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DC Field | Value | Language |
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dc.contributor.advisor | Zhu, Shiping | - |
dc.contributor.advisor | Faucher, Santiago | - |
dc.contributor.author | Machado, Mark | - |
dc.date.accessioned | 2018-08-08T20:29:53Z | - |
dc.date.available | 2018-08-08T20:29:53Z | - |
dc.date.issued | 2008-06 | - |
dc.identifier.uri | http://hdl.handle.net/11375/23271 | - |
dc.description.abstract | Atom transfer radical polymerization (ATRP) is a controlled/living polymerization process used to synthesize polymers with controlled molecular weight and narrow polymer distributions. Control of these key parameters allows for the fabrication of well-defined macromolecular structures, a necessary tool for the synthesis of advanced materials. Since its discovery in 1995, ATRP has received considerable interest and widespread adoption from the academic community. Unfortunately, it faces several complex challenges which have hindered its full scale commercialization, mainly its high catalyst loadings to obtain fast reaction kinetics. One of the premises of this research project was to augment the slow reaction rates of ATRP while using extremely low catalyst concentrations. A hybrid ATRP system was employed which encompassed the fast reaction kinetics associated with conventional free radical processes, with the attractive control features of ATRP. When high free radical initiator concentrations in the range of 0.1 M to 0.2 M were used in concert with ATRP, fast reaction rates were realized, while maintaining a polymerization with living characteristics. Conversions of 81% (0.117M) and 91% (0.234M) were achieved within 2 hours as compared to typical ATRPs where achieving such conversions would take up to 24 hours. For those same free radical initiator loadings (0.117M and 0.234M) the reaction demonstrated living characteristics with molecular weight growing in a linear fashion with respect to increasing monomer conversion. Despite the high free radical initiator concentration, the polymer distribution remained relatively narrow, not exceeding a polydispersity of 1.30. Chain extension experiments from a synthesized macroinitiator were successful which demonstrated the living characteristics of the hybrid ATRP process. The aforementioned polymerizations were conducted with various copper concentrations. Catalyst concentrations as low as 16 ppm (0.234mM) were found to be effective, i.e. one catalyst mediated the growth of over 100 polymer chains, and thus saving post polymerization purification. Moreover, the expensive ligand cost could be cut dramatically through a nearly 100 time reduction in the ligand concentration for these polymerizations. A hybrid ATRP system was used as a unique method to determine termination rate coefficients of MMA at 70°C as a function of both conversion and chain length. A three dimensional composite map was developed to elucidate the coupling effects of both conversion and chain length on the termination rate coefficient over a total range of data which can be used for modelling systems of this nature. | en_US |
dc.language.iso | en | en_US |
dc.subject | termination | en_US |
dc.subject | hybrid | en_US |
dc.subject | initiation | en_US |
dc.subject | atom | en_US |
dc.subject | polymerization | en_US |
dc.subject | hybrid atom transfer | en_US |
dc.subject | radical | en_US |
dc.title | Initiation and Termination of a Hybrid Atom Transfer Radical Polymerization System | en_US |
dc.title.alternative | Initiation and Termination of a Hybrid ATRP System | en_US |
dc.type | Thesis | en_US |
dc.contributor.department | Chemical Engineering | en_US |
dc.description.degreetype | Thesis | en_US |
dc.description.degree | Master of Applied Science (MASc) | en_US |
Appears in Collections: | Digitized Open Access Dissertations and Theses |
Files in This Item:
File | Description | Size | Format | |
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machado_mark_j_2008June_masters.pdf.pdf | 13.54 MB | Adobe PDF | View/Open |
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