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HKUST-1 Synthesis in PET Track-Etched Membranes via Conversion of Deposited Cu for Carbon Dioxide Capture

  • Dias D. Omertassov
  • , Aigerim Kh Shakayeva
  • , Zhanna K. Zhatkanbayeva
  • , Rafael I. Shakirzyanov
  • , Maxim V. Zdorovets
  • , Olgun Güven
  • , Ilya V. Korolkov
  • Institute of Nuclear Physics, National Nuclear Center of the Republic of Kazakhstan
  • L.N. Gumilyov Eurasian National University

Araştırma sonucu: Dergiye katkıMakalebilirkişi

7 Alıntılar (Scopus)

Özet

Climate change remains one of the most critical global challenges, largely driven by the rise in atmospheric CO2levels. Effective strategies for capturing and utilizing CO2are crucial to mitigate its environmental impact. Metal–organic frameworks (MOFs), particularly HKUST-1 (MOF-199), are promising materials due to their high surface area, porosity, and tunable properties. In this study, HKUST-1 was successfully immobilized on polyethylene terephthalate (PET) track-etched membranes, leveraging the membranes’ well-defined porosity and chemical stability. Membrane characterization via SEM revealed uniform coverage of octahedral HKUST-1 crystals with sizes ranging from 0.15 μm (inside the pores) to 1.5–5 μm (on the surface of the membrane). BET analysis of the PET TeMs-HKUST-1 composite membrane indicated a specific surface area of up to 382 m2/g. XRD confirmed the crystallinity of the HKUST-1 structure. The composite membranes exhibited CO2sorption capabilities, with an adsorption capacity of 0.53 ± 0.03 mmol/g (after 1 h of adsorption) in the first cycle for the solvothermal method and 0.31 ± 0.02 mmol/g (after 1 h of adsorption) for the solvoshaker method. Durability tests demonstrated a stable performance over 12 adsorption–desorption cycles. These results highlight the potential of PET TeMs-HKUST-1 composite membranes for scalable and efficient CO2capture, contributing to the development of sustainable solutions for addressing climate change.

Orijinal dilİngilizce
Sayfa (başlangıç-bitiş)30259-30271
Sayfa sayısı13
DergiACS Omega
Hacim10
Basın numarası28
DOI'lar
Yayın durumuYayınlandı - 22 Tem 2025

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