Nitroxide Mediated Radical Heterogeneous Polymerizations in Supercritical Carbon Dioxide
dc.contributor.author | O'Connor, Padraig | |
dc.date.accessioned | 2012-11-07T12:50:49Z | |
dc.date.available | 2013-08-08T10:32:13Z | |
dc.date.issued | 2012-03-05 | |
dc.identifier.uri | http://hdl.handle.net/10379/3036 | |
dc.description.abstract | Chapter 1 provides a general introduction to addition radical polymerizations and controlled/living radical polymerizations with an emphasis on nitroxide-mediated polymerization (NMP). The merits of supercritical carbon dioxide (scCO2) as a polymerization medium are described, focusing on heterogeneous NMP systems. Chapter 2 describes the work published in, Macromolecules 2009, 43, 914-919. The point of particle nucleation or the critical degree of polymerization (Jcrit) at which polymer chains become insoluble in the continuous medium (scCO2) has been ascertained under a variety of experimental conditions for the precipitation NMP of styrene (St) and tert-butyl acrylate (t-BA), mediated by SG1. A simple graphical model has been developed and successfully employed, whereby Jcrit can be predicted as a function of both target molecular weight and initial monomer loading. Jcrit is shown to increase linearly with increasing pressure. Chapter 3 details the work published in, J. Polym. Sci. Part A: Polym. Chem. 2011, 49, 1856-1864. Chain transfer to solvent has been investigated in the conventional radical polymerization (RP) and NMP of N-isopropylacrylamide (NIPAM) in N,N-dimethylformamide (DMF) at 120 °C. The same chain transfer to solvent constant (Ctr,S) can account for the deviation of experimental molecular weight data from theoretical, in both conventional RP and NMP. Chapter 4 gives an account of the work published in, J. Polym. Sci. Part A Polym. Chem. 2011, 49, 1719-1723. The first controlled/living inverse suspension polymerization in scCO2 is described. The NMP of NIPAM proceeded in the absence of stabilizer to high conversion with low polydispersity, affording a dry powder. The purification step entails washing with fresh scCO2, and the technique thus completely avoids of the use of environmentally damaging volatile organic compounds. Chapter 5 presents the work published in, Eur. Poly. J. 2012, doi.org/10.1016/j.eurpolymj.2012.04.011. A new preparation of thermoresponsive poly(NIPAM) containing block copolymers, involving two successive heterogeneous controlled/living NMPs in scCO2 is described. Precipitation NMPs in scCO2 give functionalised macroinitiators (MIs), and a first report of the controlled/living NMP of N,N-dimethylacrylamide in scCO2 is described. The MI initiates an inverse suspension NMP of NIPAM in scCO2. Aqueous cloud point temperature analysis for AB block copolymers show a significant dependence on poly(NIPAM) chain length. | en_US |
dc.rights | Attribution-NonCommercial-NoDerivs 3.0 Ireland | |
dc.rights.uri | https://creativecommons.org/licenses/by-nc-nd/3.0/ie/ | |
dc.subject | chain transfer | en_US |
dc.subject | Nitroxide | en_US |
dc.subject | Controlled/living | en_US |
dc.subject | Polymerizations | en_US |
dc.subject | Precipitation | en_US |
dc.subject | Inverse suspension | en_US |
dc.subject | Department of Chemistry | en_US |
dc.title | Nitroxide Mediated Radical Heterogeneous Polymerizations in Supercritical Carbon Dioxide | en_US |
dc.type | Thesis | en_US |
dc.local.note | Well defined polymer chains of specific, targeted chain length were polymerized for several monomers in the solvent, supercritical carbon dioxide. Supercritical carbon dioxide solvent was shown to be a superior medium for specific polymerizations due to physical and chemical advantages such as the absence of chain transfer to solvent. A predictive model for determining the point of particle formation in these systems was devised. | en_US |
dc.local.final | Yes | en_US |
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