Structural relaxation as a forked road to crystallization and glass transition of vapor-deposited amorphous molecular systems

2004 ◽  
Vol 398 (4-6) ◽  
pp. 377-383 ◽  
Author(s):  
Kikujiro Ishii ◽  
Masaki Takei ◽  
Masatsugu Yamamoto ◽  
Hideyuki Nakayama
Keyword(s):  
Glass Transition ◽  
Structural Relaxation ◽  
Molecular Systems

scholarly journals Effects of Annealing on Enthalpy Recovery and Nanomechanical Behaviors of a La-Based Bulk Metallic Glass

Metals ◽  
2021 ◽  
Vol 11 (4) ◽  
pp. 579
Author(s):  
Ting Shi ◽  
Lanping Huang ◽  
Song Li
Keyword(s):  
Glass Transition ◽  
Transition Temperature ◽  
Glass Transition Temperature ◽  
Metallic Glass ◽  
Bulk Metallic Glass ◽  
Structural Relaxation ◽  
Supercooled Liquid ◽  
Supercooled Liquid Region ◽  
Liquid Region ◽  
Nanoindentation Measurement

Structural relaxation and nanomechanical behaviors of La65Al14Ni5Co5Cu9.2Ag1.8 bulk metallic glass (BMG) with a low glass transition temperature during annealing have been investigated by calorimetry and nanoindentation measurement. The enthalpy release of this metallic glass is deduced by annealing near glass transition. When annealed below glass transition temperature for 5 min, the recovered enthalpy increases with annealing temperature and reaches the maximum value at 403 K. After annealed in supercooled liquid region, the recovered enthalpy obviously decreases. For a given annealing at 393 K, the relaxation behaviors of La-based BMG can be well described by the Kohlrausch-Williams-Watts (KWW) function. The hardness, Young’s modulus, and serrated flow are sensitive to structural relaxation of this metallic glass, which can be well explained by the theory of solid-like region and liquid-like region. The decrease of ductility and the enhancement of homogeneity can be ascribed to the transformation from liquid-like region into solid-like region and the reduction of the shear transition zone (STZ).

Structural Relaxation of Vapor-Deposited Amorphous Molecular Systems: Dependence on the Deposition Temperature

2008 ◽  
Author(s):  
Kikujiro Ishii ◽  
Hideyuki Nakayama ◽  
Michio Tokuyama ◽  
Irwin Oppenheim ◽  
Hideya Nishiyama
Keyword(s):  
Structural Relaxation ◽  
Deposition Temperature ◽  
Molecular Systems

Experimental Evidence for Fast Heterogeneous Collective Structural Relaxation in a Supercooled Liquid near the Glass Transition

2000 ◽  
Vol 84 (16) ◽  
pp. 3630-3633 ◽  
Author(s):  
M. Russina ◽  
F. Mezei ◽  
R. Lechner ◽  
S. Longeville ◽  
B. Urban
Keyword(s):  
Glass Transition ◽  
Experimental Evidence ◽  
Structural Relaxation ◽  
Supercooled Liquid

scholarly journals Competition between Structural Relaxation and Crystallization in the Glass Transition Range of Random Copolymers

Polymers ◽  
2020 ◽  
Vol 12 (8) ◽  
pp. 1778
Author(s):  
Jürgen E. K. Schawe ◽  
Claus Wrana
Keyword(s):  
Glass Transition ◽  
Structural Relaxation ◽  
Random Sequence ◽  
High Sensitivity ◽  
Random Copolymers ◽  
High Time Resolution ◽  
Scanning Calorimetry ◽  
Transition Range ◽  
Glass Transition Range ◽  
And Control

Structural relaxation in polymers occurs at temperatures in the glass transition range and below. At these temperatures, crystallization is controlled by diffusion and nucleation. A sequential occurrence of structural relaxation, nucleation, and crystallization was observed for several homopolymers during annealing in the range of the glass transition. It is known from the literature that all of these processes are strongly influenced by geometrical confinements. The focus of our work is copolymers, in which the confinements are caused by the random sequence of monomer units in the polymer chain. We characterize the influence of these confinements on structure formation and relaxation in the vicinity of the glass transition. The measurements were performed with a hydrogenated nitrile-butadiene copolymer (HNBR). The kinetics of the structural relaxation and the crystallization was measured using fast differential scanning calorimetry (FDSC). This technique was selected because of the high sensitivity, the fast cooling rates, and the high time resolution. Crystallization in HNBR causes a segregation of non-crystallizable segments in the macromolecule. This yields a reduction in mobility in the vicinity of the formed crystals and as a consequence an increased amount of so-called “rigid amorphous fraction” (RAF). The RAF can be interpreted as self-assembled confinements, which limit and control the crystallization. An analysis of the crystallization and the relaxation shows that the kinetic of both is identical. This means that the Kohlrausch exponent of relaxation and the Avrami exponent of crystallization are identical. Therefore, the crystallization is not controlled by nucleation but by diffusion and is terminated by the formation of RAF.

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