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Multiblock copolymers of PPC with oligomeric PBS: with low brittle–toughness transition temperature

In order to decrease the brittle–toughness transition temperature and increase the mechanical strength of poly(propylene carbonate) (PPC), a series of multiblock copolymers of poly(propylene carbonate)-multiblock-poly(butylene succinate) (PPC-mb-PBS) are designed and synthesized. (1)H-NMR, DOSY and...

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Detalles Bibliográficos
Autores principales: Qin, Jiaxiang, Lin, Limiao, Wang, Shuanjin, Ye, Shuxian, Luo, Weikeng, Xiao, Min, Han, Dongmei, Meng, Yuezhong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society of Chemistry 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9080016/
https://www.ncbi.nlm.nih.gov/pubmed/35540779
http://dx.doi.org/10.1039/c8ra01588k
Descripción
Sumario:In order to decrease the brittle–toughness transition temperature and increase the mechanical strength of poly(propylene carbonate) (PPC), a series of multiblock copolymers of poly(propylene carbonate)-multiblock-poly(butylene succinate) (PPC-mb-PBS) are designed and synthesized. (1)H-NMR, DOSY and GPC results demonstrate the successful synthesis of PPC-mb-PBSs with designed multiblock sequence. The thermal, crystalline and mechanical properties of these PPC-mb-PBSs are evaluated by DSC, TGA, POM, tensile and tearing testing. Experiment results demonstrate that crystallinity, thermal and mechanical properties of PPC-mb-PBSs can be readily modulated by changing the composition and block length of PPC and PBS moieties. It is found that all the prepared PPC-mb-PBSs are semi-crystalline polymers with a melting temperature at 93–109 °C and a T(g) at around −40 °C. Both crystallization rate and crystallinity of the multiblock copolymers increase with increasing both PBS content and PBS block length. As a consequent, the tensile strength increases with increasing PBS/PPC block ratios at room and lower temperatures. In conclusion, the amorphous PBS phase in the block copolymers acts as soft segment, endowing PPC-mb-PBS copolymers with much better flexibility than PPC at low temperature of 273 K when PPC segments are frozen.