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NAMS 2002 Workshop - ICOM 2008

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introduction of methyl groups into the main chain polyamide component was<br />

carried out, in which a new macromonomer, 3,5-bis(4-amino-3-<br />

methylphenoxy)benzyloxypropyl- terminated polydimethylsiloxane (BAMPB-<br />

PDMS) was synthesized instead of BAPB- PDMS. Generally, it has been known<br />

that the introduction of alkyl group into aromatic polyamides could achieve the<br />

improvement of their solubility. The polycondensation of BAMPB-PDMS with<br />

terephthaloyl chloride yielded the desired siloxane-grafted polyamide<br />

copolymers, MPA-g-PDMS. The copolymer membranes were prepared by<br />

solvent casting method, and the gas permeability and pervaporation property of<br />

these membranes were evaluated. PA-g-PDMS was insoluble in any solvents<br />

after the copolymer was dried in vacuo, however, MPA-g-PDMS was soluble in<br />

solvents, such as tetrahydrofuran, chloroform and dichloromethane, even after it<br />

was completely dried. Therefore, MPA-g- PDMS exhibited the higher<br />

processability than PA-g-PDMS. Then, the measurement of stress-strain<br />

behavior of copolymer membranes was carried out, and these copolymer<br />

membranes showed the high mechanical strength. The gas permeability property<br />

of PA-g-PDMS and MPA-g-PDMS membranes was as same as that of the PDMS<br />

cross-linking membrane for all of the gases. In addition, gas permeability of these<br />

membranes were increased as increase of PDMS segment length, and these<br />

values of MPA-g-PDMS were slightly higher than those of PA- g-PDMS<br />

containing the same PDMS segment length. From the results of pervaporation of<br />

the dilute aqueous solutions of organic solvents, it was found that both of PA-g-<br />

PDMS and MPA-g- PDMS exhibited the excellent permselectivity toward several<br />

organic solvents, such as alcohols, acetone, tetrahydrofuran, chloroform,<br />

dichloromethane and benzene with a high and stable permeation. Such a high<br />

selectivity for organic liquids would be due to the hydrophobic surface covered<br />

with PDMS segments and the high permeability of the PDMS continuous domain,<br />

which were confirmed by transmission electron macrography (TEM). Therefore, it<br />

is expected that MPA-g-PDMS membranes can be used effectively for the<br />

removal of organic solvents from their aqueous mixtures due to their properties of<br />

high mechanical strength, durability and processability.

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