<p>In the wish to replace oil-based chemicals and materials with such based on biodegradable and renewable resources, this work has been performed. In a biorefinary concept, waste birch bark from paper pulp mills and timber production has been evaluated as a potential source for polyesters. </p><p>In the present thesis investigations are made on synthesis of epoxy-functionalized polyesters from the birch outer bark aliphatic suberin ω-hydroxy fatty acid, <em>cis</em>-9,10-epoxy-18-hydroxyoctadecanoic acid. Studies of accessibility and reactivity of cellulose have been performed as a first step to enable covalent attachment or grafting of the epoxy-functionalized polyesters to cellulose.<em> </em></p><p><em>Candida antarctica</em> lipase B (Novozym 435) is reported to be an efficient catalyst for condensation polymerization of <em>cis</em>-9,10-epoxy-18-hydroxyoctadecanoic acid to form poly(9,10-epoxy-18-hydroxyoctadecanoic acid) with high molecular weight (M<sub>w</sub>). Performed in toluene in the presence of molecular sieves a M<sub>w</sub> of 20000 (reaction time 68 h, M<sub>w</sub>/M<sub>n</sub> 2.2) was obtained. Performed in bulk without any drying agent a M<sub>w</sub> of 15000 was obtained at a much shorter reaction time (reaction time 3h, M<sub>w</sub>/M<sub>n</sub> 2.2). Further the same lipase has been used for succesful co-polymerizations of <em>cis</em>-9,10-epoxy-18-hydroxyoctadecanoic acid with lactones. By combining condensation and ring-opening polymerization, epoxy-functionalized linear polyesters and cyclic oligomers have been synthesized. For example, co-polymerization of <em>cis</em>-9,10-epoxy-18-hydroxy-octadecanoic acid and ε-caprolactone performed in toluene in the presence of molecular sieves gave mainly cyclic oligomers, especially at shorter reaction times. Co-polymerization performed in bulk gave linear polyesters with a M<sub>w </sub>of<sub> </sub>35000 (reaction time 24 h, M<sub>w</sub>/M<sub>n </sub>6), irrespective molecular sieves were added or not. </p><p>The epoxy-functionalized polyesters could be used for surface modification of pulp fibres and cellulose fibrils, which further can be used for production of new valuable composite materials with improved features. Knowledge of how different processing conditions affect the structure of cellulose is an important tool in the work to achieve successful grafting of produced polyesters to cellulose fibres/fibrils. CP/MAS <sup>13</sup>C-NMR spectroscopy has been used to study structural changes caused by the dissolving pulp process. An irreversible increase in average fibril aggregate width from raw pulp to final pulp during the process is shown. This increase in aggregate width could negatively influence the reactivity of the cellulose.</p><p> </p><p> </p>
| Identifer | oai:union.ndltd.org:UPSALLA/oai:DiVA.org:kth-10528 |
| Date | January 2009 |
| Creators | Olsson, Ann |
| Publisher | KTH, Fibre and Polymer Technology |
| Source Sets | DiVA Archive at Upsalla University |
| Language | English |
| Detected Language | English |
| Type | Licentiate thesis, comprehensive summary, text |
| Relation | Trita-CHE-Report, 1654-1081 ; 2009:21 |
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