Effect of Raw Multi-Wall Carbon Nanotubes on Morphology and Separation Properties of Polyimide Membranes

被引:32
|
作者
Aroon, M. A. [1 ,2 ]
Ismail, A. F. [2 ]
Montazer-Rahmati, M. M. [1 ]
Matsuura, T. [2 ,3 ]
机构
[1] Univ Tehran, Coll Engn, Sch Chem Engn, Membrane Res Lab, Tehran, Iran
[2] Univ Teknol Malaysia, Adv Membrane Technol Ctr AMTEC, Skudai, Johor Bahru, Malaysia
[3] Univ Ottawa, Dept Chem & Biol Engn, Ind Membrane Res Lab, Ottawa, ON, Canada
关键词
gas separation; mixed matrix membranes; multi wall carbon nanotubes; MIXED-MATRIX MEMBRANES; COMPRISING ORGANIC POLYMERS; GAS SEPARATION; MECHANICAL-PROPERTIES; MOLECULAR-SIEVES; PERMEABILITY; PURIFICATION; POLYSULFONE; PERFORMANCE; NANOCOMPOSITES;
D O I
10.1080/01496395.2010.484007
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Raw multi wall carbon nanotubes (r-MWCNTs) were embedded as fillers inside the polyimide (PI) matrix and PI/r-MWCNTs mixed matrix membranes were fabricated by the phase inversion method. The TEM images and permeation results using helium as test gas showed that r-MWCNTs were generally closed ended and acted as impermeable nano particles. Gas permeation tests using CO2 and CH4 showed that the addition of r-MWCNTs into the dope solution increased the CO2/CH4 separation factor while decreasing the carbon dioxide and methane permeances. When the r-MWCNTs content was increased from 0% to 6wt.%, permeance of CO2 in the flat sheet mixed matrix membranes decreased from 9.15 GPU to 5.49 GPU and CO2/CH4 separation factor increased from 19.05 to 45.75. Identical to flat sheet mixed matrix membranes, the addition of 2wt.% r-MWCNTs into a spinning dope increased the CO2/CH4 separation factor from 46.61 to 72.20. The glass transition temperature of the mixed matrix flat sheet membranes increased with an increase in the r-MWCNTs content. This implies a good segmental-level attachment between the two phases that forms a rigidified polymer region at the polymer/r-MWCNTs interface. FESEM images showed well dispersed r-MWCNTs in the polymer matrix at a loading of 2wt% r-MWCNTs.
引用
收藏
页码:2287 / 2297
页数:11
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