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Molecular Dynamics Study of the Green Solvent Polyethylene Glycol with Water Impurities

Hoffmann, Markus M. ; Too, Matthew D. ; Paddock, Nathaniel A. ; Horstmann, Robin ; Kloth, Sebastian ; Vogel, Michael ; Buntkowsky, Gerd (2024)
Molecular Dynamics Study of the Green Solvent Polyethylene Glycol with Water Impurities.
In: Molecules, 2024, 29 (9)
doi: 10.26083/tuprints-00027337
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Item Type: Article
Type of entry: Secondary publication
Title: Molecular Dynamics Study of the Green Solvent Polyethylene Glycol with Water Impurities
Language: English
Date: 13 May 2024
Place of Publication: Darmstadt
Year of primary publication: 30 April 2024
Place of primary publication: Basel
Publisher: MDPI
Journal or Publication Title: Molecules
Volume of the journal: 29
Issue Number: 9
Collation: 22 Seiten
DOI: 10.26083/tuprints-00027337
Corresponding Links:
Origin: Secondary publication DeepGreen
Abstract:

Polyethylene glycol (PEG) is one of the environmentally benign solvent options for green chemistry. It readily absorbs water when exposed to the atmosphere. The Molecular Dynamics (MD) simulations of PEG200, a commercial mixture of low molecular weight polyethyelene glycol oligomers, as well as di-, tetra-, and hexaethylene glycol are presented to study the effect of added water impurities up to a weight fraction of 0.020, which covers the typical range of water impurities due to water absorption from the atmosphere. Each system was simulated a total of four times using different combinations of two force fields for the water (SPC/E and TIP4P/2005) and two force fields for the PEG and oligomer (OPLS-AA and modified OPLS-AA). The observed trends in the effects of water addition were qualitatively quite robust with respect to these force field combinations and showed that the water does not aggregate but forms hydrogen bonds at most between two water molecules. In general, the added water causes overall either no or very small and nuanced effects in the simulation results. Specifically, the obtained water RDFs are mostly identical regardless of the water content. The added water reduces oligomer hydrogen bonding interactions overall as it competes and forms hydrogen bonds with the oligomers. The loss of intramolecular oligomer hydrogen bonding is in part compensated by oligomers switching from inter- to intramolecular hydrogen bonding. The interplay of the competing hydrogen bonding interactions leads to the presence of shallow extrema with respect to the water weight fraction dependencies for densities, viscosities, and self-diffusion coefficients, in contrast to experimental measurements, which show monotonous dependencies. However, these trends are very small in magnitude and thus confirm the experimentally observed insensitivity of these physical properties to the presence of water impurities.

Uncontrolled Keywords: polyethylene glycol, ethylene glycol oligomers, water impurity, hydrogen bonding, radial distribution functions, density, self diffusion, viscosity
Identification Number: Artikel-ID: 2070
Status: Publisher's Version
URN: urn:nbn:de:tuda-tuprints-273378
Additional Information:

This article belongs to the Special Issue Green Solvents as Emerging Substitutes: Preparation, Evaluation and Application

Classification DDC: 500 Science and mathematics > 530 Physics
500 Science and mathematics > 540 Chemistry
Divisions: 05 Department of Physics > Institute for Condensed Matter Physics
07 Department of Chemistry > Eduard Zintl-Institut > Physical Chemistry
Date Deposited: 13 May 2024 13:36
Last Modified: 12 Sep 2024 06:22
SWORD Depositor: Deep Green
URI: https://tuprints.ulb.tu-darmstadt.de/id/eprint/27337
PPN: 521325498
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