Preparation and swelling properties of poly(NIPAM) "minigel" particles prepared by inverse suspension polymerization

Citation
Pj. Dowding et al., Preparation and swelling properties of poly(NIPAM) "minigel" particles prepared by inverse suspension polymerization, J COLL I SC, 221(2), 2000, pp. 268-272
Citations number
25
Categorie Soggetti
Physical Chemistry/Chemical Physics
Journal title
JOURNAL OF COLLOID AND INTERFACE SCIENCE
ISSN journal
00219797 → ACNP
Volume
221
Issue
2
Year of publication
2000
Pages
268 - 272
Database
ISI
SICI code
0021-9797(20000115)221:2<268:PASPOP>2.0.ZU;2-M
Abstract
The characterization of temperature- and pH-sensitive poly-N-isopropylacryl amide (poly-NIPAM) microgel particles, produced by surfactant-free emulsion polymerization, has been extensively reported. In the work described here poly(NIPAM) gel particles, cross-linked with N-N'-methylenebisacrylamide (B A), have been produced using inverse suspension polymerization. These parti cles have been termed "minigels" here since they are somewhat larger than c onventional microgels, Results suggest that minigel particles are formed as a dilute suspension, within the aqueous dispersed (droplet) phase. The hyd rodynamic diameter of the minigel particles produced in this work is less t han or equal to 2.5 mu m, at 25 degrees C. The effects of temperature and p H changes, variation in cross-linker concentration, and incorporation of a charged comonomer (methacrylic acid, MAA) have been investigated. Both poly (NIPAM-BA) and poly(NIPAM-BA-MAA) minigel particles are temperature sensiti ve with swelling behavior consistent with comparable microgels, Variations in pH were found to effect the size of minigels containing ionizable groups (such as a carboxylate) by a mechanism of increased electrostatic repulsio n of charged groups with increasing pH. Overall, the production of temperat ure- and/or pH-sensitive polymers by inverse suspension polymerization resu lts in particles with swelling characteristics similar to those produced by emulsion polymerization, albeit with differing particle sizes. (C) 2000 Ac ademic Press.