Advancing Plastic Recycling: A Review on the Synthesis and Applications of Hierarchical Zeolites in Waste Plastic Hydrocracking

Catalysts Pub Date : 2024-07-12 DOI:10.3390/catal14070450
Muhammad Usman Azam, Waheed Afzal, Inês Graça
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Abstract

The extensive use of plastics has led to a significant environmental threat due to the generation of waste plastic, which has shown significant challenges during recycling. The catalytic hydrocracking route, however, is viewed as a key strategy to manage this fossil-fuel-derived waste into plastic-derived fuels with lower carbon emissions. Despite numerous efforts to identify an effective bi-functional catalyst, especially metal-loaded zeolites, the high-performing zeolite for hydrocracking plastics has yet to be synthesized. This is due to the microporous nature of zeolite, which results in the diffusional limitations of bulkier polymer molecules entering the structure and reducing the overall cracking of plastic and catalyst cycle time. These constraints can be overcome by developing hierarchical zeolites that feature shorter diffusion paths and larger pore sizes, facilitating the movement of bulky polymer molecules. However, if the hierarchical modification process of zeolites is not controlled, it can lead to the synthesis of hierarchical zeolites with compromised functionality or structural integrity, resulting in reduced conversion for the hydrocracking of plastics. Therefore, we provide an overview of various methods for synthesizing hierarchical zeolites, emphasizing significant advancements over the past two decades in developing innovative strategies to introduce additional pore systems. However, the objective of this review is to study the various synthesis approaches based on their effectiveness while developing a clear link between the optimized preparation methods and the structure-activity relationship of the resulting hierarchical zeolites used for the hydrocracking of plastics.
推进塑料回收:分层沸石的合成及其在废塑料加氢裂化中的应用综述
塑料的广泛使用导致了废塑料的产生,对环境造成了严重威胁,而废塑料在回收利用过程中又面临着巨大挑战。然而,催化加氢裂化路线被视为将化石燃料衍生废物转化为碳排放量较低的塑料衍生燃料的关键策略。尽管人们在寻找有效的双功能催化剂,特别是金属负载沸石方面做出了许多努力,但用于加氢裂化塑料的高性能沸石仍有待合成。这是由于沸石具有微孔特性,导致体积较大的聚合物分子进入结构中受到扩散限制,从而降低了塑料的整体裂解率和催化剂的循环时间。这些限制可以通过开发分层沸石来克服,分层沸石具有更短的扩散路径和更大的孔径,有利于大体积聚合物分子的移动。但是,如果不控制沸石的分层改性过程,就会导致合成的分层沸石功能性或结构完整性受损,从而降低塑料加氢裂化的转化率。因此,我们概述了合成分层沸石的各种方法,并强调了过去二十年来在开发创新策略以引入更多孔隙系统方面取得的重大进展。不过,本综述的目的是根据各种合成方法的有效性对其进行研究,同时在优化的制备方法与用于塑料加氢裂化的所得分层沸石的结构-活性关系之间建立明确的联系。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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