Porous graphene nanosheets functionalized thin film nanocomposite membrane prepared by interfacial polymerization for CO2/N2 separation

被引:41
|
作者
Li, Hui [1 ,2 ]
Ding, Xiaoxu [1 ]
Zhang, Yatao [1 ,2 ]
Liu, Jindun [1 ,2 ]
机构
[1] Zhengzhou Univ, Sch Chem Engn & Energy, Zhengzhou 450001, Henan, Peoples R China
[2] Zhengzhou Key Lab Adv Separat Technol, Zhengzhou 450001, Henan, Peoples R China
基金
中国国家自然科学基金;
关键词
Porous graphene; Interfacial polymerization; Thin film nanocomposite (TFN) membranes; CO2; capture; MIXED-MATRIX MEMBRANES; WALLED CARBON NANOTUBES; GAS SEPARATION; CO2; SEPARATION; INORGANIC FILLERS; HYBRID MEMBRANES; OXIDE MEMBRANES; HOLLOW-FIBER; PERFORMANCE; TRANSPORT;
D O I
10.1016/j.memsci.2017.08.046
中图分类号
TQ [化学工业];
学科分类号
0817 ;
摘要
The inherent defects of porous graphene (PG) formed during reduction etching process could serve as nanopores, making PG emerge a potential application for the preparation of micrometre-sized separation membranes. Here, we introduced PG as inorganic nanofiller to fabricate thin film nanocomposite (TFN) membranes for CO2 capture via interfacial polymerization technique. The PG selective nanolayers not only possessed a good adhesion with polymers but also benefited from hydrogen bonding actions, simultaneously, thus ensuring the formation of high-efficiency molecular sieving passageway in the separation layer of membranes. Furthermore, the thin PG nanosheets were verified to have an significantly affect for permeability and selectivity of membranes (PG, 0.05 wt%, 1 bar), with exhibiting about 21% and 20.8% enhancement of the CO2 permeance and the CO2/N-2 selectively compared to that of the membrane without PG separately. Simultaneously, the membrane also showed higher stability and the porous surface morphology of PG shortened greatly the gas transfer path. The approach offers a potential promising to exploit the ultra-thin film composite membrane for efficient gas separation.
引用
收藏
页码:58 / 68
页数:11
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