Peculiarities of crystallization in the multiblock copolymers of norbornene and cyclooctene

• Published in: European polymer journal 2017-01, Vol.86, p.143-153
• Main Authors: Shandryuk, Georgiy A., Denisova, Yulia I., Gringolts, Maria L., Krentsel, Liya B., Litmanovich, Arkadiy D., Finkelshtein, Eugene Sh, Kudryavtsev, Yaroslav V.
• Format: Article
• Language: English
• Subjects: Annealing; Catalysts; Chemical synthesis; Copolymers; Crystallinity; Crystallites; Crystallization; Decomposition reactions; Degree of blockiness; Degree of crystallinity; Differential scanning calorimetry; DSC; Fractionation; Heat measurement; Melting; Melting points; Metathesis; Multiblock copolymers; Nucleation; Polynorbornene; Polyoctenamer; Size distribution; Thermal fractionation; Triclinic crystals; X-ray diffraction
• ISSN: 0014-3057; 1873-1945
• DOI: 10.1016/j.eurpolymj.2016.11.025

[Display omitted] •Multiblock NB-COE copolymers were synthesized by cross-metathesis.•SSA thermal fractionation by DSC was carried out.•Degree of crystallinity, Tm, and mean crystallite size decrease with the conversion.•Distribution of crystallite size differs from that in PCOE and PCOE/PNB blend.•Annealing above Tm gives rise to a high-temperature endotherm. Crystallinity of statistical multiblock copolymers of norbornene and cyclooctene with nearly equimolar composition and different degrees of blockiness is studied by differential scanning calorimetry including thermal fractionation by successive self-nucleation and annealing and by X-ray diffraction. The copolymers are synthesized via recently invented reaction of polymer cross-metathesis, as a result of interchain exchange between polynorbornene and polyoctenamer in the presence of Grubbs’ catalyst of the first generation. This catalyst raises the fraction of trans-octenylene units up to more than 80% promoting formation of triclinic crystals. The copolymer degree of crystallinity and melting peak temperature decrease with the cross-metathesis conversion. At the same time the equilibrium melting temperature predicted by the Flory theory of copolymer crystallization is not much affected by the interchange reaction. Compared with the pure polyoctenamer or its equimolar blend with polynorbornene, the norborene-cyclooctene copolymers form considerably smaller crystallites. Thermal fractionation makes it possible to find their size distribution, which correlates with the average length of trans-octenylene blocks. Short annealing the multiblock copolymers above their melting points gives rise to a small but persistent endotherm 5–10 degrees above the annealing temperature, which is absent in polyoctenamer and, therefore, may indicate mixing of segregated norbornene and cyclooctene blocks.