Self-consistent fractal geometry in polyampholyte hydrogels undergoing exchange and correlation charge-density

Ziyu Xing, Haibao Lu, Yongqing Fu*

*Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

Abstract

Polyampholyte (PA) hydrogels are incorporated of many internally charged polymer chains, which play an important role to influence the fractal networks and dynamic elasticity of the PA hydrogels owing to their different exchange and correlation charge-densities. Many properties of the PA hydrogels, such as mechanical strength and deformation, are significantly dependent on their fractal networks. However, working principles of chemo-mechanical coupling between the fractal networks and the elasticity of PA hydrogels have not been fully understood. In this study, a self-consistent fractal geometry model integrated with a complex function is proposed to understand the constitutive relationship between dynamic networks and tailorable mechanics in the PA hydrogels. The newly developed model is uniquely incorporated with the mechanochemistry, and describes the chemical polarization reactions of charged networks and their mechanical behaviors using complex fractal functions. Based on the rubber elasticity theory, constitutive stress–strain relationships of fractal networks have been described using their elastic, conformational, repulsive and polarization free-energy functions. Finally, effectiveness of the proposed model has been verified using both finite element analysis and experimental results of the PA hydrogels reported in literature.

Original languageEnglish
Article number405302
Number of pages12
JournalJournal of Physics D: Applied Physics
Volume55
Issue number40
Early online date28 Jul 2022
DOIs
Publication statusE-pub ahead of print - 28 Jul 2022

Fingerprint

Dive into the research topics of 'Self-consistent fractal geometry in polyampholyte hydrogels undergoing exchange and correlation charge-density'. Together they form a unique fingerprint.

Cite this