Dispersion Polymerizations in Supercritical Carbon Dioxide

Joseph M. DeSimone(University of North Carolina at Chapel Hill), E. E. Maury(University of North Carolina at Chapel Hill), Yusuf́ Z. Menceloǵlu(University of North Carolina at Chapel Hill), J. B. McClain(University of North Carolina at Chapel Hill), T. J. Romack(University of North Carolina at Chapel Hill), J. R. Combes(University of North Carolina at Chapel Hill)
Science
July 15, 1994
Cited by 645

Abstract

Conventional heterogeneous dispersion polymerizations of unsaturated monomers are performed in either aqueous or organic dispersing media with the addition of interfacially active agents to stabilize the colloidal dispersion that forms. Successful stabilization of the polymer colloid during polymerization results in the formation of high molar mass polymers with high rates of polymerization. An environmentally responsible alternative to aqueous and organic dispersing media for heterogeneous dispersion polymerizations is described in which supercritical carbon dioxide (CO(2)) is used in conjunction with molecularly engineered free radical initiators and amphipathic molecules that are specifically designed to be interfacially active in CO(2). Conventional lipophilic monomers, exemplified by methyl methacrylate, can be quantitatively (>90 percent) polymerized heterogeneously to very high degrees of polymerization (>3000) in supercritical CO(2) in the presence of an added stabilizer to form kinetically stable dispersions that result in micrometer-sized particles with a narrow size distribution.


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