High-Temperature Size Exclusion Chromatography for Advanced Recycling: Systematic Errors in Analysis of Polyethylene─Alkane Mixtures

IF 4.7 2区 化学 Q2 MATERIALS SCIENCE, MULTIDISCIPLINARY
Mason D. Jones, Christine W. Barker, Fawaz Motolani, Rakesh Patter, S. Michael Kilbey II., Bert D. Chandler, Brian K. Long* and Bryan D. Vogt*, 
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Abstract

Polyolefins, which dominate the plastics marketplace, require high-temperature size exclusion chromatography (HT-SEC) to characterize their molar masses. Chemical recycling methods designed to deconstruct plastic waste into smaller molecules (i.e., depolymerization methods) rely on HT-SEC to characterize their products, but depolymerization methods often yield a complex mixture, including components below the typical separation range of commercial HT-SEC columns. Herein, we report the accuracy and limitations of triple detection HT-SEC to analyze model chemical recycling products. We examined the chromatographic separation and quantification of individual components and mixtures of short polyethylenes (apparent Mn = 465 and 2722 g/mol), hexatriacontane (C36H74, M = 507 g/mol), dotriacontane (C32H66, M = 451 g/mol), and octadecane (C18H38, M = 254 g/mol). Despite short alkanes exhibiting molar masses below the lower molar mass limit of the columns (500 g/mol), the separation of their mixtures was resolved via refractive index (RI) detection. However, the determined molar masses of these alkane mixtures did not agree with the known molar masses of the short alkanes or their prepared mixtures. Similarly, the SEC analysis of mixtures containing discrete alkanes with low molar mass PE revealed that their individual components are easily resolved in the HT-SEC chromatogram. No obvious shift in the elution volume of the blend components versus the elution volume of the pure components was observed. However, inaccurate molar masses and molar mass distributions for these alkane-PE mixtures are calculated from the HT-SEC data. These inaccuracies are attributable to two factors: (1) molar mass-dependent ∂n/∂c for low molar mass components and (2) the small size of the molecules in solution that limits light scattering. These results highlight the importance of considering measurement limitations for quantitative interpretation of triple detection HT-SEC data obtained from chemical recycling and depolymerization experiments that commonly contain complex mixtures of polymeric, oligomeric, and small molecule alkanes.

用于高级回收的高温粒径排除色谱法:分析聚乙烯-烷烃混合物的系统误差
聚烯烃,主导塑料市场,需要高温尺寸排除色谱(HT-SEC)表征其摩尔质量。旨在将塑料垃圾分解成小分子的化学回收方法(即解聚方法)依赖HT-SEC来表征其产品,但解聚方法通常会产生复杂的混合物,包括低于商用HT-SEC柱典型分离范围的成分。在此,我们报告了三重检测HT-SEC分析模型化学回收产品的准确性和局限性。我们考察了短聚乙烯(表观Mn = 465和2722 g/mol)、六正辛烷(C36H74, M = 507 g/mol)、多正辛烷(C32H66, M = 451 g/mol)和十八正辛烷(C18H38, M = 254 g/mol)的单个组分和混合物的色谱分离和定量。尽管短链烷烃的摩尔质量低于色谱柱的摩尔质量下限(500 g/mol),但它们的混合物的分离是通过折射率(RI)检测解决的。然而,测定的这些烷烃混合物的摩尔质量与已知的短烷烃或其制备的混合物的摩尔质量不一致。同样,对含有低摩尔质量PE的离散烷烃混合物的SEC分析表明,它们的单个组分在HT-SEC色谱图中很容易被分解。混合组分的洗脱体积与纯组分的洗脱体积没有明显的变化。然而,这些烷烃-聚乙烯混合物的摩尔质量和摩尔质量分布是由HT-SEC数据计算出来的。这些不准确性可归因于两个因素:(1)低摩尔质量组分的与摩尔质量相关的∂n/∂c;(2)溶液中分子的小尺寸限制了光散射。这些结果强调了考虑定量解释从化学回收和解聚实验中获得的三重检测HT-SEC数据的测量局限性的重要性,这些数据通常包含聚合物,低聚物和小分子烷烃的复杂混合物。
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来源期刊
CiteScore
7.20
自引率
6.00%
发文量
810
期刊介绍: ACS Applied Polymer Materials is an interdisciplinary journal publishing original research covering all aspects of engineering, chemistry, physics, and biology relevant to applications of polymers. The journal is devoted to reports of new and original experimental and theoretical research of an applied nature that integrates fundamental knowledge in the areas of materials, engineering, physics, bioscience, polymer science and chemistry into important polymer applications. The journal is specifically interested in work that addresses relationships among structure, processing, morphology, chemistry, properties, and function as well as work that provide insights into mechanisms critical to the performance of the polymer for applications.
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