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Copolymerization of D,L-lactide and ε-caprolactone using tin(II) octanoate as catalysts: an insight into copolymer microstructure
Author(s) -
Sergei V. Kostjuk
Publication year - 2020
Publication title -
žurnal belorusskogo gosudarstvennogo universiteta. himiâ
Language(s) - English
Resource type - Journals
eISSN - 2617-3980
pISSN - 2520-257X
DOI - 10.33581/2520-257x-2020-2-43-49
Subject(s) - copolymer , lactide , polymer chemistry , monomer , dispersity , polymerization , caprolactone , materials science , ring opening polymerization , transesterification , catalysis , tin , chemistry , organic chemistry , polymer , composite material , metallurgy
Sn(Oct)2-catalyzed ring-opening copolymerization of D,L-lactide and e-caprolactone in bulk at 130 °C at different D,L-lactide/e-caprolactone has been studied. It was shown that independent on the initial comonomers ratio, the synthesized copolymers are enriched by D,L-lactide at the early stage of reaction indicating the formation of gradient-like copolymer. However, the intensive transesterification reaction both during the polymerization and at the monomer-starved conditions leads to the redistribution of the monomer sequences and formation of the random copolymer. The synthesized copolymers are characterized by high polydispersity (Đ > 2.0), which raises when the reaction mixture was kept under monomer-starved conditions that confirms the occurrence of transesterification. The formation of random copolymer is confirmed by single Tg value, which gradually increased with the increase of the amount of D,L-lactide in the copolymer from –48.6 °C to 33.3 °C for D,L-lactide/e-caprolactone ratio in copolymer of 20:80 and 90:10 mol/mol, respectively.

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