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  4. Experimental measurements and theoretical modeling of high-pressure mass densities and interfacial tensions of carbon dioxide + n-heptane + toluene and its carbon dioxide binary systems
 
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Experimental measurements and theoretical modeling of high-pressure mass densities and interfacial tensions of carbon dioxide + n-heptane + toluene and its carbon dioxide binary systems
File(s)
heptolco2_rev.pdf (6.84 MB)
Accepted version
Author(s)
cumicheo, constanza
cartes, Marcela
Muller, EA
Mejia, andres
Type
Journal Article
Abstract
Experimental determination and theoretical predictions of the isothermal (344.15 K) mass densities and
interfacial tensions for the sys
tem carbon dioxide (CO2) with heptol (n
-
heptane + toluene) mixtures
varying liquid volume fraction compositions of toluene (0, 25, 50, 75, 100 % v/v) and over the pressure
range 0.1 to 8 MPa are reported. Measurements are carried out on a high
-
pressure dev
ice that includes a
vibrating tube densimeter and a pendant drop tensiometer. Theoretical modeling of mass densities phase
equilibria and interfacial properties (i.e., interfacial tension and interfacial concentration profiles) are
performed by employing t
he Square Gradient Theory using an extension of the Statistical Associating
Fluid Theory equation of state that accounts for ring fluids. The experimental bulk phase equilibrium
densities and interfacial tensions obtained are in very good agreement with th
e theoretical predictions.
Although there are no previous experimental data of these mixtures at the conditions explored herein, the
results follow the same trends observed from experimental data at other conditions. The combination of
experimental and mod
eling approaches provides a route to simultaneously predict phase equilibrium and
interfacial properties within acceptable statistical deviations.
For the systems and conditions studied here, we observe that the phase equilibrium of the mixtures
display z
eotropic vapor
-
liquid equilibria with positive deviations from ideal behavior. The mass bulk
densities behave ordinarily whereas the interfacial tensions decrease as the pressure or liquid mole
fraction of CO2 increases and/or the ratio toluene/heptane dec
reases. The interfacial concentration along
the interfacial region exhibits a remarkable high excess adsorption of CO2, which increases with pressure
and it is larger in n
-
heptane than in toluene. Toluene does not exhibit any special adsorption activity wh
ereas n
-
heptane displays surface activity only at low pressure in a very narrow range for the case of
CO2 + (25% n
-
heptane + 75% toluene) mixture.
Date Issued
2018-09-15
Date Acceptance
2018-04-11
Citation
Fuel, 2018, 228, pp.92-102
URI
http://hdl.handle.net/10044/1/59017
DOI
https://www.dx.doi.org/10.1016/j.fuel.2018.04.057
ISSN
0016-2361
Publisher
Elsevier
Start Page
92
End Page
102
Journal / Book Title
Fuel
Volume
228
Copyright Statement
© 2018 Elsevier Ltd. All rights reserved. This manuscript is licensed under the Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International Licence http://creativecommons.org/licenses/by-nc-nd/4.0/
Sponsor
Engineering & Physical Science Research Council (EPSRC)
Engineering & Physical Science Research Council (EPSRC)
Engineering & Physical Science Research Council (EPSRC)
Grant Number
EP/E016340/1
EP/I018212/1
EP/J014958/1
Subjects
Science & Technology
Technology
Energy & Fuels
Engineering, Chemical
Engineering
High-pressure interfacial tension
High-pressure density
CO2 + hydrocarbon mixtures
Square Gradient Theory
SAFT-VR-Mie EoS
EOR
GRAINED MOLECULAR SIMULATIONS
ASSOCIATING FLUID THEORY
FORCE-FIELD PARAMETERS
ENHANCED OIL-RECOVERY
SEMI-EMPIRICAL THEORY
EQUATION-OF-STATE
PHASE-EQUILIBRIA
SURFACE-TENSION
GRADIENT THEORY
VAPOR-LIQUID
0904 Chemical Engineering
0913 Mechanical Engineering
0306 Physical Chemistry (Incl. Structural)
Energy
Publication Status
Published
Date Publish Online
2018-05-01
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