Quantifying the Effect of Spatial Confinement on the Diffusion and Nuclear Magnetic Resonance Relaxation of Water/Hydrocarbon Mixtures : A Molecular Dynamics Simulation Study

We implement molecular dynamics (MD) simulations to explore the relaxation mechanisms involved in the description of translational diffusion and rotational dynamics in water/hydrocarbon interfaces. The analysis of density profiles, self-diffusion coefficients, and nuclear magnetic resonance (NMR) re...

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Veröffentlicht in:Langmuir : the ACS journal of surfaces and colloids. - 1985. - 38(2022), 48 vom: 06. Dez., Seite 14540-14549
1. Verfasser: Amaro-Estrada, Jorge Ivan (VerfasserIn)
Weitere Verfasser: Wang, You, Torres-Verdín, Carlos
Format: Online-Aufsatz
Sprache:English
Veröffentlicht: 2022
Zugriff auf das übergeordnete Werk:Langmuir : the ACS journal of surfaces and colloids
Schlagworte:Journal Article
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520 |a We implement molecular dynamics (MD) simulations to explore the relaxation mechanisms involved in the description of translational diffusion and rotational dynamics in water/hydrocarbon interfaces. The analysis of density profiles, self-diffusion coefficients, and nuclear magnetic resonance (NMR) relaxation properties as a function of the confinement layer width and type of hydrocarbons improves the understanding of confined water properties at water/oil interfaces. Density profile fluctuations reveal the presence of water-oil interactions close to the interface. MD results show that self-diffusion coefficients and NMR relaxation times of planar and cylindrical water/oil interfaces are strongly influenced by layer thickness and geometry. Shorter (between 20 and 60%) self-diffusion coefficients and 1H NMR relaxation times were obtained for water/n-pentane, water/n-decane, and water/n-hexadecane systems than bulk diffusion coefficients. An increase in Larmor frequency from 2.3 MHz to 400 MHz shows that longitudinal relaxation time (T1) of confined oil has slightly larger differences at higher frequencies than the transverse relaxation time (T2). At 400 MHz, n-alkanes (n-pentane, n-decane, and n-hexadecane) exhibit longer relaxation times than at smaller frequency values (2.3 and 22 MHz). Analysis of spin-spin and spin-lattice times provides relevant information about inter- and intramolecular relaxation mechanisms of water and oil as a function of geometry and width of the interface layer. These MD results suggest that the strength of confinement and geometry play a vital role in the diffusion and NMR relaxation properties of water/oil interfaces 
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700 1 |a Torres-Verdín, Carlos  |e verfasserin  |4 aut 
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