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Polystyrene Waste Thermochemical Hydrogenation to Ethylbenzene by a N-Bridged Co, Ni Dual-Atom Catalyst.
Li, Runze; Zhang, Zedong; Liang, Xiao; Shen, Ji; Wang, Jia; Sun, Wenming; Wang, Dingsheng; Jiang, Jianchun; Li, Yadong.
Afiliação
  • Li R; Department of Chemistry, Tsinghua University, Beijing 100084, China.
  • Zhang Z; Department of Chemistry, Tsinghua University, Beijing 100084, China.
  • Liang X; Department of Chemistry, Tsinghua University, Beijing 100084, China.
  • Shen J; Department of Chemistry, Tsinghua University, Beijing 100084, China.
  • Wang J; Jiangsu Co-Innovation Center for Efficient Processing and Utilization of Forest Resources, College of Chemical Engineering, Nanjing Forestry University, Longpan Road 159, Nanjing 210037, China.
  • Sun W; Institute of Chemical Industry of Forest Products, Chinese Academy of Forestry, Nanjing 210042, China.
  • Wang D; Department of Chemistry, Beijing Key Laboratory for Optical Materials and Photonic Devices, Capital Normal University, Beijing 100048, China.
  • Jiang J; Department of Chemistry, Tsinghua University, Beijing 100084, China.
  • Li Y; Jiangsu Co-Innovation Center for Efficient Processing and Utilization of Forest Resources, College of Chemical Engineering, Nanjing Forestry University, Longpan Road 159, Nanjing 210037, China.
J Am Chem Soc ; 145(29): 16218-16227, 2023 Jul 26.
Article em En | MEDLINE | ID: mdl-37438261
ABSTRACT
Recycling waste plastics requires the degradation of plastics into small molecules. However, various products are widely distributed using traditional methods of depolymerizing polystyrene (PS) such as catalytic pyrolysis and hydrogenolysis. Here, we creatively report a N-bridged Co, Ni dual-atom (Co-N-Ni) catalyst for the targeted conversion of waste PS plastics to ethylbenzene via a pressurized tandem fixed-bed reactor where hydropyrolysis is coupled with downstream vapor-phase hydrotreatment. The Co-N-Ni catalyst achieves 95 wt % PS conversion with 92 wt % ethylbenzene yield, significantly superior to the corresponding single-atom catalysts, and enables degradation of real PS plastics. Theoretical calculations and experimental results demonstrate that the d-band center of metal atoms is well regulated in the Co-N-Ni catalyst. The Co site activates the C═C bond more easily, while the Ni site spatially optimizes the adsorption configuration of the styrene molecule due to the electronic interaction. This Co-N-Ni catalyst in the tandem reactor also shows excellent durability and provides a new direction for real plastic degradation.

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: J Am Chem Soc Ano de publicação: 2023 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: J Am Chem Soc Ano de publicação: 2023 Tipo de documento: Article