Reconstructing the Teaching of Activity and Activity Coefficients Centered on Intermolecular Forces: Progressive Modular Teaching Reconstruction and Practice Based on Physical Mechanism Classification

Activity and activity coefficients in chemical engineering thermodynamics feature both in-depth microscopic molecular mechanisms and intensive macroscopic engineering calculations, representing a core teaching pain point where students struggle to internalize concepts and tend to solve problems mechanically. Traditional teaching generally introduces activity coefficient models─ideal solution, Margules, Van Laar, Flory–Huggins, Wilson, NRTL, etc.─in chronological order of their development, leading to severely fragmented knowledge points, disconnected physical mechanisms, and a situation where students only apply formulas without understanding engineering model selection. This article breaks away from the outdated teaching paradigm of “listing models by era” and innovatively adopts a new perspective of classification by physical mechanisms. All activity coefficient models are uniformly categorized into four physical types: enthalpy-effect-dominated, entropy-effect-dominated, local composition microscopic enrichment, and energy–volume coupling. An integrated cognitive chain is constructed: “root of molecular forces → two core mechanisms of nonideality → progressive physical classification of models → precise selection for engineering scenarios”. Taking the typical polar–nonpolar ethanol–cyclohexane mixture system as a case throughout the course, the reform is supported by problem-oriented modular teaching, molecular dynamics microscopic visualization demonstrations, and an integrated “prediction–validation–modeling” reform of vapor–liquid equilibrium experiments. This achieves a cognitive leap for students from “memorizing formulas for numerical calculation” to “understanding mechanisms for model selection”. Teaching practice shows that the proportion of students who grasped the physical essence of activity coefficients rose from 12.2% to 88.0% after the reform and that the score rate of students’ ability to select and apply engineering models increased by 38.9%, as verified by standardized pretests and post-tests covering three dimensions, including conceptual understanding, phenomenon interpretation, and engineering application, as well as an independent sample t test. This provides a directly replicable paradigm reference for the advanced teaching reconstruction of core concepts in chemical engineering thermodynamics in universities and is mainly applicable to senior undergraduate students and graduate students majoring in chemical engineering.

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Journal
Journal of Chemical Education
Published
2026-07-16
DOI
https://doi.org/10.1021/acs.jchemed.6c00602
Primary Topic
Science Education and Pedagogy
Type
article
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article

Reconstructing the Teaching of Activity and Activity Coefficients Centered on Intermolecular Forces: Progressive Modular Teaching Reconstruction and Practice Based on Physical Mechanism Classification

Xin Yuan, Bing Lei, Shengnan Hu
Journal of Chemical Education
Science Education and Pedagogy
article

Reconstructing the Teaching of Activity and Activity Coefficients Centered on Intermolecular Forces: Progressive Modular Teaching Reconstruction and Practice Based on Physical Mechanism Classification

Xin Yuan, Bing Lei, Shengnan Hu
article en

Abstract

Activity and activity coefficients in chemical engineering thermodynamics feature both in-depth microscopic molecular mechanisms and intensive macroscopic engineering calculations, representing a core teaching pain point where students struggle to internalize concepts and tend to solve problems mechanically. Traditional teaching generally introduces activity coefficient models─ideal solution, Margules, Van Laar, Flory–Huggins, Wilson, NRTL, etc.─in chronological order of their development, leading to severely fragmented knowledge points, disconnected physical mechanisms, and a situation where students only apply formulas without understanding engineering model selection. This article breaks away from the outdated teaching paradigm of “listing models by era” and innovatively adopts a new perspective of classification by physical mechanisms. All activity coefficient models are uniformly categorized into four physical types: enthalpy-effect-dominated, entropy-effect-dominated, local composition microscopic enrichment, and energy–volume coupling. An integrated cognitive chain is constructed: “root of molecular forces → two core mechanisms of nonideality → progressive physical classification of models → precise selection for engineering scenarios”. Taking the typical polar–nonpolar ethanol–cyclohexane mixture system as a case throughout the course, the reform is supported by problem-oriented modular teaching, molecular dynamics microscopic visualization demonstrations, and an integrated “prediction–validation–modeling” reform of vapor–liquid equilibrium experiments. This achieves a cognitive leap for students from “memorizing formulas for numerical calculation” to “understanding mechanisms for model selection”. Teaching practice shows that the proportion of students who grasped the physical essence of activity coefficients rose from 12.2% to 88.0% after the reform and that the score rate of students’ ability to select and apply engineering models increased by 38.9%, as verified by standardized pretests and post-tests covering three dimensions, including conceptual understanding, phenomenon interpretation, and engineering application, as well as an independent sample t test. This provides a directly replicable paradigm reference for the advanced teaching reconstruction of core concepts in chemical engineering thermodynamics in universities and is mainly applicable to senior undergraduate students and graduate students majoring in chemical engineering.

Journal of Chemical Education
Sun Yat-sen University (CN), European Thermodynamics (United Kingdom) (GB)
Quality Education
Openalex Percentile: Top 2%
Science Education and Pedagogy
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