Zichittella Guido, Ebrahim Amani M, Zhu Jie, Brenner Anna E, Drake Griffin, Beckham Gregg T, Bare Simon R, Rorrer Julie E, Román-Leshkov Yuriy
Department of Chemical Engineering, Massachusetts Institute of Technology, Cambridge, Massachusetts 02139, United States.
SLAC National Accelerator Laboratory, Menlo Park, California 94025, United States.
JACS Au. 2022 Oct 5;2(10):2259-2268. doi: 10.1021/jacsau.2c00402. eCollection 2022 Oct 24.
The development of technologies to recycle polyethylene (PE) and polypropylene (PP), globally the two most produced polymers, is critical to increase plastic circularity. Here, we show that 5 wt % cobalt supported on ZSM-5 zeolite catalyzes the solvent-free hydrogenolysis of PE and PP into propane with weight-based selectivity in the gas phase over 80 wt % after 20 h at 523 K and 40 bar H. This catalyst significantly reduces the formation of undesired CH (≤5 wt %), a product which is favored when using bulk cobalt oxide or cobalt nanoparticles supported on other carriers (selectivity ≤95 wt %). The superior performance of Co/ZSM-5 is attributed to the stabilization of dispersed oxidic cobalt nanoparticles by the zeolite support, preventing further reduction to metallic species that appear to catalyze CH generation. While ZSM-5 is also active for propane formation at 523 K, the presence of Co promotes stability and selectivity. After optimizing the metal loading, it was demonstrated that 10 wt % Co/ZSM-5 can selectively catalyze the hydrogenolysis of low-density PE (LDPE), mixtures of LDPE and PP, as well as postconsumer PE, showcasing the effectiveness of this technology to upcycle realistic plastic waste. Cobalt supported on zeolites FAU, MOR, and BEA were also effective catalysts for C-C hydrocarbon formation and revealed that the framework topology provides a handle to tune gas-phase selectivity.
开发回收全球产量最高的两种聚合物——聚乙烯(PE)和聚丙烯(PP)的技术,对于提高塑料循环利用率至关重要。在此,我们表明,负载在ZSM-5沸石上的5 wt%钴在523 K和40 bar氢气条件下,20小时后能在气相中以超过80 wt%的重量选择性将PE和PP无溶剂氢解为丙烷。该催化剂显著减少了不期望的CH(≤5 wt%)的生成,而使用负载在其他载体上的块状氧化钴或钴纳米颗粒时,CH是更易生成的产物(选择性≤95 wt%)。Co/ZSM-5的优异性能归因于沸石载体对分散的氧化钴纳米颗粒的稳定作用,防止其进一步还原为似乎催化CH生成的金属物种。虽然ZSM-5在523 K时也对丙烷形成有活性,但钴的存在促进了稳定性和选择性。在优化金属负载量后,证明10 wt%的Co/ZSM-5可以选择性催化低密度聚乙烯(LDPE)、LDPE与PP的混合物以及消费后PE的氢解,展示了该技术升级回收实际塑料废弃物的有效性。负载在FAU、MOR和BEA沸石上的钴也是用于C-C烃形成的有效催化剂,并表明骨架拓扑结构为调节气相选择性提供了手段。