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Amino-Functionalized Water-Stable Metal-Organic Framework for Enhanced C2H2/CH4 Separation Performance.
Li, Qian; Wu, Nana; Li, Jia; Wu, Dapeng; Li, Yanshuo.
Afiliação
  • Li Q; State Key Laboratory Base of Novel Functional Materials and Preparation Science, School of Materials Science & Chemical Engineering, Ningbo University, Ningbo, Zhejiang 315211, China.
  • Wu N; State Key Laboratory Base of Novel Functional Materials and Preparation Science, School of Materials Science & Chemical Engineering, Ningbo University, Ningbo, Zhejiang 315211, China.
  • Li J; State Key Laboratory Base of Novel Functional Materials and Preparation Science, School of Materials Science & Chemical Engineering, Ningbo University, Ningbo, Zhejiang 315211, China.
  • Wu D; State Key Laboratory Base of Novel Functional Materials and Preparation Science, School of Materials Science & Chemical Engineering, Ningbo University, Ningbo, Zhejiang 315211, China.
  • Li Y; State Key Laboratory Base of Novel Functional Materials and Preparation Science, School of Materials Science & Chemical Engineering, Ningbo University, Ningbo, Zhejiang 315211, China.
Inorg Chem ; 59(5): 2631-2635, 2020 Mar 02.
Article em En | MEDLINE | ID: mdl-32040303
ABSTRACT
Using a hydrothermal method, a water-stable metal-organic framework based on 8-connected Ni2 units with (4·62)2(47·613·83) topology, [Ni2(µ2-OH2)(ctpd)2(NH2-bdc)]·(EtOH)2·(H2O)2 (NbU-9-NH2), constructed by mixing a rigid tridentate ligand and an amino-p-carboxyl ligand, displays an enhanced ability for adsorbing C2H2 and adsorptive selectivity for C2H2/CH4. Dispersion-corrected density functional theory calculation confirmed that the enhenced acetylene adsorption is mainly derived from the weak hydrogen-bonding between a hydrogen atom of C2H2 and the nitrogen atom of the amino group.

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Ano de publicação: 2020 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Ano de publicação: 2020 Tipo de documento: Article