Quantitative thermographic analysis of SKD polybutadiene

Yagfarov, M.Sh.

doi:10.1016/0032-3950(68)90005-1

Cited by 6 publications

(1 citation statement)

References 3 publications

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“…At a cis-1,4-unit content of 90 %, the maximum crystallinity of SKD is 55 % (236 K), while at 81 %, the crystallinity is insignificant. It was shown that, during photochemical isomerization, crystallization occurs when the content of trans-1,4-units is higher than 75 % [17]. However, when the content of trans-1,4-isomers is lower than 20 %, cis-1,4-structures undergo lowtemperature crystallization [18].…”

Section: Resultsmentioning

confidence: 99%

The Structure of Polybutadienes and Butadiene-Acrylonitrile Copolymers

Livanova¹,

Карпова²

2011

ChChT

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The paramagnetic probe method with the use of free radicals of different dimensions (2,2,6,6-tetramethyl-1-piperidinyloxy and 4-benzoate-2,2,6,6-tetramethyl-1piperidinyloxy) has been employed to study the effect of the isomeric composition of butadiene units in polybutadienes and butadiene-acrylonitrile copolymers on the number and dimensions of ordered structures. The nature of density fluctuations and defective regions, that is, the regions in which the radicals are sorbed, has been ascertained. It has been shown that the ordered regions are composed of stereoregular chain fragments, while defective regions are enriched with butadiene isomers different from those present in prevailing amounts.

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Section: Resultsmentioning

confidence: 99%

The Structure of Polybutadienes and Butadiene-Acrylonitrile Copolymers

Livanova¹,

Карпова²

2011

ChChT

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Glass Transition Temperatures of Polymers

Andrews

Grulke

1999

The Wiley Database of Polymer Properties

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VI-244 4.6. Poly(benzimidazoles) VI-245 4.7. Poly(benzothiazinophenothiazines) VI-245 4.8. Poly(benzothiazoles) VI-245 4.9. Poly(benzoxazlnes) VI-245 4.10. Poly(benzoxazoles) VI-245 4.11. Poly(carboranes) VI-245 4.12. Poly(dibenzofurans) VI-246 4.13. Poly(dioxoisoindolines) VI-246 4.14. Poly(fluoresceins) VI-247 4.15. Poly(furan tetracarboxylic acid diimides) VI-247 4.16. Poly(oxabicyclononanes) VI-247 4.17. Poly(oxadiazoles) VI-248 4.18. Poly(oxindoles) VI-248 4.19. Poly(oxoisoindolines) VI-248 4.20. Poly(phthalazines) VI-248 4.21. Poly(phthalides) VI-248 4.22. Poly(piperazines) VI-248 4.23. Poly(piperidines) VI-249 4.24. Poly(pyrazinoquinoxalines) VI-249 4.25. Poly(pyrazoles) VI-249 4.26. Poly(pyridazines) VI-249 4.27. Poly(pyridines) VI-249 4.28. Poly(pyromellitimides) VI-249 4.29. Poly(pyrrolidines) VI-250 4.30. Poly(quinones) VI-250 4.31. Poly(quinoxalines) VI-250 4.32. Poly(triazines) VI-252 4.33. Poly(triazoles) VI-252 Table 5. Copolymers VI-252 G. References VI-253 A. INTRODUCTIONAmorphous (noncrystalline) polymeric solids are either glasses or rubbers. A glassy polymer lacks long range order, and is below the temperature at which molecular motions take place on the time scale of the experiment. A rubbery polymer is above the temperature at which molecular motions take place on the time scale of the experiment. The glass transition temperature, T g , is the critical temperature that separates glassy behavior from rubbery behavior. Many amorphous solids, including polymers, organic liquids, biomaterials, some metals and alloys, and inorganic oxide glasses, exhibit glass transition temperatures. The dramatic change in the local movement of polymer chains at T g leads to large changes in a host of physical properties. These properties include density, specific heat, mechanical modulus, mechanical energy absorption, dielectric coefficients, acoustical properties, viscosity, and the rate of gas or liquid diffusion through the polymer, to name a few. Any of these properties can be used, at least in a crude manner, to determine T g . References page VI -253 Specific volume Gl assCrystal l i zati on vol ume change Li qui d

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