TY - JOUR

T1 - Effects of polar fractions on interfacial and bulk properties at the oil/carbonated aqueous solution interface: Insight from molecular dynamics simulation

AU - Mirzaalian Dastjerdi, Ali

AU - Kharrat, Riyaz

AU - Niasar, Vahid

AU - Ott, Holger

N1 - Publisher Copyright: © 2023

PY - 2024/1/5

Y1 - 2024/1/5

N2 - This study utilized molecular dynamics simulations to understand the liquid/liquid interfaces in a natural environment involving carbon dioxide and various acidic components. The aim is to unravel the impact of polar fractions with various chemical structures and functional groups, namely benzoic acid, decanoic acid, phenol, and decanol, on the interfacial phenomena of the oleic phase (decane) in contact with water or CO 2-rich water at the molecular resolution. The findings indicate that carbon dioxide molecules enrich at the decane/water interface before dissolving into the oleic phase. When polar molecules are introduced to the oleic phase, there is a competition between carbon dioxide and acidic components to accumulate at the interface. The functional hydrocarbon fractions displace carbon dioxide at the interface and bridge the oleic and aqueous phases, reducing interfacial tension. Polar components change the charge distribution of water molecules in the biphasic system, signifying that the organized water layer at the interface with the non-aqueous phase has been disrupted. In contrast to the polar molecules, the carbon dioxide tends to diffuse into the oleic phase and changes the bulk properties like oil fluidity. Accordingly, the fluidity of the decane exhibited significant enhancement by CO 2 diffusion throughout the bulk oil phase, which might lead to substantial viscosity reduction.

AB - This study utilized molecular dynamics simulations to understand the liquid/liquid interfaces in a natural environment involving carbon dioxide and various acidic components. The aim is to unravel the impact of polar fractions with various chemical structures and functional groups, namely benzoic acid, decanoic acid, phenol, and decanol, on the interfacial phenomena of the oleic phase (decane) in contact with water or CO 2-rich water at the molecular resolution. The findings indicate that carbon dioxide molecules enrich at the decane/water interface before dissolving into the oleic phase. When polar molecules are introduced to the oleic phase, there is a competition between carbon dioxide and acidic components to accumulate at the interface. The functional hydrocarbon fractions displace carbon dioxide at the interface and bridge the oleic and aqueous phases, reducing interfacial tension. Polar components change the charge distribution of water molecules in the biphasic system, signifying that the organized water layer at the interface with the non-aqueous phase has been disrupted. In contrast to the polar molecules, the carbon dioxide tends to diffuse into the oleic phase and changes the bulk properties like oil fluidity. Accordingly, the fluidity of the decane exhibited significant enhancement by CO 2 diffusion throughout the bulk oil phase, which might lead to substantial viscosity reduction.

UR - http://www.scopus.com/inward/record.url?scp=85175312106&partnerID=8YFLogxK

U2 - 10.1016/j.colsurfa.2023.132660

DO - 10.1016/j.colsurfa.2023.132660

M3 - Article

VL - 680.2024

JO - Colloids and surfaces A: Physicochemical and Engineering Aspects

JF - Colloids and surfaces A: Physicochemical and Engineering Aspects

SN - 1873-4359

IS - 5 January

M1 - 132660

ER -