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A linker selective retention strategy to construct hierarchical porous metal-organic frameworks with high catalytic activity for oxidative desulfurization.
Sun, Xiaowen; Gu, Yun-Feng; Zhang, Xiao-Min; Shen, Yan; Wang, Dan-Hong; Zhang, Shu-Ming; Yu, Mei-Hui; Chang, Ze.
Afiliação
  • Sun X; School of Materials Science and Engineering, Nankai University, Tianjin 300350, China. mh@nankai.edu.cn.
  • Gu YF; School of Chemical Engineering and Technology, Hebei University of Technology, Tianjin 300130, China.
  • Zhang XM; College of Chemistry, Nankai University, Tianjin 300071, China.
  • Shen Y; School of Materials Science and Engineering, Nankai University, Tianjin 300350, China. mh@nankai.edu.cn.
  • Wang DH; School of Materials Science and Engineering, Nankai University, Tianjin 300350, China. mh@nankai.edu.cn.
  • Zhang SM; School of Chemical Engineering and Technology, Hebei University of Technology, Tianjin 300130, China.
  • Yu MH; School of Materials Science and Engineering, Nankai University, Tianjin 300350, China. mh@nankai.edu.cn.
  • Chang Z; School of Materials Science and Engineering, Nankai University, Tianjin 300350, China. mh@nankai.edu.cn.
Dalton Trans ; 53(14): 6157-6161, 2024 Apr 02.
Article em En | MEDLINE | ID: mdl-38488126
ABSTRACT
In order to improve the oxidative desulfurization (ODS) performance of MOF materials, an effective way is to convert a microporous MOF into a hierarchical porous MOF (HP-MOF) by utilizing the linker selective retention strategy. Herein, UiO-66 with the introduction of an unstable linker ligand (dihydro-1,2,4,5-tetrazine-3,6-dicarboxylate, dhtz) can selectively remove dhtz ligands to form HP-MOF (HP-UiO-66-dhtz) through heat treatment at high temperature. While maintaining the original structure of UiO-66, HP-UiO-66-dhtz features mesopores and abundant Lewis acid sites, showing excellent ODS performance for diphenylthiophene (DBT).

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2024 Tipo de documento: Article