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Design of a robust and strong-acid MOF platform for selective ammonium recovery and proton conductivity

Metal–organic frameworks (MOFs) are potential candidates for the platform of the solid acid; however, no MOF has been reported that has both aqueous ammonium stability and a strong acid site. This manuscript reports a highly stable MOF with a cation exchange site synthesized by the reaction between...

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Detalles Bibliográficos
Autores principales: Hatakeyama, Genki, Zhou, Hongyao, Kikuchi, Takashi, Nishio, Masaki, Oka, Kouki, Sadakiyo, Masaaki, Nishiyama, Yusuke, Yamada, Teppei
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society of Chemistry 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10466313/
https://www.ncbi.nlm.nih.gov/pubmed/37655037
http://dx.doi.org/10.1039/d3sc02743k
Descripción
Sumario:Metal–organic frameworks (MOFs) are potential candidates for the platform of the solid acid; however, no MOF has been reported that has both aqueous ammonium stability and a strong acid site. This manuscript reports a highly stable MOF with a cation exchange site synthesized by the reaction between zirconium and mellitic acid under a high concentration of ammonium cations (NH(4)(+)). Single-crystal XRD analysis of the MOF revealed the presence of four free carboxyl groups of the mellitic acid ligand, and the high first association constant (pK(a1)) of one of the carboxyl groups acts as a monovalent ion-exchanging site. NH(4)(+) in the MOF can be reversibly exchanged with proton (H(+)), sodium (Na(+)), and potassium (K(+)) cations in an aqueous solution. Moreover, the uniform nanospace of the MOF provides the acid site for selective NH(4)(+) recovery from the aqueous mixture of NH(4)(+) and Na(+), which could solve the global nitrogen cycle problem. The solid acid nature of the MOF also results in the proton conductivity reaching 1.34 × 10(−3) S cm(−1) at 55 °C by ion exchange from NH(4)(+) to H(+).