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.
引用
收藏
页数:7
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