Pore-Structure Engineering of Hierarchical β Zeolites for the Enhanced Hydrocracking of Waste Plastics to Liquid Fuels

IF 11.3 1区 化学 Q1 CHEMISTRY, PHYSICAL ACS Catalysis Pub Date : 2024-10-17 DOI:10.1021/acscatal.4c0535410.1021/acscatal.4c05354
Muhammad Usman Azam, Auguste Fernandes, Maria João Ferreira, Waheed Afzal* and Inês Graça*, 
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Abstract

Hydrocracking of plastics over bifunctional hierarchical zeolites is promising for the upcycling of plastics into value-added products. However, the exact role of their acidic and textural properties toward the catalytic activity remains unclear. Herein, we modified the structure of a β zeolite via dealumination and desilication routes, resulting in hierarchical zeolites. The parent and hierarchical modified β zeolite samples were loaded with Ni and studied for the hydrocracking of virgin HDPE. In comparison to the parent and dealuminated β zeolite, desilicated β zeolite showed a higher conversion of 87.8% with 66.7% of the products in the gasoline range, owing to its significantly high textural properties. The conversion and selectivity of gasoline-range hydrocarbons over the desilicated zeolite were further improved to 95.9 and 69.2%, respectively, by Ni addition. To unlock the structure–activity correlation of the various zeolite samples, the role of different activity-driven factors was studied, resulting in an empirical relationship that aligns with the observed conversions over different zeolite samples. Moreover, it was observed that it is possible to achieve high selectivity of iso-paraffins in gasoline-range hydrocarbons via the optimization of the balance between metal-acid sites on bifunctional hierarchical zeolites. Furthermore, both Ni-loaded hierarchical β zeolites showed good stability and the ability to be regenerated under cyclic runs. The best-performing Ni-loaded desilicated β zeolite was also maintained over various postconsumer waste plastics (conversion = 85–95%) and when using a mixture of postconsumer waste plastics (88.4%). A life cycle assessment and a comparison with the recent literature also demonstrated the advantages of the proposed hierarchical modification routes in achieving high gasoline productivity (6.6–7.6 ggasoline/gcat·h) and less environmental impact. Overall, these findings highlight the role of improved textural properties of noble-metal-free, easily modifiable, and environmentally friendly bifunctional hierarchical β zeolites for the enhanced conversion of waste plastics into liquid fuels.

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用于将废塑料加氢裂化为液体燃料的分层 β 沸石孔隙结构工程研究
在双功能分层沸石上对塑料进行加氢裂化有望将塑料转化为高附加值产品。然而,它们的酸性和质地特性对催化活性的确切作用仍不清楚。在此,我们通过脱铝和脱硅的方法对β沸石的结构进行了改性,从而得到了分层沸石。在母体和分层改性的β沸石样品中添加了镍,并对原生高密度聚乙烯的加氢裂化进行了研究。与母体和脱铝 β 沸石相比,脱硅 β 沸石的转化率更高,达到 87.8%,其中 66.7% 的产物在汽油范围内,这是因为它具有显著的高质地特性。通过添加镍,脱硅沸石的汽油范围烃类转化率和选择性进一步提高,分别达到 95.9% 和 69.2%。为了解开不同沸石样品的结构-活性相关性,对不同活性驱动因素的作用进行了研究,得出了与不同沸石样品上观察到的转化率相一致的经验关系。此外,研究还发现,通过优化双功能分层沸石上金属-酸位点之间的平衡,有可能在汽油范围的碳氢化合物中实现异链烷烃的高选择性。此外,两种镍负载分层β沸石都表现出良好的稳定性和循环再生能力。在使用各种消费后废塑料(转化率 = 85-95%)和消费后废塑料混合物(88.4%)时,镍负载脱硅 β 沸石也能保持最佳性能。生命周期评估以及与近期文献的比较也表明,所建议的分层改性路线在实现高汽油生产率(6.6-7.6 ggasoline/gcat-h)和减少环境影响方面具有优势。总之,这些研究结果凸显了不含惰性金属、易于改性且环保的双功能分层 β 沸石在提高废塑料转化为液体燃料的质构特性方面的作用。
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来源期刊
ACS Catalysis
ACS Catalysis CHEMISTRY, PHYSICAL-
CiteScore
20.80
自引率
6.20%
发文量
1253
审稿时长
1.5 months
期刊介绍: ACS Catalysis is an esteemed journal that publishes original research in the fields of heterogeneous catalysis, molecular catalysis, and biocatalysis. It offers broad coverage across diverse areas such as life sciences, organometallics and synthesis, photochemistry and electrochemistry, drug discovery and synthesis, materials science, environmental protection, polymer discovery and synthesis, and energy and fuels. The scope of the journal is to showcase innovative work in various aspects of catalysis. This includes new reactions and novel synthetic approaches utilizing known catalysts, the discovery or modification of new catalysts, elucidation of catalytic mechanisms through cutting-edge investigations, practical enhancements of existing processes, as well as conceptual advances in the field. Contributions to ACS Catalysis can encompass both experimental and theoretical research focused on catalytic molecules, macromolecules, and materials that exhibit catalytic turnover.
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