Water hydration of polyethylene glycol dimethyl ether

Author:

Zhang Jiaqi1ORCID,Yan Yuyue1ORCID,Zhao Hongwei2ORCID,Niu Xudong1,Liu Liyuan1ORCID,Ouyang Chunmei1ORCID,Zhang Weili3ORCID

Affiliation:

1. Centre for Terahertz Waves and College of Precision Instrument and Optoeletronics Engineering, Tianjin University 1 , Tianjin 300072, China

2. Shanghai Advanced Research Institute, Chinese Academy of Sciences 2 , Shanghai 201210, China

3. School of Electrical and Computer Engineering, Oklahoma State University 3 , Stillwater, Oklahoma 74078, USA

Abstract

In this work, GHz and THz complex dielectric spectra of a polyethylene glycol dimethyl ether (2000 g/mol) aqueous solution were studied. The reorientation relaxation of water in this kind of macro-amphiphilic molecule solution can be well described by three Debye models, including under-coordinated water, bulk-like water [water molecules in a tetrahedral hydrogen bond network (bulk water) and bulk water molecules affected by hydrophobic groups], and slow hydrating water (water molecules donating hydrogen bonds to hydrophilic ether groups). The reorientation relaxation timescales of bulk-like water and slow hydration water both show increases with concentration from 9.8 to 26.7 ps and from 46.9 to 100.1 ps, respectively. By estimating the ratios of the dipole moment of slow hydration water to the dipole moment of bulk-like water, we calculated the experimental Kirkwood factors of bulk-like and slow hydrating water. The experimental Kirkwood factor of bulk-like water increased from 3.17 to 3.44 with concentrations, while the experimental Kirkwood factor of slow hydrating water roughly remained constant at 4.13 from concentrations of 15%–60%. The estimated water molecule numbers of three water components around monomers also confirm our sorting for water components.

Funder

National Natural Science Foundation of China

Publisher

AIP Publishing

Subject

Physical and Theoretical Chemistry,General Physics and Astronomy

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