z-logo
Premium
A novel composite derived from a metal organic framework immobilized within electrospun nanofibrous polymers: An efficient methane adsorbent
Author(s) -
Sargazi Ghasem,
Afzali Daryoush,
Mostafavi Ali,
Kazemian Hossein
Publication year - 2020
Publication title -
applied organometallic chemistry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.53
H-Index - 71
eISSN - 1099-0739
pISSN - 0268-2605
DOI - 10.1002/aoc.5448
Subject(s) - adsorption , polyvinyl alcohol , chemical engineering , composite number , chemistry , nanofiber , electrospinning , porosity , polymer , crystallinity , methane , metal organic framework , response surface methodology , thermal stability , materials science , composite material , organic chemistry , chromatography , engineering
In this study, tantalum(V) metal organic framework (Ta‐MOF) nanostructure was incorporated within polyvinyl alcohol (PVA) nanofibers to prepare an electrospun porous composite as a novel CH 4 adsorbent. The crystallinity, thermodynamic behavior, and textural properties of the products were investigated using instrumental analyses techniques. The results confirmed that the developed PVA/Ta‐MOF electrospun nanofibrous composite exhibits higher thermal stability, considerable porosity, and larger surface area compared to the parent Ta‐MOF. A 2 k factorial design was used for systematic study of the adsorption process. The results of response surface methodology (RSM) optimization indicated that the highest methane adsorption can be achieved at 24.40 °C and 3.70 bar in 23.60 min. These nano pore sorbents showed a significant potential for CH 4 adsorption due to the presence of Ta‐MOF at the surface of nanofibrous composite compared to many other conventional sorbents that have been already used. This study introduces a novel biocompatible/biodegradable nanofibrous composite material with high methane adsorption performance and potentials for other applications.

This content is not available in your region!

Continue researching here.

Having issues? You can contact us here