TY - JOUR
T1 - Moisture-tolerant diamine-appended metal–organic framework composites for effective indoor CO2 capture through facile spray coating
AU - Seok Chae, Yun
AU - Park, Sookyung
AU - Won Kang, Dong
AU - Won Kim, Dae
AU - Kang, Minjung
AU - San Choi, Doo
AU - Hyeak Choe, Jong
AU - Seop Hong, Chang
N1 - Funding Information:
This work was supported by the Basic Science Research Program (NRF-2021R1A2B5B03086313) and the Priority Research Centers Program (NRF-2019R1A6A1A11044070). We thank the Institute for Basic Science (IBS) Center for Molecular Spectroscopy and Dynamics (IBS-R023-D1) for providing NMR spectrometry and professional technical support.
Publisher Copyright:
© 2021 Elsevier B.V.
PY - 2022/4/1
Y1 - 2022/4/1
N2 - Reducing the concentration of indoor carbon dioxide (CO2) to an acceptable safe level of 1,000 ppm is an important issue because a high level of CO2 in closed spaces causes lethargy and fatigue. Although diamine-functionalized metal–organic framework (MOF) adsorbents with high CO2 capacities under indoor air conditions are available, the moisture-induced degradation of MOFs and their shaping remains a challenge for practical applications. Herein, we report the fabrication of epn-functionalized Mg2(dobpdc) composites, which proceeded by mixing with a polystyrene-block-polybutadiene-block-polystyrene (SBS) hydrophobic polymer (epn = 1-ethylpropane-1,3-diamine; dobpdc4− = 4,4′-dioxido-3,3′-biphenyldicarboxylate). The composites were successfully shaped in the form of membranes with different amounts of MOF (epn-MOFX@SBS; X = 60–80 wt%). Specifically, epn-MOF80@SBS exhibited a significant CO2 adsorption of 2.8 mmol g−1 at 1,000 ppm with recyclable working capacity. The composites were further coated on the surfaces of different supports, such as a Ti mesh, an air filter, and granular activated carbon via a facile and simple spraying method. The experimental conditions were 1,000 ppm CO2 and 60% relative humidity in a 50-L chamber; the coated materials displayed invariant CO2 removal performances over 10 cycles and even after 7 days of exposure. The recyclable and long-term CO2 adsorption capacities demonstrate that the MOF-polymer composites and their coating on various supports provide a useful and effective route for indoor CO2 capture under realistic conditions.
AB - Reducing the concentration of indoor carbon dioxide (CO2) to an acceptable safe level of 1,000 ppm is an important issue because a high level of CO2 in closed spaces causes lethargy and fatigue. Although diamine-functionalized metal–organic framework (MOF) adsorbents with high CO2 capacities under indoor air conditions are available, the moisture-induced degradation of MOFs and their shaping remains a challenge for practical applications. Herein, we report the fabrication of epn-functionalized Mg2(dobpdc) composites, which proceeded by mixing with a polystyrene-block-polybutadiene-block-polystyrene (SBS) hydrophobic polymer (epn = 1-ethylpropane-1,3-diamine; dobpdc4− = 4,4′-dioxido-3,3′-biphenyldicarboxylate). The composites were successfully shaped in the form of membranes with different amounts of MOF (epn-MOFX@SBS; X = 60–80 wt%). Specifically, epn-MOF80@SBS exhibited a significant CO2 adsorption of 2.8 mmol g−1 at 1,000 ppm with recyclable working capacity. The composites were further coated on the surfaces of different supports, such as a Ti mesh, an air filter, and granular activated carbon via a facile and simple spraying method. The experimental conditions were 1,000 ppm CO2 and 60% relative humidity in a 50-L chamber; the coated materials displayed invariant CO2 removal performances over 10 cycles and even after 7 days of exposure. The recyclable and long-term CO2 adsorption capacities demonstrate that the MOF-polymer composites and their coating on various supports provide a useful and effective route for indoor CO2 capture under realistic conditions.
KW - Hydrophobicity
KW - Indoor carbon dioxide capture
KW - MOF coating
KW - Metal-organic framework composites
UR - http://www.scopus.com/inward/record.url?scp=85123890738&partnerID=8YFLogxK
U2 - 10.1016/j.cej.2021.133856
DO - 10.1016/j.cej.2021.133856
M3 - Article
AN - SCOPUS:85123890738
SN - 1385-8947
VL - 433
JO - Chemical Engineering Journal
JF - Chemical Engineering Journal
M1 - 133856
ER -