Reduced graphene oxide aerogel membranes fabricated through hydrogen bond mediation for highly efficient oil/water separation

被引:55
作者
He, Mingrui [1 ,2 ]
Zhang, Runnan [1 ,2 ]
Zhang, Kan [1 ,2 ]
Liu, Yanan [1 ,2 ]
Su, Yanlei [1 ,2 ]
Jiang, Zhongyi [1 ,2 ]
机构
[1] Tianjin Univ, Sch Chem Engn & Technol, Key Lab Green Chem Technol, Tianjin 300072, Peoples R China
[2] Collaborat Innovat Ctr Chem Sci & Engn Tianjin, Tianjin 300072, Peoples R China
基金
中国国家自然科学基金;
关键词
IN-SITU; PORE-SIZE; REDUCTION; COMPOSITE;
D O I
10.1039/c9ta01700c
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Reduced graphene oxide aerogels (rGOAs) are broadly applied in energy and environmentally relevant fields. However, rGOAs have been rarely reported for fabrication of separation membranes. In this study, we demonstrate the fabrication of reduced graphene oxide aerogel membranes (rGOAMs) via reduction-induced self-assembly of rGO through hydrogen bond mediation. When using polyethylene glycol (PEG) as the mediator, the PEG-rGO hydrogen bonding interactions partly replace interlayer - and hydrophobic interactions during reduction, decreasing the rGO laminates' size in 2D stacking and alleviating the structural shrinkage of rGOA networks. The tight correlation between membrane pore size and porosity was broken, leading to rGOAMs with tunable pore sizes (0.62 to 0.33 m) and high porosity (approximate to 95%). The resultant rGOAMs can effectively reject oil-in-water emulsions with different sizes and exhibit ultrahigh water fluxes (up to 4890 L m(-2) h(-1)) under 0.10 bar as well as a persistent anti-oil-fouling performance up to 6 cycles. Three other kinds of hydrophilic polymers including polyvinyl alcohol, polyglycine and polyvinyl pyrrolidone are also utilized as mediators to elucidate the structure-performance relationship. Molecular simulation reveals that the pore size of rGOAMs is strongly affected by the hydrogen bond interaction intensity of the rGO-polymer and polymer size.
引用
收藏
页码:11468 / 11477
页数:10
相关论文
共 49 条
[1]   Density Functional Theory and Hydrogen Bonds: Are We There Yet? [J].
Boese, A. Daniel .
CHEMPHYSCHEM, 2015, 16 (05) :978-985
[2]   Dynamic Ordering and Phase Segregation in Hydrogen-Bonded Polymers [J].
Chen, Senbin ;
Binder, Wolfgang H. .
ACCOUNTS OF CHEMICAL RESEARCH, 2016, 49 (07) :1409-1420
[3]   In situ self-assembly of mild chemical reduction graphene for three-dimensional architectures [J].
Chen, Wufeng ;
Yan, Lifeng .
NANOSCALE, 2011, 3 (08) :3132-3137
[4]   Self-Assembled Polyvinyl Alcohol Tannic Acid Hydrogels with Diverse Microstructures and Good Mechanical Properties [J].
Chen, Ya-Nan ;
Jiao, Chen ;
Zhao, Yaxin ;
Zhang, Jianan ;
Wang, Huiliang .
ACS OMEGA, 2018, 3 (09) :11788-11795
[5]   Tuning the Mechanical Properties of Graphene Oxide Paper and Its Associated Polymer Nanocomposites by Controlling Cooperative Intersheet Hydrogen Bonding [J].
Compton, Owen C. ;
Cranford, Steven W. ;
Putz, Karl W. ;
An, Zhi ;
Brinson, L. Catherine ;
Buehler, Markus J. ;
Nguyen, SonBinh T. .
ACS NANO, 2012, 6 (03) :2008-2019
[6]   Evaluations of the accuracies of DMol3 density functionals for calculations of experimental binding enthalpies of N2, CO, H2, C2H2 at catalytic metal sites [J].
Dance, Ian .
MOLECULAR SIMULATION, 2018, 44 (07) :568-581
[7]  
Dassault Systemes BIOVIA, 2014, MAT STUD 8 0
[8]   FEMTOSECOND MOLECULAR-DYNAMICS OF TAUTOMERIZATION IN MODEL BASE-PAIRS [J].
DOUHAL, A ;
KIM, SK ;
ZEWAIL, AH .
NATURE, 1995, 378 (6554) :260-263
[9]   Polymeric nanofiltration of binary water-alcohol mixtures: Influence of feed composition and membrane properties on permeability and rejection [J].
Geens, J ;
Peeters, K ;
Van der Bruggen, B ;
Vandecasteele, C .
JOURNAL OF MEMBRANE SCIENCE, 2005, 255 (1-2) :255-264
[10]   Effect of pore size on the interfacial resistance of a porous membrane [J].
Glavatskiy, K. S. ;
Bhatia, Suresh K. .
JOURNAL OF MEMBRANE SCIENCE, 2017, 524 :738-745