Document Type

Article

Publication Date

2011

Abstract

Surfactant-free, radical precipitation copolymerization of N-isopropylmethacrylamide and the cationic co-monomer N-(3-aminopropyl) methacrylamide hydrochloride (APMH) was carried out to prepare microgels functionalized with primary amines. The morphology and hydrodynamic diameter of the microgels were characterized by atomic force microscopy and photon correlation spectroscopy, with the effect of NaCl concentration and initiator type on the microgel size and yield being investigated. When a 2,2'-azobis (2-amidinopropane) dihydrochloride (V50)-initiated reaction was carried out in pure water, relatively small microgels (similar to 160 nm in diameter) were obtained in low yield (similar to 20%). However, both the yield and size increased if the reaction was carried out in saline or by using ammonium persulfate as initiator instead of V50. Stable amine-laden microgels in the range from 160 to 950 nm in diameter with narrow size distributions were thus produced using reaction media with controlled salinity. Microgel swelling and electrophoretic mobility values as a function of pH, ionic strength, and temperature were also studied, illustrating the presence of cationic sidechains and their influence on microgel properties. Finally, the availability of the primary amine groups for post-polymerization modification was confirmed via modification with fluorescein-N-hydroxysuccinamide

Comments

This is a pre-copy-editing, author-produced PDF of an article accepted for publication in Colloid and Polymer Science, volume 289, issue 3, in 2011 following peer review. The final publication is available at Springer via DOI: 10.1007/s00396-010-2347-y.

Copyright

Springer

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