Application of surface modifying macromolecules in polyethersulfone membranes: Influence on PES surface chemistry and physical properties

被引:0
|
作者
Pham, VA
Santerre, JP
Matsuura, T
Narbaitz, RM
机构
[1] Univ Toronto, Fac Dent, Dept Biomat, Toronto, ON M5G 1G6, Canada
[2] Univ Ottawa, Dept Chem Engn, Ind Membrane Res Inst, Ottawa, ON K1N 6N5, Canada
[3] Univ Ottawa, Dept Civil Engn, Ottawa, ON K1N 6N5, Canada
关键词
membrane; pervaporation; polyethersulfone; surface active additive; fluorinated macromolecules;
D O I
暂无
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
Novel surface modifying macromolecules (SMMs) were developed for incorporation into polyethersulfone (PES) membranes, intended for pervaporation applications. These materials were synthesized with a diisocyanate, polypropylene oxide (PPO), and a fluoro-alcohol, and characterized for elemental analysis, molecular weight, and glass transition temperatures. PES/SMM blends with eight types of SMMs were characterized for surface and physical properties and compared with PES. Water droplet contact angle measurements and X-ray photoelectron spectroscopy data showed that the SMMs migrated to the surface and rendered the PES material more hydrophobic. While advancing contact angle data were equivalent to those of pure Teflon(TM) the highest average values of receding angles of these systems were less than those commercial Teflon(TM). The opaqueness of PES/SMMs films and data from differential scanning calorimetry experiments showed that the SMMs were either immiscible or only partially miscible with PES. It was also observed, for a fixed PES concentration of 25 wt %, that increases in the molecular weight of the SMMs and the weight fraction of PPO in the SMMs led to phase separation in the ternary PES/SMMs/dimethylacetamide (i.e., membrane casting solution) system. On the other hand, in the binary PES/SMMs system (i.e., cast membrane film), an increasing weight fraction of fluorine in the SMMs contributed to an increase in the phase separation. (C) 1999 John Wiley & Sons, Inc.
引用
收藏
页码:1363 / 1378
页数:16
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