1985
DOI: 10.1016/0032-3950(85)90031-0
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Structural transitions in polybutadiene examined by annihilation of positrons

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Cited by 2 publications
(3 citation statements)
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“…This development has caused a renaissance in applications of the PALS method in solving many actual problems of polymer physics such as the influence of chemical modification, , the effect of physical aging, , the effect of mechanical deformation, and the influence of mass, charge, and free valence transport. Most of the studies so far were carried out on plastics with a glass transition temperature, T g , above room temperature for reasons of easier experimentation; essentially less attention was focused on elastomers. As for the PALS data, a puzzling aspect is the fact that the temperature coefficients of hole expansion are about 1 order of magnitude higher than the temperature coefficients of macroscopic volume expansion. ,, In addition, some polymers with a rather complicated chemical structure exhibit complicated courses in I 3 - T dependences, ascribed to the side group mobilities ,, or to the coalescence of small holes. , Finally, in a few cases practically a saturation in the lifetime τ 3 and/or of the relative intensity I 3 was observed at temperatures well above T g not only for low molecular weight substances , but also for some epoxy polymers …”
Section: Introductionmentioning
confidence: 99%
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“…This development has caused a renaissance in applications of the PALS method in solving many actual problems of polymer physics such as the influence of chemical modification, , the effect of physical aging, , the effect of mechanical deformation, and the influence of mass, charge, and free valence transport. Most of the studies so far were carried out on plastics with a glass transition temperature, T g , above room temperature for reasons of easier experimentation; essentially less attention was focused on elastomers. As for the PALS data, a puzzling aspect is the fact that the temperature coefficients of hole expansion are about 1 order of magnitude higher than the temperature coefficients of macroscopic volume expansion. ,, In addition, some polymers with a rather complicated chemical structure exhibit complicated courses in I 3 - T dependences, ascribed to the side group mobilities ,, or to the coalescence of small holes. , Finally, in a few cases practically a saturation in the lifetime τ 3 and/or of the relative intensity I 3 was observed at temperatures well above T g not only for low molecular weight substances , but also for some epoxy polymers …”
Section: Introductionmentioning
confidence: 99%
“…Most of the studies so far were carried out on plastics with a glass transition temperature, T g , above room temperature for reasons of easier experimentation; essentially less attention was focused on elastomers. [27][28][29][30] As for the PALS data, a puzzling aspect is the fact that the temperature coefficients of hole expansion are about 1 order of magnitude higher than the temperature coefficients of macroscopic volume expansion. 13,16,20 In addition, some polymers with a rather complicated chemical structure exhibit complicated courses in I 3 -T dependences, ascribed to the side group mobilities 27,31,32 or to the coalescence of small holes.…”
Section: Introductionmentioning
confidence: 99%
“…Similar values are obtained from positron annihilation spectroscopic studies. 78 A cross -linked, nematic, liquid crystalline elastomer ( LCE ) fi lm doped with an azo -dye, Disperse Orange I (Chart 11.3 ), has been shown to exhibit a mechanical response to nonuniform illumination. 79 The LCE consists of a poly(methylsiloxane) ( PMS ) backbone with mesogenic aromatic side -chain units.…”
Section: Photochromic Guests In Polymer Hostsmentioning
confidence: 99%