Plasma microcontact patterning (PμCP) and replica molding were combined to make PDMS/glass microfluidic devices with β-cyclodextrin (β-CD) patterns attached covalently on the glass surface inside microchannels.
Species-specific
isolation of microsized entities such as microplastics
and resistant bacteria from waste streams is becoming a growing environmental
challenge. By studying the on-flow immobilization of micron-sized
polystyrene particles onto functionalized silica surfaces, we ascertain
if supramolecular host–guest chemistry in aqueous solutions
can provide an alternative technology for water purification. Polystyrene
particles were modified with different degrees of adamantane (guest)
molecules, and silica surfaces were patterned with β-cyclodextrin
(β-CD, host) through microcontact printing (μCP). The
latter was exposed to solutions of these particles flowing at different
speeds, allowing us to study the effect of flow rate and multivalency
on particle binding to the surface. The obtained binding profile was
correlated with Comsol simulations. We also observed that particle
binding is directly aligned with particle’s ability to form
host–guest interactions with the β-CD-patterned surface,
as particle binding to the functionalized glass surface increased
with higher adamantane load on the polystyrene particle surface. Because
of the noncovalent character of these interactions, immobilization
is reversible and modified β-CD surfaces can be recycled, which
provides a positive outlook for their incorporation in water purification
systems.
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