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Please use this identifier to cite or link to this item: http://hdl.handle.net/11375/7958
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dc.contributor.advisorHamielec, A.E.en_US
dc.contributor.authorDe, Somer P.en_US
dc.date.accessioned2014-06-18T16:41:21Z-
dc.date.available2014-06-18T16:41:21Z-
dc.date.created2009-05-06en_US
dc.date.issued1973-09en_US
dc.identifier.otheropendissertations/32en_US
dc.identifier.other1032en_US
dc.identifier.other841520en_US
dc.identifier.urihttp://hdl.handle.net/11375/7958-
dc.description.abstract<p>In this study uninhibited styrene, degassed under high vacuum (10ˉ⁶ mm Hg), was thermally polymerized in bulk of 10ˉ⁶ mm Hg to almost complete conversion. The samples so obtained were thermally degraded under the same high vacuum conditions at temperatures ranging between 270°C and 340°C for different time intervals over the whole range of degradation. The breakdown of the polymer, through changes in number, weight average molecular weights, polydispersity and molecular weight distribution, was investigated using gel permeation chromatography. A mechanism of degradation was sought, and the breakdown explained by a combined process of deploymerization and chain scission. Scission constants were determined and compared with the constants, obtained from a polystyrene having much larger molecular weights.</p>en_US
dc.subjectChemical Engineeringen_US
dc.subjectChemical Engineeringen_US
dc.titleThermal Degradation of Polystyreneen_US
dc.typethesisen_US
dc.contributor.departmentChemical Engineeringen_US
dc.description.degreeMaster of Engineering (ME)en_US
Appears in Collections:Open Access Dissertations and Theses

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