Charge‐selective separation and recovery of organic ions by polymeric micelles |
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Authors: | Decheng Wan Ming Jin Hongting Pu |
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Affiliation: | 1. Institute of Functional Polymers, School of Materials Science and Engineering, Tongji University, , Shanghai, 201804 People's Republic of China;2. Key Laboratory of Advanced Civil Engineering Materials (Tongji University), Ministry of Education, , Shanghai, 201804 People's Republic of China |
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Abstract: | Charge‐selective separation and recovery of organic ionic dyes by polymeric micelles (PMs) are reported. Branched polyethylenimine (PEI) functionalized with 4‐cetyloxybenzaldehyde (CBA) via Schiff‐base bonds (PEI@CBA) can extract an anionic dye from cationic contaminants, and transfer it from an aqueous phase into an apolar oil phase, and thus leading to separation. While a physical micelle of PAA@PS, with polyacrylic acid (PAA) as core and polystyrene (PS) as shell, can selectively extract a cationic dye from anionic contaminants. When polar, yet nonionic groups are eliminated from the core of a PM, charge selectivity can be significantly enhanced. Although many anionic–cationic dyes can form a poorly water‐soluble complex or precipitate, separation is still feasible with a reasonably designed PM. Finally, entrapment of a guest by a PM is found easy but release may be difficult; in this case, PEI@CBA with an acid‐sheddable shell, can recover the entrapped guest. It is also found the encapsulation of a dye is usually accompanied with dye stacking, resulting in a changed UV/vis spectrum. © 2014 Wiley Periodicals, Inc. J. Polym. Sci., Part B: Polym. Phys. 2014 , 52, 872–881 |
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Keywords: | charge‐selective core‐shell polymers host‐guest systems hyperbranched inclusion chemistry molecular recognition nanocapsule stacking selectivity separation techniques |
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