TY - JOUR
T1 - Thin-film composite mixed-matrix membrane with irregular micron-sized UTSA-16 for outstanding gas separation performance
AU - Min, Hyo Jun
AU - Kang, Miso
AU - Bae, Youn-Sang
AU - Blom, Richard
AU - Grande, Carlos A.
AU - Kim, Jong Hak
N1 - KAUST Repository Item: Exported on 2023-02-10
Acknowledgements: This work was supported by National Research Foundation of Korea (NRF) grants funded by the Korean government (MSIT) (2020K1A4A7A02095371, 2017R1D1A1B06028030), and by the Norwegian Research Council (NRC, grant number 267873).
PY - 2022/12/27
Y1 - 2022/12/27
N2 - Low-cost, micron-sized particles still pose a barrier to their use in thin-film composite mixed-matrix membranes (TFC-MMMs) owing to their poor interfacial contact with the polymer matrix. Also, the particles are too large to be fabricated into the submicron-thick membranes. Herein, we report high-performing, TFC-MMMs based on a CO2-philic comb copolymer, poly (tetrahydrofurfuryl methacrylate)–co–poly (poly (oxyethylene methacrylate)) (PTO), and an irregular, micron-sized, CO2-selective metal-organic framework (MOF), UTSA-16. The PTO comb copolymer matrix exhibited excellent film-forming ability, adhesion properties and showed a good gas separating performance. The PTO comb copolymer also enhanced the dispersibility of UTSA-16 in an environment-friendly solvent mixture (i.e., ethanol/water), which did not adversely damage the underlying porous polymeric support. Despite the micron-scale particle size of UTSA-16, PTO copolymer completely covered the surface of UTSA-16 via strong interactions without any deep pore infiltration and exhibited excellent interfacial contact properties. Consequently, defect-free TFC-MMMs with a polymer thickness of 300 nm were successfully prepared on the porous support. The TFC-MMM with 10% filler loading exhibited excellent CO2 permeance and selectivity, i.e., CO2 permeance of 1070 GPU, CO2/N2 selectivity of 41.0, CO2/CH4 selectivity of 17.2, outperforming the TFC-MMMs prepared with commercially available Pebax. All PTO-based MMMs, with the exception of the low content of UTSA-16 (5%), exceeded the gas separation performance required for post-combustion CO2 capture process.
AB - Low-cost, micron-sized particles still pose a barrier to their use in thin-film composite mixed-matrix membranes (TFC-MMMs) owing to their poor interfacial contact with the polymer matrix. Also, the particles are too large to be fabricated into the submicron-thick membranes. Herein, we report high-performing, TFC-MMMs based on a CO2-philic comb copolymer, poly (tetrahydrofurfuryl methacrylate)–co–poly (poly (oxyethylene methacrylate)) (PTO), and an irregular, micron-sized, CO2-selective metal-organic framework (MOF), UTSA-16. The PTO comb copolymer matrix exhibited excellent film-forming ability, adhesion properties and showed a good gas separating performance. The PTO comb copolymer also enhanced the dispersibility of UTSA-16 in an environment-friendly solvent mixture (i.e., ethanol/water), which did not adversely damage the underlying porous polymeric support. Despite the micron-scale particle size of UTSA-16, PTO copolymer completely covered the surface of UTSA-16 via strong interactions without any deep pore infiltration and exhibited excellent interfacial contact properties. Consequently, defect-free TFC-MMMs with a polymer thickness of 300 nm were successfully prepared on the porous support. The TFC-MMM with 10% filler loading exhibited excellent CO2 permeance and selectivity, i.e., CO2 permeance of 1070 GPU, CO2/N2 selectivity of 41.0, CO2/CH4 selectivity of 17.2, outperforming the TFC-MMMs prepared with commercially available Pebax. All PTO-based MMMs, with the exception of the low content of UTSA-16 (5%), exceeded the gas separation performance required for post-combustion CO2 capture process.
UR - http://hdl.handle.net/10754/687570
UR - https://linkinghub.elsevier.com/retrieve/pii/S0376738822010407
U2 - 10.1016/j.memsci.2022.121295
DO - 10.1016/j.memsci.2022.121295
M3 - Article
SN - 1873-3123
VL - 669
SP - 121295
JO - Journal of Membrane Science
JF - Journal of Membrane Science
ER -