TY - JOUR
T1 - Mixed-Linker Metal-Organic frameworks for carbon and hydrocarbons capture under moist conditions
AU - Gu, Yi Ming
AU - Yuan, You You
AU - Qadir, Salman
AU - Yuan, Zhong Shan
AU - Zhao, Sheng Sheng
AU - Sun, Tian Jun
AU - Liu, Xiao Wei
AU - Wang, Shu Dong
N1 - KAUST Repository Item: Exported on 2022-01-19
Acknowledgements: The authors thank the National Natural Science Foundation of China for support under the grant of No. 21776266. The authors are also grateful to Yangquan Coal Industry (Group) Co. LTD. China for support of the R&D project “Upgrade of 300 Nm3/h Low-Concentration Coal Bed methane by a Rapid Cycle Pressure Swing Adsorption Process”. The authors acknowledge Dr. Chang Wang and Dr. Pei-Fang Yan for the at Division of Energy Research Resources, DICP, for their support in structure measurement; Dr. Jiang-Wei Zhang and Dr. Jing-Xu Li for the help in XRD refinement and advanced mass spectrometer technology.
PY - 2022/1/4
Y1 - 2022/1/4
N2 - The capture of carbon and hydrocarbons is significant to the utilization of valuable resources and the mitigation of global warming, but achieving high gas capacity and selectivity at the same time remains a challenge, especially in the presence of high humidity. In this regard, based on the building block of MOF-801, MOF-801-FA structures were synthesized with high quality and few defects through a mixed-ligand strategy, in which formate ligands were introduced into the framework apart from fumarate ligands. This brought about tremendous increases in gas adsorption capacity, e.g., ca. 2.5-fold and 1.1-fold enhancement occurred to the adsorption of CH4 and CO2 in MOF-801-Hf-FA than MOF-801-Hf at 298 K and 1 bar. Besides, prominent IAST selectivities were also witnessed in MOF-801-FA, higher than those in the pristine MOFs, for CH4/N2 and CO2/N2 mixtures under ambient conditions. We then confirmed the efficient performance of MOF-801-FA for real CH4/N2 and CO2/N2 mixtures using the breakthrough experiments and following cycling tests, even in a relative humidity of 90%. Thus, the mixed-linker strategy was demonstrated effective to tune the structures of MOFs, and boost their performance in gas adsorption and separation. The results also showed that, with high capacities for CH4 and CO2, superior selectivities over N2, desirable water resistance and facile regeneration, MOF-801-M−FA (M = Zr or Hf) are promising candidates for capturing CH4 and CO2 from N2 in industry.
AB - The capture of carbon and hydrocarbons is significant to the utilization of valuable resources and the mitigation of global warming, but achieving high gas capacity and selectivity at the same time remains a challenge, especially in the presence of high humidity. In this regard, based on the building block of MOF-801, MOF-801-FA structures were synthesized with high quality and few defects through a mixed-ligand strategy, in which formate ligands were introduced into the framework apart from fumarate ligands. This brought about tremendous increases in gas adsorption capacity, e.g., ca. 2.5-fold and 1.1-fold enhancement occurred to the adsorption of CH4 and CO2 in MOF-801-Hf-FA than MOF-801-Hf at 298 K and 1 bar. Besides, prominent IAST selectivities were also witnessed in MOF-801-FA, higher than those in the pristine MOFs, for CH4/N2 and CO2/N2 mixtures under ambient conditions. We then confirmed the efficient performance of MOF-801-FA for real CH4/N2 and CO2/N2 mixtures using the breakthrough experiments and following cycling tests, even in a relative humidity of 90%. Thus, the mixed-linker strategy was demonstrated effective to tune the structures of MOFs, and boost their performance in gas adsorption and separation. The results also showed that, with high capacities for CH4 and CO2, superior selectivities over N2, desirable water resistance and facile regeneration, MOF-801-M−FA (M = Zr or Hf) are promising candidates for capturing CH4 and CO2 from N2 in industry.
UR - http://hdl.handle.net/10754/674953
UR - https://linkinghub.elsevier.com/retrieve/pii/S1385894721060174
UR - http://www.scopus.com/inward/record.url?scp=85122499809&partnerID=8YFLogxK
U2 - 10.1016/j.cej.2021.134447
DO - 10.1016/j.cej.2021.134447
M3 - Article
SN - 1385-8947
VL - 433
SP - 134447
JO - Chemical Engineering Journal
JF - Chemical Engineering Journal
ER -