Hydrophilic β-cyclodextrin barrels have been tethered to a hydrophobic pulsed plasma deposited poly(4-vinylbenzyl chloride) linker layer via the Williamson ether synthesis reaction to produce an amphiphilic system that spontaneously undergoes emulsion formation to give rise to a macroporous structure. Utilization of a nonwoven polypropylene scaffold (surface area 0.5 m 2 g –1 ) yields a hierarchical 3-level porous architecture comprising β-cyclodextrin nanopores (0.78 nm), gradient polyHIPE macroporosity (3 – 5 μm), and nonwoven fibres (250 μm spacing). These high-surface-area functional materials (672 m 2 g –1 ) are shown to readily “capture” probe molecules via host–guest inclusion complex formation with the surface-tethered cyclodextrin barrels. Subsequent “release” is accomplished by altering the pH. The repeat cycling of this “capture and release” behavior has been demonstrated to exceed 90% efficiency in relation to environmentally harmful water pollutant molecules commonly associated with industrial and agricultural effluents.
No takes yet. Share an insight, caveat, or question.
Schofield et al. (2012) studied this question.