Calorimetric glass transition temperature and absolute heat capacity of polystyrene ultrathin films

被引:93
作者
Koh, Yung P. [1 ]
McKenna, Gregory B. [1 ]
Simon, Sindee L. [1 ]
机构
[1] Texas Tech Univ, Dept Chem Engn, Lubbock, TX 79409 USA
关键词
differential scanning calorimetry (DSC); heat capacity; glass transition; polystyrene; thin films;
D O I
10.1002/polb.21021
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
The absolute heat capacity and glass transition temperature (T-g) of unsupported ultrathin films were measured with differential scanning calorimetry with the step-scan method in an effort to further examine the thermodynamic behavior of glass-forming materials on the nanoscale. Films were stacked in layers with multiple preparation methods. The absolute heat capacity in both the glass and liquid states decreased with decreasing film thickness, and T, also decreased with decreasing film thickness. The magnitude of the Tg depression was closer to that observed for films supported on rigid substrates than that observed for freely standing films. The stacked thin films regained bulk behavior after the application of pressure at a high temperature. The effects of various preparation methods were examined, including the use of polyisobutylene as an interleaving layer between the polystyrene films. (c) 2006 Wiley Periodicals, Inc.
引用
收藏
页码:3518 / 3527
页数:10
相关论文
共 58 条
[1]   Effects of confinement on freezing and melting [J].
Alba-Simionesco, C. ;
Coasne, B. ;
Dosseh, G. ;
Dudziak, G. ;
Gubbins, K. E. ;
Radhakrishnan, R. ;
Sliwinska-Bartkowiak, M. .
JOURNAL OF PHYSICS-CONDENSED MATTER, 2006, 18 (06) :R15-R68
[2]   Effects of confinement on material behaviour at the nanometre size scale [J].
Alcoutlabi, M ;
McKenna, GB .
JOURNAL OF PHYSICS-CONDENSED MATTER, 2005, 17 (15) :R461-R524
[3]   Quantitative equivalence between polymer nanocomposites and thin polymer films [J].
Bansal, A ;
Yang, HC ;
Li, CZ ;
Cho, KW ;
Benicewicz, BC ;
Kumar, SK ;
Schadler, LS .
NATURE MATERIALS, 2005, 4 (09) :693-698
[4]   Molecular weight dependence of reductions in the glass transition temperature of thin, freely standing polymer films [J].
Dalnoki-Veress, K ;
Forrest, JA ;
Murray, C ;
Gigault, C ;
Dutcher, JR .
PHYSICAL REVIEW E, 2001, 63 (03)
[5]   Interface and surface effects on the glass transition in thin polystyrene films [J].
DeMaggio, GB ;
Frieze, WE ;
Gidley, DW ;
Zhu, M ;
Hristov, HA ;
Yee, AF .
PHYSICAL REVIEW LETTERS, 1997, 78 (08) :1524-1527
[6]   Modeling nanoporosity development in polymer films for low-k applications [J].
Doshi, P ;
Simon, S .
POLYMER ENGINEERING AND SCIENCE, 2005, 45 (05) :640-651
[7]   Probing glass transition of ultrathin polymer films at a time scale of seconds using fast differential scanning calorimetry [J].
Efremov, MY ;
Olson, EA ;
Zhang, M ;
Zhang, ZS ;
Allen, LH .
MACROMOLECULES, 2004, 37 (12) :4607-4616
[8]   Glass transition in ultrathin polymer films: Calorimetric study [J].
Efremov, MY ;
Olson, EA ;
Zhang, M ;
Zhang, Z ;
Allen, LH .
PHYSICAL REVIEW LETTERS, 2003, 91 (08)
[9]   The distribution of glass-transition temperatures in nanoscopically confined glass formers [J].
Ellison, CJ ;
Torkelson, JM .
NATURE MATERIALS, 2003, 2 (10) :695-700
[10]   Confinement and processing effects on glass transition temperature and physical aging in ultrathin polymer films: Novel fluorescence measurements [J].
Ellison, CJ ;
Kim, SD ;
Hall, DB ;
Torkelson, JM .
EUROPEAN PHYSICAL JOURNAL E, 2002, 8 (02) :155-166