Melt blending of commercial linear polyethylene with low-entangled ultra-high molecular weight polyethylene: From dispersion compatibility to viscoelastic scaling laws

IF 4.1 2区 化学 Q2 POLYMER SCIENCE
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Abstract

This study investigates the dispersion and compatibility of low-entangled “dis-entangled” UHMWPE (dis-UH) in a high-density polyethylene (HDPE) matrix using solvent-free melt-blending conditions and compares it with entangled UHMWPE (eUH) in the same matrix. The findings reveal that dis-UH/HDPE exhibits a significantly lower viscosity ratio than eUH/HDPE (1 and 4, respectively), indicating a lower critical capillary number (Cacritical), thus enhanced dispersion and compatibility. Blends with varying dis-UH content up to 20 wt% show homogeneity, evidenced by DSC and SEM analysis, and demonstrate improved mechanical properties by 36 % in the maximum stress (σmax) and 39 % in Young's modulus (E). Linear viscoelasticity assessments reveal that higher dis-UH content slow the dynamics and increase the apparent weight average molecular weight (Mw), consistent with previous reports for linear entangled PE. The zero-shear viscosity (η0) scaling with Mw (η0 M n) is adjusted for high polydispersity, yielding a transitional point in the scaling exponent (n) from 3.6 to 3 at a reptation number of entanglement segments (Mr/Me) of ∼287, in line with theoretical predictions. To rationalize the success of the homogenization process, we propose a qualitative molecular picture inspired from the constraint release Rouse mechanism involved in the disorientation process of bi-disperse linear polymers. In the case of dis-UH/HDPE blends, with initially lower density of long-long entanglements within dis-UH, and the highest density of short-short entanglements within HDPE matrix, the formation of long-short entanglements between dis-UH and HDPE is facilitated, which results in successful homogenization process. In the contrary, the establishment of long-short entanglements in eUH/HDPE blends will require unwinding of the long-long entanglements, which holds a higher kinetic barrier compared to dis-UH/HDPE blends, leading to unsuccessful homogenization.

Abstract Image

商用线性聚乙烯与低缠结超高分子量聚乙烯的熔融共混:从分散相容性到粘弹性缩放定律
本研究采用无溶剂熔融混合条件,研究了低缠结超高分子量聚乙烯(dis-UH)在高密度聚乙烯(HDPE)基体中的分散性和相容性,并与相同基体中的缠结超高分子量聚乙烯(eUH)进行了比较。研究结果表明,dis-UH/HDPE 的粘度比(分别为 1 和 4)明显低于 eUH/HDPE,这表明临界毛细管数(Cacritical)更低,从而提高了分散性和相容性。DSC 和 SEM 分析表明,dis-UH 含量最高为 20 wt% 的混合物具有均匀性,最大应力 (σmax) 和杨氏模量 (E) 分别提高了 36% 和 39%。线性粘弹性评估结果表明,Dis-UH 含量越高,动态变化越慢,表观平均分子量(Mw)越大,这与之前关于线性缠结聚乙烯的报告一致。零剪切粘度(η0)与 Mw 的比例(η0 ∝ M n)随高多分散性而调整,在纠缠段数(Mr/Me)为 287 时,比例指数(n)从 3.6 到 3 的过渡点,与理论预测一致。为了合理解释均质化过程的成功,我们从双分散线性聚合物失向过程中涉及的约束释放劳斯机制中获得启发,提出了一种定性分子图谱。在二硫化氢/高密度聚乙烯共混物中,二硫化氢内部的长-长缠结密度最初较低,而高密度聚乙烯基体内部的短-短缠结密度最高,这就促进了二硫化氢和高密度聚乙烯之间长-短缠结的形成,从而成功实现了均质化过程。相反,在 eUH/HDPE 混合物中建立长短缠结需要解开长长缠结,这与 dis-UH/HDPE 混合物相比具有更高的动力学障碍,从而导致均化不成功。
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来源期刊
Polymer
Polymer 化学-高分子科学
CiteScore
7.90
自引率
8.70%
发文量
959
审稿时长
32 days
期刊介绍: Polymer is an interdisciplinary journal dedicated to publishing innovative and significant advances in Polymer Physics, Chemistry and Technology. We welcome submissions on polymer hybrids, nanocomposites, characterisation and self-assembly. Polymer also publishes work on the technological application of polymers in energy and optoelectronics. The main scope is covered but not limited to the following core areas: Polymer Materials Nanocomposites and hybrid nanomaterials Polymer blends, films, fibres, networks and porous materials Physical Characterization Characterisation, modelling and simulation* of molecular and materials properties in bulk, solution, and thin films Polymer Engineering Advanced multiscale processing methods Polymer Synthesis, Modification and Self-assembly Including designer polymer architectures, mechanisms and kinetics, and supramolecular polymerization Technological Applications Polymers for energy generation and storage Polymer membranes for separation technology Polymers for opto- and microelectronics.
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