Skip to content
DraconiticResearch
Search Sources API
203,234 studies31 sourcesUpdated 45 min ago
PreprintarXiv licencearXiv

Mass-conserving growth percolation in polymer gelation

Abstract

Polymer gelation involves the emergence of a system-spanning network from growing polymer-rich domains, yet conventional percolation models typically prescribe particle size independently of material consumption. We formulate gelation as a locally mass-conserving growth-percolation process in which Voronoi capture zones define finite material reservoirs for individual nuclei. Local depletion determines the evolving supersaturation and limiting particle size, while particle contacts generate a dynamic network whose first spanning cluster defines the gel point. Three mechanisms, namely, interface-, diffusion-, and polymer-blob-controlled growth produce distinct gelation kinetics while sharing the same accessible final state. Spatial fluctuations in nucleation further generate a distribution of gelation times. The framework separates gelation from saturation and naturally captures post-gel aging as continued growth and topological maturation.

Related

  1. Synthesis of Amphiphilic Polymer Co-Networks via the Growth of a Living RAFT Network. Part II: PEGDA-Based Parent Networks
    Yihan Zhang, Jingyao Zhai, Yueru Zhao +3
    ChemRxivPreprintCC BYFull textOrganic chemistryChemRxiv
  2. Adsorption–Absorption Polymer Purification (AAPP): A Mass Transfer Strategy for Removing Residual Monomer from Synthetic Polymers
    Fairuz Z. Tasmeen, Edith Mendoza Rodriguez, Jens Ulbrich +4
    ChemRxivPreprintCC BYOrganic chemistryChemRxiv
  3. Operando Electrochemical Fluorescence Microscopy Highlights Local Buffering and Mass Transport Effects in Polymer-Promoted Electrocatalysis.
    Steffen Hardt, Katherine J Levey, Mark Aarts +3
    Journal of the American Chemical SocietyPeer-reviewedCC BYFull textElectrochemistry & energyEurope PMC
  4. Synthesis of Amphiphilic Polymer Co-Networks via the Growth of a Living RAFT Network. Part III: Effect of DMSO Content
    Jingyao Zhai, Yueru Zhao, Yihan Zhang +2
    ChemRxivPreprintCC BYFull textOrganic chemistryChemRxiv
  5. How Chemical Evidence Shapes Mechanistic Reasoning and Prediction by Large Language Models: Fine-Grained Inference in Nucleoside-Derived Supramolecular Gelation
    Ying Wang, Xi Yu
    ChemRxivPreprintLicence not statedGeneral chemistryChemRxiv
BibTeX
@misc{rege2026massconserving,
  title = {{Mass-conserving growth percolation in polymer gelation}},
  author = {Ameya Rege and Lorenz Ratke},
  howpublished = {arXiv},
  year = {2026},
  month = sep,
  doi = {10.48550/arxiv.2609.01044},
  eprint = {2609.01044},
  archivePrefix = {arXiv},
  url = {https://arxiv.org/abs/2609.01044},
}
RIS
TY  - UNPB
TI  - Mass-conserving growth percolation in polymer gelation
AU  - Ameya Rege
AU  - Lorenz Ratke
PY  - 2026
DA  - 2026/09/01
PB  - arXiv
DO  - 10.48550/arxiv.2609.01044
UR  - https://arxiv.org/abs/2609.01044
AB  - Polymer gelation involves the emergence of a system-spanning network from growing polymer-rich domains, yet conventional percolation models typically prescribe particle size independently of material consumption. We formulate gelation as a locally mass-conserving growth-percolation process in which Voronoi capture zones define finite material reservoirs for individual nuclei. Local depletion determines the evolving supersaturation and limiting particle size, while particle contacts generate a dynamic network whose first spanning cluster defines the gel point. Three mechanisms, namely, interface-, diffusion-, and polymer-blob-controlled growth produce distinct gelation kinetics while sharing the same accessible final state. Spatial fluctuations in nucleation further generate a distribution of gelation times. The framework separates gelation from saturation and naturally captures post-gel aging as continued growth and topological maturation.
ER  -