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Lester, Daniel
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Publications (2/2 displayed)
- 2019Influence of Grafting Density and Distribution on Material Properties Using Well-Defined Alkyl Functional Poly(Styrene- co-Maleic Anhydride) Architectures Synthesized by RAFTcitations
- 2019Influence of grafting density and distribution on material properties using well-defined alkyl functional poly(styrene-co-maleic anhydride) architectures synthesized by RAFTcitations
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article
Influence of Grafting Density and Distribution on Material Properties Using Well-Defined Alkyl Functional Poly(Styrene- co-Maleic Anhydride) Architectures Synthesized by RAFT
Abstract
<p>Poly(styrene-co-maleic anhydride) copolymers (PSMA) with controlled number and distribution of maleic anhydride (MAnh) units were synthesized by reversible addition-fragmentation chain transfer polymerization using chain-transfer agents (CTA) suitable for industrial scale processes. Linear- and star-shaped alternating PSMA polymers were prepared in a single-step synthesis, while a one-pot sequential chain-extension strategy was utilized to prepare diblock, multiblock, and multisite copolymer architectures. A library of grafted PSMAs with controlled density and distribution of side chains was achieved by the subsequent grafting of long aliphatic alcohol chains (C22) to the MAnh units. The influence of structure, composition, and long alkyl chain addition on PSMAs behavior in solution was studied with triple-detection size exclusion chromatography, while their thermal properties were examined by thermogravimetric analysis and differential scanning calorimetry. Overall, the side chain density and distribution did not impact the polymer conformations in solution (random coil); however, an effect on the molecular size (R<sub>h</sub>) and structure density (intrinsic viscosity) were observed. The materials density was shown to be dependent on polymer architectures as lower intrinsic viscosity was observed for the star copolymer. All the materials had similar degradation points (400 °C), while the rate of degradation showed a dependence on the MAnh content and polymeric architecture. Ultimately, the grafting of long aliphatic side chains (crystalline) onto the PSMA backbone, even at low density, was shown to drastically change the microphase ordering, as all the grafted copolymers became semicrystalline. The difference of the crystallization temperature between low density multisite materials (T<sub>c</sub>≈ 8 °C) and the high density alternating material (T<sub>c</sub>≈ 40 °C) highlights the major importance of controlling copolymer composition and structure to tune material properties.</p>