Orientational effects in alkanone, alkanal or dialkyl carbonate + alkane mixtures and in alkanone + alkanone or + dialkyl carbonate systems

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Main Authors: Hevia, Fernando, González, Juan Antonio, Tristán, Cristina Alonso, de la Fuente, Isaías García, Sanz, Luis Felipe
Format: Preprint
Published: 2024
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author Hevia, Fernando
González, Juan Antonio
Tristán, Cristina Alonso
de la Fuente, Isaías García
Sanz, Luis Felipe
author_facet Hevia, Fernando
González, Juan Antonio
Tristán, Cristina Alonso
de la Fuente, Isaías García
Sanz, Luis Felipe
contents Interactions and structure of alkanone, or alkanal or dialkyl carbonate + alkane mixtures, or of 2-alkanone+ 2-alkanone, or of ketone + dialkyl carbonate systems have been investigated by means of a set of thermodynamic properties and by the application of the Flory model. The properties considered are excess molar quantities: enthalpies, $H_{\text{m}}^{\text{E}}$, volumes, $V_{\text{m}}^{\text{E}}$, or isobaric heat capacities, $C_{p \text{m}}^{\text{E}}$, and liquid-liquid equilibria. Experimental data show that alkane mixtures are characterized by rather strong dipolar interactions. In the case of systems containing ketones with the same number of C atoms and a given alkane, dipolar interactions become weaker in the sequence: aromatic > cyclic > linear. In addition, the mentioned interactions become also weaker in the order: dialkyl carbonate > linear alkanone > linear alkanal. This is an important result, as carbonates show lower effective dipole moments than the other compounds, and it suggests that the group size may be relevant when evaluating thermodynamic properties of liquid mixtures. Results on $H_{\text{m}}^{\text{E}}$ from the Flory model show that orientational effects (i.e., non-random mixing) are rather similar for systems with linear, cyclic or aromatic ketones or alkanals and alkanes. In contrast, orientational effects become weaker in dialkyl carbonate + alkane mixtures. The behaviour of 2-alkanone + 2-alkanone systems and of mixtures of longer 2-alkanones or cyclohexanone with dialkyl carbonate is close to random mixing. Larger orientational effects are encountered in solutions of carbonates and shorter 2-alkanones.
format Preprint
id arxiv_https___arxiv_org_abs_2409_10149
institution arXiv
publishDate 2024
record_format arxiv
spellingShingle Orientational effects in alkanone, alkanal or dialkyl carbonate + alkane mixtures and in alkanone + alkanone or + dialkyl carbonate systems
Hevia, Fernando
González, Juan Antonio
Tristán, Cristina Alonso
de la Fuente, Isaías García
Sanz, Luis Felipe
Chemical Physics
Interactions and structure of alkanone, or alkanal or dialkyl carbonate + alkane mixtures, or of 2-alkanone+ 2-alkanone, or of ketone + dialkyl carbonate systems have been investigated by means of a set of thermodynamic properties and by the application of the Flory model. The properties considered are excess molar quantities: enthalpies, $H_{\text{m}}^{\text{E}}$, volumes, $V_{\text{m}}^{\text{E}}$, or isobaric heat capacities, $C_{p \text{m}}^{\text{E}}$, and liquid-liquid equilibria. Experimental data show that alkane mixtures are characterized by rather strong dipolar interactions. In the case of systems containing ketones with the same number of C atoms and a given alkane, dipolar interactions become weaker in the sequence: aromatic > cyclic > linear. In addition, the mentioned interactions become also weaker in the order: dialkyl carbonate > linear alkanone > linear alkanal. This is an important result, as carbonates show lower effective dipole moments than the other compounds, and it suggests that the group size may be relevant when evaluating thermodynamic properties of liquid mixtures. Results on $H_{\text{m}}^{\text{E}}$ from the Flory model show that orientational effects (i.e., non-random mixing) are rather similar for systems with linear, cyclic or aromatic ketones or alkanals and alkanes. In contrast, orientational effects become weaker in dialkyl carbonate + alkane mixtures. The behaviour of 2-alkanone + 2-alkanone systems and of mixtures of longer 2-alkanones or cyclohexanone with dialkyl carbonate is close to random mixing. Larger orientational effects are encountered in solutions of carbonates and shorter 2-alkanones.
title Orientational effects in alkanone, alkanal or dialkyl carbonate + alkane mixtures and in alkanone + alkanone or + dialkyl carbonate systems
topic Chemical Physics
url https://arxiv.org/abs/2409.10149