The “Nascent” Nature of High-Molecular-Weight Polymers: Molecular Dynamics Simulations of Concurrent Polymerization and Crystallization

We investigate the fundamental features that define a polymer as “nascent” by developing and analyzing a new coarse-grained molecular dynamics framework to simulate linear high-molecular-weight nascent polymers. Our model captures the simultaneous polymerization and crystallization processes that drive the formation of long chains ( ≈ 5.3 × 1 0 5 ⁡ g ⁡ m o l − 1 ), which are characterized by a lower entanglement density and a higher crystalline ratio than their counterparts synthesized from the melt state. By tuning the chain growth kinetics through the simulation parameters, we further demonstrate how the resulting semicrystalline morphology can be tailored. We eventually identify the entanglement density and the crystalline ratio as key structural descriptors to quantify the polymer nascent character, or “ nascentness ”, and propose for the first time a formal definition of this concept.

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Publication Details

Journal
Macromolecules
Published
2026-06-28
DOI
https://doi.org/10.1021/acs.macromol.5c03629
Primary Topic
Polymer crystallization and properties
Type
article
Field-Weighted Citation Impact
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article

The “Nascent” Nature of High-Molecular-Weight Polymers: Molecular Dynamics Simulations of Concurrent Polymerization and Crystallization

Olivier Lame, Julien Morthomas, Guilhem P. Baeza, Mathieu Salse
Macromolecules
Polymer crystallization and properties
article

The “Nascent” Nature of High-Molecular-Weight Polymers: Molecular Dynamics Simulations of Concurrent Polymerization and Crystallization

Olivier Lame, Julien Morthomas, Guilhem P. Baeza, Mathieu Salse
article en

Abstract

We investigate the fundamental features that define a polymer as “nascent” by developing and analyzing a new coarse-grained molecular dynamics framework to simulate linear high-molecular-weight nascent polymers. Our model captures the simultaneous polymerization and crystallization processes that drive the formation of long chains ( ≈ 5.3 × 1 0 5 ⁡ g ⁡ m o l − 1 ), which are characterized by a lower entanglement density and a higher crystalline ratio than their counterparts synthesized from the melt state. By tuning the chain growth kinetics through the simulation parameters, we further demonstrate how the resulting semicrystalline morphology can be tailored. We eventually identify the entanglement density and the crystalline ratio as key structural descriptors to quantify the polymer nascent character, or “ nascentness ”, and propose for the first time a formal definition of this concept.

Macromolecules
Université Claude Bernard Lyon 1 (FR), Centre National de la Recherche Scientifique (FR), Institut National des Sciences Appliquées de Lyon (FR), Université Jean Monnet (FR)
Openalex Percentile: Top 14%
Polymer crystallization and properties
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