Isochronal superposition and density scaling of the intermolecular dynamics in glass-forming liquids with varying hydrogen bonding propensity

被引:30
作者
Adrjanowicz, K. [1 ,2 ]
Pionteck, J. [3 ]
Paluch, M. [1 ,4 ]
机构
[1] Silesian Univ, Inst Phys, Uniwersytecka 4, PL-40007 Katowice, Poland
[2] Adam Mickiewicz Univ, NanoBioMed Ctr, Ul Umultowska 85, PL-61614 Poznan, Poland
[3] Leibniz Inst Polymer Res Dresden, Hohe Str 6, D-01069 Dresden, Germany
[4] SMCEBI, Ul 75 Pulku Piechoty 1a, PL-41500 Chorzow, Poland
关键词
MOLECULAR-DYNAMICS; RELAXATION; TEMPERATURE; KETOPROFEN; TRANSITION; BEHAVIOR;
D O I
10.1039/c6ra08406k
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
We have tested the idea of thermodynamic scaling T-1 rho(gamma) and isochronal superposition in glass-forming liquids with varying propensity to form hydrogen bonds. The samples under investigation were dimeric rich ketoprofen and it is incapable of forming local hydrogen bonding structures, methylated derivative. We find that both features of viscous liquid dynamics hold better for the methylated sample and include the entire pressure-sensitive dynamics. We also show that it is possible to scale simultaneously the alpha- and secondary relaxation times in terms of T-1 rho(-gamma) approach using the same value of the gamma exponent. This is the first such clear observation reported for supercooled liquids to date. The removal of the hydrogen bonds enables these effects to be clearly identified experimentally.
引用
收藏
页码:49370 / 49375
页数:6
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