Isothermal physical aging of thin PMMA films near the glass transition temperature

被引:10
|
作者
Nam, Jung Eun [1 ]
Lee, Jong Keun [1 ]
Mauldin, Timothy C. [2 ]
机构
[1] Kumoh Natl Inst Technol, Dept Polymer Sci & Engn, Gumi 730701, South Korea
[2] Iowa State Univ, Sch Engn, Dept Mat Sci & Engn, Ames, IA 50011 USA
关键词
Physical aging; Thin film; PMMA; The glass transition temperature; POLY(METHYL METHACRYLATE); POLYMER-FILMS; RELAXATION; SURFACES;
D O I
10.1007/s00289-010-0333-7
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
Isothermal physical aging and the glass transition temperature (T (g)) of PMMA thin films were investigated by means of differential scanning calorimetry (DSC). Freestanding thin films of different molecular weights (M (w) = 120,000, 350,000, 996,000 g/mol) and film thicknesses (40-667 nm) were obtained by spin coating onto a silicon wafer substrate and then releasing the coated film using a water floating technique. The thin films were stacked in a DSC pan and isothermally aged for different aging times (t (a) = 1 and 12 h) and aging temperatures (T (a) = 105, 110, and 115 A degrees C) below but near T (g). Enthalpy relaxation (Delta H (Relax)), resulting from the isothermal physical aging, initially increased with increasing Delta T (T (g) - T (a), driving force of aging), reached a maximum value, and then decreased with further increase in Delta T. Below similar to 100 nm film thickness, Delta H (Relax) of samples aged near their T (g) (i.e., T (a) = 110 and 115 A degrees C) decreased with decreasing film thickness, indicating the suppression of physical aging. Up to 9.9 A degrees C depression in T (g) was observed for thinner films (similar to 40 nm), when compared to the thicker films (similar to 660 nm) in this study. The decrease in Delta H (Relax) with decreasing film thickness at a given T (a) appears to be associated with the reduction in T (g).
引用
收藏
页码:825 / 835
页数:11
相关论文
共 50 条
  • [21] Modeling the nonlinear PMMA behavior near glass transition temperature: application to its thermoforming
    Gilormini, P.
    Chevalier, L.
    Regnier, G.
    INTERNATIONAL CONFERENCE ON ADVANCES IN MATERIALS AND PROCESSING TECHNOLOGIES, PTS ONE AND TWO, 2010, 1315 : 179 - +
  • [22] Glass transition temperature and dynamics of α-process in thin polymer films
    Fukao, K
    Miyamoto, Y
    EUROPHYSICS LETTERS, 1999, 46 (05): : 649 - 654
  • [23] Densification and Depression in Glass Transition Temperature in Polystyrene Thin Films
    Vignaud, G.
    Chebil, M. S.
    Bal, J. K.
    Delorme, N.
    Beuvier, T.
    Grohens, Y.
    Gibaud, A.
    LANGMUIR, 2014, 30 (39) : 11599 - 11608
  • [24] Thickness dependence of the glass transition temperature in thin polymer films
    Kim, JH
    Jang, J
    Zin, WC
    LANGMUIR, 2001, 17 (09) : 2703 - 2710
  • [25] Influence of grafting on the glass transition temperature of PS thin films
    Henot, Marceau
    Chenneviere, Alexis
    Drockenmuller, Eric
    Shull, Kenneth
    Leger, Liliane
    Restagno, Frederic
    EUROPEAN PHYSICAL JOURNAL E, 2017, 40 (01):
  • [26] Glass transition temperature of (ultra-)thin polymer films
    Hsu, Hsiao-Ping
    Kremer, Kurt
    JOURNAL OF CHEMICAL PHYSICS, 2023, 159 (07):
  • [27] Influence of grafting on the glass transition temperature of PS thin films
    Marceau Hénot
    Alexis Chennevière
    Eric Drockenmuller
    Kenneth Shull
    Liliane Léger
    Frédéric Restagno
    The European Physical Journal E, 2017, 40
  • [28] Diffusional dynamics near the glass transition in amorphous polymer thin films
    Deppe, DD
    Torkelson, JM
    DISORDERED MATERIALS AND INTERFACES, 1996, 407 : 221 - 226
  • [29] Physical aging in amorphous polymers far below the glass transition temperature
    Drozdov, AD
    COMPUTATIONAL MATERIALS SCIENCE, 1999, 15 (04) : 422 - 434
  • [30] Erasure below glass-transition temperature of effect of isothermal physical aging in fully cured epoxy/amine thermosetting system
    Lee, JK
    Hwang, JY
    Gillham, JK
    JOURNAL OF APPLIED POLYMER SCIENCE, 2001, 81 (02) : 396 - 404