使用Ru/Al2O3催化剂†从聚乙烯塑料中有效生产液体/蜡燃料

EES catalysis Pub Date : 2025-04-26 DOI:10.1039/D5EY00070J
Jueun Kim, Donghyeon Kim, Byung Gwan Park, Daewon Oh, Shinjae Lee, Jihun Kim, Eonu Nam and Kwangjin An
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引用次数: 0

摘要

氢解为将聚烯烃塑料转化为有价值的液体和蜡燃料提供了一条有前途的途径。这个过程包括脱氢、C-C键裂解和催化剂活性金属位点的加氢。控制这些金属位点的性质是优化整体反应活性的关键。在这项研究中,钌催化剂负载在纳米片组装的Al2O3 (NA-Al2O3)上用于氢解聚乙烯(PE)。与商用Al2O3不同,NA-Al2O3促进Ru-Al键的形成,导致更强的金属支撑相互作用。在相同的Ru负载下,这些增强的相互作用导致NA-Al2O3表面上Ru的分散性更高,Ru的种类更少。为了研究Ru负载的影响,合成了一系列催化剂(xRu/NA-Al2O3, x = 0.5, 1, 5和8 wt% Ru),发现Ru的粒径和电子性能随Ru负载的变化而变化。其中,1Ru/NA-Al2O3催化剂具有最佳尺寸的Ru物种(~ 0.8 nm)和定制的电子结构,通过有效抑制连续的C-C键裂解,显示出最高的PE氢解效率。该催化剂的PE转化率为1.15 × 103 g转化率为gRu−1 h−1,液/蜡产率为9.23 × 102 gliquid/wax gRu−1 h−1,在催化PE氢解方面表现出优异的性能。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Effective production of liquid/wax fuels from polyethylene plastics using Ru/Al2O3 catalysts†

Effective production of liquid/wax fuels from polyethylene plastics using Ru/Al2O3 catalysts†

Hydrogenolysis provides a promising pathway for converting polyolefin plastics into valuable liquid and wax fuels. This process involves dehydrogenation, C–C bond cleavage, and hydrogenation at the active metal sites of the catalyst. Controlling the nature of these metal sites is crucial to optimize overall reaction activity. In this study, Ru catalysts supported on nanosheet-assembled Al2O3 (NA-Al2O3) were used for the hydrogenolysis of polyethylene (PE). Unlike commercial Al2O3, NA-Al2O3 promotes Ru–Al bond formation, leading to stronger metal–support interactions. Under identical Ru loadings, these enhanced interactions resulted in higher Ru dispersion and smaller Ru species on the NA-Al2O3 surface. To investigate the effect of Ru loading, a series of catalysts (xRu/NA-Al2O3, x = 0.5, 1, 5, and 8 wt% Ru) was synthesized, revealing that Ru particle size and electronic properties varied with Ru loading. Among them, the 1Ru/NA-Al2O3 catalyst, featuring optimally sized Ru species (∼0.8 nm) and a tailored electronic structure, demonstrated the highest efficiency in PE hydrogenolysis by effectively suppressing successive C–C bond cleavage. This catalyst achieved an outstanding PE conversion rate of 1.15 × 103 gconverted PE gRu−1 h−1 and a liquid/wax production rate of 9.23 x 102 gliquid/wax gRu−1 h−1, highlighting its superior performance in catalytic PE hydrogenolysis.

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