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Sorption-Enhanced Mixed Matrix Membranes with Facilitated Hydrogen Transport for Hydrogen Purification and CO2 Capture
被引:56
作者:
Zhu, Lingxiang
[1
]
Yin, Deqiang
[1
]
Qin, Yueling
[2
]
Konda, Shailesh
[1
]
Zhang, Shawn
[3
]
Zhu, Aiden
[3
]
Liu, Shuai
[4
,5
]
Xu, Ting
[4
,5
,6
]
Swihart, Mark T.
[1
]
Lin, Haiqing
[1
]
机构:
[1] SUNY Buffalo, Dept Chem & Biol Engn, Buffalo, NY 14260 USA
[2] SUNY Buffalo, Dept Phys, Buffalo, NY 14260 USA
[3] DigiM Solut LLC, Burlington, MA 01803 USA
[4] Univ Calif Berkeley, Dept Chem, Berkeley, CA 94720 USA
[5] Lawrence Berkeley Natl Lab, Div Mat Sci, Berkeley, CA 94720 USA
[6] Univ Calif Berkeley, Dept Mat Sci & Engn, Berkeley, CA 94720 USA
基金:
美国国家科学基金会;
关键词:
CO2;
capture;
H-2;
separation;
mixed matrix membranes;
nanocomposites;
solubility;
ORGANIC FRAMEWORK NANOSHEETS;
CARBON CAPTURE;
SEPARATION;
PERFORMANCE;
POLYMERS;
GRAPHENE;
STORAGE;
D O I:
10.1002/adfm.201904357
中图分类号:
O6 [化学];
学科分类号:
0703 ;
摘要:
Mixed matrix membranes (MMMs) comprising size-sieving fillers dispersed in polymers exhibit diffusivity selectivity and may surpass the upper bound for gas separation, but their performance is limited by defects at the polymer/filler interface. Herein, a fundamentally different approach employing a highly sorptive filler that is inherently less sensitive to interfacial defects is reported. Palladium nanoparticles with extremely high H-2 sorption are dispersed in polybenzimidazole at loadings near the percolation threshold, which increases both H-2 permeability and H-2/CO2 selectivity. Performance of these MMMs surpasses the state-of-the-art upper bound for H-2/CO2 separation with polymer-based membranes. The success of these sorption-enhanced MMMs for H-2/CO2 separation may launch a new research paradigm that taps the enormous knowledge of affinities between gases and nanomaterials to design MMMs for a wide variety of gas separations.
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