Hydration dynamics in aqueous Pluronic P123 solution: Concentration and temperature dependence

被引:8
|
作者
Mukherjee, Kallol [1 ]
Barman, Anjan [2 ]
Biswas, Ranjit [1 ]
机构
[1] SN Bose Natl Ctr Basic Sci, CBMS, JD Block,Sector 3, Kolkata 700106, India
[2] SN Bose Natl Ctr Basic Sci, CMPMS, JD Block,Sect 3, Kolkata 700106, India
来源
JOURNAL OF CHEMICAL PHYSICS | 2019年 / 151卷 / 18期
关键词
DIELECTRIC-RELAXATION SPECTROSCOPY; ANGLE NEUTRON-SCATTERING; OXIDE) BLOCK-COPOLYMER; PEO-PPO; TRIBLOCK COPOLYMERS; SOLVATION DYNAMICS; ELECTROLYTE-SOLUTIONS; AGGREGATION BEHAVIOR; MICELLAR STRUCTURE; WATER;
D O I
10.1063/1.5124526
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Here, we report the concentration (0 <= wt. % <= 30) and temperature (293 <= T/K <= 318) dependent structural and dynamical changes in an aqueous solution of a triblock copolymer (Pluronic P123) using dielectric relaxation spectroscopy (DRS), covering a frequency regime, 0.2 <= nu/GHz <= 50. Remarkable existence of slow water molecules, similar to 2 times slower than bulk type water, along with bulk-like water molecules has been detected in the present DR measurements. Differential scanning calorimetric measurements support this DR observation. The signature of the sol-gel phase transition (similar to 15.0 wt. %, 293 K) and temperature induced extensive dehydration (>60%) for P123 molecules, which are the other notable findings of the present work. Moreover, the rate of dehydration with temperature has been found to depend on the phase of the medium. However, dehydration follows a nonlinear pattern in both sol and gel phases. A subnanosecond (similar to 90 ps) component, possibly originating from the hydrogen bond relaxation dynamics of the terminal C-O-H of polymer chains, has also been observed. Published under license by AIP Publishing.
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页数:7
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