1997
DOI: 10.1023/a:1018683331603
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Cited by 43 publications
(48 citation statements)
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“…Such a positive ð@=@PÞ T relation is in keeping with the positive ð@T c =@PÞ T measured for polymers, and it is as expected from 'free volume' theories of liquid systems, including simple liquids and polymers [2,[5][6][7][8][9][10]. Generally, it is accepted that viscosity and T g should increase with pressure for a wide variety of liquids [8][9][10]. However, it has been noted that the Da term can become negative resulting in negative ð@T c =@PÞ T and (@g/@P) T relations for specific substances [11,12].…”
Section: Introduction: Polymers and 'Simple' Liquidssupporting
confidence: 70%
See 2 more Smart Citations
“…Such a positive ð@=@PÞ T relation is in keeping with the positive ð@T c =@PÞ T measured for polymers, and it is as expected from 'free volume' theories of liquid systems, including simple liquids and polymers [2,[5][6][7][8][9][10]. Generally, it is accepted that viscosity and T g should increase with pressure for a wide variety of liquids [8][9][10]. However, it has been noted that the Da term can become negative resulting in negative ð@T c =@PÞ T and (@g/@P) T relations for specific substances [11,12].…”
Section: Introduction: Polymers and 'Simple' Liquidssupporting
confidence: 70%
“…In another part of his work on pressure effects on viscosity (g) for a wide range of elemental, molecular and inorganic liquids, Bridgman found that ð@=@PÞ T had a positive slope [1]. Such a positive ð@=@PÞ T relation is in keeping with the positive ð@T c =@PÞ T measured for polymers, and it is as expected from 'free volume' theories of liquid systems, including simple liquids and polymers [2,[5][6][7][8][9][10]. Generally, it is accepted that viscosity and T g should increase with pressure for a wide variety of liquids [8][9][10].…”
Section: Introduction: Polymers and 'Simple' Liquidsmentioning
confidence: 73%
See 1 more Smart Citation
“…Even in mildly confined conditions, inorganic melts may exhibit several peculiarities. These include positive [5] or negative [6,7] dependence of viscosity on pressure, pressure-induced structural changes [8], the evolution of anisotropic flow and structural rearrangement [9,10], crystallization [11,12] and solubility of gases [13,14]. Compared to organic fluids (and particularly polymer melts), for reasons of experimental limitations, these phenomena are typically difficult to assess.…”
Section: Introductionmentioning
confidence: 99%
“…Gutzow et al [13] presented a thorough study of the kinetics of melt crystallization under applied static pressures, taking into account the thermodynamic and kinetic consequences of pressure on nucleation and crystal growth rates. They pointed out that only at very high loads (in the GPa region) can static pressure exert a real catalytic effect in the crystallization of glasses.…”
Section: Introductionmentioning
confidence: 99%