AI Article Synopsis

  • Precious metals like palladium and platinum are diminishing, making recovery methods essential, especially in harsh conditions.
  • Zr(IV)-based metal-organic frameworks (MOFs) are effective for recovery, but their powder form limits real-world use, leading to the development of porous MOF-based membranes that offer high metal ion permeability and stability.
  • The study presents polymeric fibrous membranes with UiO-66, demonstrating excellent adsorption and desorption of Pd and Pt in acidic solutions, showcasing their compatibility, strong acid resistance, and significant performance in various systems.

Article Abstract

Precious metals such as palladium (Pd) and platinum (Pt) are marvelous materials in the fields of electronic and catalysis, but they are tapering day by day. Zr(IV)-based metal-organic frameworks (MOFs) are competent for their recovery, notably in harsh environments, while the general powder form limits their practical application. Porous MOF-based membranes with ultraefficient metal ion permeation, strong stability, and high selectivity are, therefore, strikingly preferred. Herein, a set of polymeric fibrous membranes incorporated with the UiO-66 series are fabricated; their adsorption/desorption capabilities toward Pd(II) and Pt(IV) are evaluated from strongly acidic solutions; and the MOF-polymer compatibilities are investigated. Polyurethane (PU)/UiO-66-NH showed strong acid resistance and high chemical stability, which are attributable to strong π-π interactions between PU and MOF nanoparticles with a high configuration of energy. The as-fabricated MOF membranes show extremely good adsorption/desorption performances without ruptures/coalitions of nanofibers or leak of MOF nanoparticles, and successfully display the efficacy in a gravity-driven or even continuous-flow system with good recycle performance and selectivity. The as-fabricated MOF membranes set an example of potential MOF-polymer compatibility for practical applications.

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Source
http://dx.doi.org/10.1002/smll.201805242DOI Listing

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