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Using Phenolic Compounds as Crosslinkers for Aminosilicones: Preperation of Silicone Elastomers with Enhanced Sustainability

dc.contributor.advisorBrook, Michael
dc.contributor.authorTamim, Khaled
dc.contributor.departmentChemistry and Chemical Biologyen_US
dc.date.accessioned2023-10-12T19:02:11Z
dc.date.available2023-10-12T19:02:11Z
dc.date.issued2023
dc.description.abstractSilicones (or polysiloxanes) are polymers consisting of an Si-O repeating unit as the backbone of the polymer, and different organic functional groups along the backbone, most commonly two methyl groups. The Si-O bond gives many unique properties to the polymers such as incredible thermal and oxidative stability, low glass transition temperatures, and low surface tensions. These properties, among many others, make silicones unique compared to carbon-based polymers and are used in many applications such as in the automotive, cosmetic, construction and electronics industry. Most silicones are used as thermosetting elastomers and cannot be recycled since thermosets cannot be melted or dissolved in solvents. Thus, they are landfilled once silicone products have met their use and are ready to be replaced. This is further worsened by the fact that most silicone elastomers are cured using metal catalysts such as platinum or tin, which are in very low abundance and typically toxic. Another means of crosslinking silicones must be utilized to meet the sustainable demands of the future. Non-covalent and covalent dynamic chemistry can offer another means of crosslinking silicones while still maintaining many of their desirable properties but adding the ability to be recycled by thermal reprocessing or specialized reagents. Catechol is an interesting molecule that can exhibit non-covalent and dynamic covalent chemistry and is the perfect candidate to replace metal-catalyzed crosslinking. A library of silicone elastomers is created by mixing catechol, closely related compounds, and amine-functional silicones with properties that are dependent on the ratios of phenol to iv amine ([ArOH]:[NH2]). Elastomers can be reprocessed by heat and can be dissolved by using simple amines, thus, reducing silicone and precious metal waste. Additionally, the silicone elastomers exhibit antioxidant activity that arises due to the radical quenching ability of the catechol. While catechol can introduce many new properties to silicone elastomers, it is toxic and hinders the sustainability profile and applications of the elastomers. Tannins are a unique class of polyphenolic compounds that are biologically derived and non-toxic, often being added to wine to help with colour and taste. Thus, commercially available tannins used in the winemaking industry are mixed with amine-functional silicones, and a set of materials is created by varying the mass loading of tannins. Up to 10% dilution of the silicone was possible while still retaining the flexibility that silicones are known for. The materials created showed many of the same properties as the catechol crosslinked materials, including recyclability, dissolution, and antioxidant properties. The tannins also impart their properties, such as flame suppression, to the materials.en_US
dc.description.degreeMaster of Science (MSc)en_US
dc.description.degreetypeThesisen_US
dc.identifier.urihttp://hdl.handle.net/11375/29028
dc.language.isoenen_US
dc.titleUsing Phenolic Compounds as Crosslinkers for Aminosilicones: Preperation of Silicone Elastomers with Enhanced Sustainabilityen_US
dc.typeThesisen_US

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