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Title: The effects of chemical structure on gas transport properties of poly(aryl ether ketone) random copolymers
Authors: Chng, M.L. 
Xiao, Y. 
Chung, T.S. 
Toriida, M.
Tamai, S.
Keywords: Gas permeation
Poly(aryl ether ketone)
Random copolymer
Issue Date: 5-Jan-2007
Citation: Chng, M.L., Xiao, Y., Chung, T.S., Toriida, M., Tamai, S. (2007-01-05). The effects of chemical structure on gas transport properties of poly(aryl ether ketone) random copolymers. Polymer 48 (1) : 311-317. ScholarBank@NUS Repository.
Abstract: The physical properties and gas permeation behavior of a series of homo/random copolymers of 4,4′-difluorobenzophenone (DFBP)-2,2-bis(4-hydroxy-phenyl)propane (BPA)/2,2-bis(4-hydroxy-3,5-dimethyl-phenyl)propane (TMBPA) have been investigated by systematically varying the diol ratios. The tetramethyl substitution group on the phenyl rings simultaneously increases polymer free volume and chain stiffness. These were confirmed by experimental and simulated methods. With the increase in TMBPA content, the gas permeation coefficients, diffusion and solubility coefficients of H2, O2, N2, CO2 and CH4 were found to increase. The gas transport coefficients of the copolymers predicted from the additional rule were compared with the experimental results and the results obtained were within the expectations. In addition, the logarithm of gas permeation coefficients and the reciprocal of fractional free volume (1/FFV) also exhibited a good correlation. However, with the incorporation of TMBPA moiety, the permselectivity of gas pairs such as H2/N2, O2/N2 and CO2/CH4 remains reasonably high. As a result, the gas separation performance of TMBPA modified poly(aryl ether ketone) approaches the upper bound of the corresponding gas pairs. After comparing this work with gas separation performance of other methyl substituted polymers, one may conclude there is a general phenomenon that methyl substitution increases the gas permeability of the modified polymer with a small loss in gas selectivity for small gas pairs. © 2006 Elsevier Ltd. All rights reserved.
Source Title: Polymer
ISSN: 00323861
DOI: 10.1016/j.polymer.2006.11.009
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