分散相之间的粘度比密切相关,而粘度比是温度的函数。当出现 MSH 时,我们发现与线性类似物相比,能够形成支化反应产物的活性相容剂可改善 MSH。这些研究结果表明,在吹膜、发泡和热成型等以强延伸流为主的加工过程中,支化相容剂可能对相容回收物的熔融加工性有利。
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来源期刊
Macromolecules
Macromolecules 工程技术-高分子科学
CiteScore
9.30
自引率
16.40%
发文量
942
审稿时长
2 months
期刊介绍: Macromolecules publishes original, fundamental, and impactful research on all aspects of polymer science. Topics of interest include synthesis (e.g., controlled polymerizations, polymerization catalysis, post polymerization modification, new monomer structures and polymer architectures, and polymerization mechanisms/kinetics analysis); phase behavior, thermodynamics, dynamic, and ordering/disordering phenomena (e.g., self-assembly, gelation, crystallization, solution/melt/solid-state characteristics); structure and properties (e.g., mechanical and rheological properties, surface/interfacial characteristics, electronic and transport properties); new state of the art characterization (e.g., spectroscopy, scattering, microscopy, rheology), simulation (e.g., Monte Carlo, molecular dynamics, multi-scale/coarse-grained modeling), and theoretical methods. Renewable/sustainable polymers, polymer networks, responsive polymers, electro-, magneto- and opto-active macromolecules, inorganic polymers, charge-transporting polymers (ion-containing, semiconducting, and conducting), nanostructured polymers, and polymer composites are also of interest. Typical papers published in Macromolecules showcase important and innovative concepts, experimental methods/observations, and theoretical/computational approaches that demonstrate a fundamental advance in the understanding of polymers.
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