Deviation from Equilibrium Thermodynamics of an Asphaltene Model Compound during Compression–Expansion Experiments at Fluid–Fluid Interfaces
| Autor: | Diego Pradilla, Fernando Fajardo-Rojas, Joseph R. Samaniuk, Oscar Alberto Alvarez Solano |
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| Rok vydání: | 2021 |
| Předmět: |
Langmuir
Work (thermodynamics) Materials science Relaxation (NMR) Intermolecular force Thermodynamics 02 engineering and technology Surfaces and Interfaces 010402 general chemistry 021001 nanoscience & nanotechnology Condensed Matter Physics Compression (physics) Surface pressure 01 natural sciences 0104 chemical sciences Equilibrium thermodynamics Electrochemistry General Materials Science 0210 nano-technology Spectroscopy Asphaltene |
| Zdroj: | Langmuir. 37:1799-1810 |
| ISSN: | 1520-5827 0743-7463 |
| Popis: | Asphaltenes play a crucial role in crude oil behavior, and model compounds are often used to capture, mimic, and predict certain interfacial properties. In previous works, sorption of an asphaltene model compound (C5PeC11) was studied using surface pressure isotherms, where a deviation from the expected thermodynamic behavior of the interface during decane-water and air-water compression experiments was observed but not explained. In this work, the interfacial behavior of C5PeC11 was assessed at the decane-water and the air-water interfaces using a multiscale approach that includes: compression-expansion experiments on rectangular and radial Langmuir troughs, dynamic interfacial stress relaxation, and fluorescence microscopy imaging. Connections between molecular and microscopic phenomena strongly suggest that the nonthermodynamic response can be explained through a dynamic effect whose origin lies in the predominance of intermolecular forces in C5PeC11 molecules over the mechanical compression force applied. When aggregation begins at the air-water interface, stable structures are formed, and the nonthermodynamic phenomenon is not observed in subsequent compressions. However, at the decane-water interface, the initial aggregation is not consolidated due to the effect of the oil phase on the free energy of the interface allowing the high reproducibility of the dynamic effect in subsequent compression cycles. These results highlight the need to probe interfacial systems at various length scales to adequately separate equilibrium thermodynamics from dynamic responses. |
| Databáze: | OpenAIRE |
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