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A. T. Kwan M. Yu. Efremov E. A. Olson F. Schiettekatte M. Zhang P. H. Geil L. H. Allen 《Journal of Polymer Science.Polymer Physics》2001,39(11):1237-1245
We used thin‐film differential scanning calorimetry to investigate the melting of isolated polyethylene single crystals with lamellar thicknesses of 12 ± 1 nm. We observed the melting of as few as 25 crystals. Over a wide number of crystals (25–2000 crystals), the heat of fusion was 40% larger than the bulk value. The melting temperature of the isolated single crystals was 123 ± 2 °C, 9 °C lower than that of the bulk material. We also measured the heat of fusion of quenched crystals (±15%) over a wide range of heating rates (20,000–100,000 K/s). Annealing the quenched crystals resulted in shifts in the endotherm peak by as much as 15 °C. © 2001 John Wiley & Sons, Inc. J Polym Sci B: Polym Phys 39: 1237–1245, 2001 相似文献
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Peggy Cebe 《Journal of Polymer Science.Polymer Physics》2005,43(6):629-636
This review focuses on new insights into the crystal melting transition and the amorphous glass transition of polymers that have been gained through recent advances in thermoanalytical methods. The specific heat capacity can now be studied under two extreme limits, that is, under quasi‐isothermal conditions (limit of zero heating rate) and, at the other end of the scale, under rapid heating conditions (heating rates on the order of thousands of degrees per second), made possible through nanocalorimetry. The reversible melting, and multiple reversible melting, of semicrystalline polymers is explored using quasi‐isothermal temperature modulated differential scanning calorimetry, TMDSC. The excess reversing heat capacity, above the baseline, measured under nearly isothermal conditions is attributed to locally reversible surface melting and crystallization processes that do not require molecular nucleation. Observations of double reversible melting endotherms in isotactic polystyrene suggest existence of two distinct populations of crystals, each showing locally reversible surface melting. The second subject of the review, nanocalorimetry, is utilized to study samples of small mass under conditions of very fast heating and cooling. The glass transition properties of thin amorphous polymer films are observed under adiabatic conditions. The glass transition temperature appears to be independent of film thickness, and is observed even in ultra‐thin films. Recrystallization and reorganization during rapid heating are studied by nanocalorimetry of semicrystalline polymers. The uppermost endotherm seen under normal DSC scanning of poly(ethylene terephthalate) is caused by reorganization, and vanishes under the rapid heating conditions (3000K/s) provided by nanocalorimetry. © 2005 Wiley Periodicals, Inc. J Polym Sci Part B: Polym Phys 43: 629–636, 2005 相似文献
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Andres Krumme Arja Lehtinen Sergey Adamovsky Christoph Schick Jaan Roots Anti Viikna 《Journal of Polymer Science.Polymer Physics》2008,46(15):1577-1588
Effect of molar mass distribution (MMD) and composition distribution (CD) on crystallization behavior of linear low‐density polyethylene materials at moderate and high supercooling was studied using differential scanning calorimetry, hot‐stage polarized light microscopy, small‐angle light scattering, and chip nanocalorimetry methods. A set of uni‐ and bimodal materials having small variation in average molar mass, density, and melt flow rate, but large differences in MMD and CD, was investigated. The results indicate a clear effect of structural heterogeneity on morphology and crystallization behavior of the materials. Broader MMD and CD increased in average radius of superstructures, melting, crystallization temperatures, and isothermal crystallization rate at different supercoolings. Origin of such behavior is discussed. © 2008 Wiley Periodicals, Inc. J Polym Sci Part B: Polym Phys 46: 1577–1588, 2008 相似文献
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Martin Rosenthal David Doblas Jaime J. Hernandez Yaroslav I. Odarchenko Manfred Burghammer Emanuela Di Cola Denis Spitzer A. E. Antipov L. S. Aldoshin Dimitri A. Ivanov 《Journal of synchrotron radiation》2014,21(1):223-228
A microelectromechanical‐systems‐based calorimeter designed for use on a synchrotron nano‐focused X‐ray beamline is described. This instrument allows quantitative DC and AC calorimetric measurements over a broad range of heating/cooling rates (≤100000 K s?1) and temperature modulation frequencies (≤1 kHz). The calorimeter was used for high‐resolution thermal imaging of nanogram‐sized samples subjected to X‐ray‐induced heating. For a 46 ng indium particle, the measured temperature rise reaches ~0.2 K, and is directly correlated to the X‐ray absorption. Thermal imaging can be useful for studies of heterogeneous materials exhibiting physical and/or chemical transformations. Moreover, the technique can be extended to three‐dimensional thermal nanotomography. 相似文献
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