Fracture-Healing Kinetics of Thermoreversible Physical Gels Quantified by Shear Rheophysical Experiments.

The fracture-healing behavior of model physically associating triblock copolymer gels was investigated with experiments coupling shear rheometry and particle tracking flow visualization. Fractured gels were allowed to rest for specific time durations, and the extent of strength recovered during the resting time was quantified as a function of temperature (20-28 °C) and gel concentration (5-6 vol %). Measured times for full strength recovery were an order of magnitude greater than characteristic relaxation times of the system. The Arrhenius activation energy for post-fracture strength recovery was found to be greater than the activation energy associated with stress relaxation, most likely due to the entropic barrier related to the healing mechanism of dangling chain reassociation with network junctions.

[1]  K. Erk,et al.  Effect of ionic crosslinking on the swelling and mechanical response of model superabsorbent polymer hydrogels for internally cured concrete , 2015 .

[2]  S. Seiffert,et al.  Relaxation and Dynamics in Transient Polymer Model Networks , 2014 .

[3]  Costantino Creton,et al.  Toughening Elastomers with Sacrificial Bonds and Watching Them Break , 2014, Science.

[4]  Jian Ping Gong,et al.  Physical hydrogels composed of polyampholytes demonstrate high toughness and viscoelasticity. , 2013, Nature materials.

[5]  Nicolas Taberlet,et al.  Ultrafast ultrasonic imaging coupled to rheometry: principle and illustration. , 2013, The Review of scientific instruments.

[6]  Kirk Czymmek,et al.  Injectable solid peptide hydrogel as a cell carrier: effects of shear flow on hydrogels and cell payload. , 2012, Langmuir : the ACS journal of surfaces and colloids.

[7]  K. Shull,et al.  Extreme strain localization and sliding friction in physically associating polymer gels. , 2012, Langmuir : the ACS journal of surfaces and colloids.

[8]  Kevin A. Cavicchi,et al.  Polyelectrolyte-Surfactant Complexes as Thermoreversible Organogelators , 2011 .

[9]  John R Hess,et al.  A self-assembling hydrophobically modified chitosan capable of reversible hemostatic action. , 2011, Biomaterials.

[10]  K. Shull,et al.  Rate-Dependent Stiffening and Strain Localization in Physically Associating Solutions , 2011 .

[11]  B. Olsen,et al.  Yielding Behavior in Injectable Hydrogels from Telechelic Proteins. , 2010, Macromolecules.

[12]  W. Frith,et al.  Relationship between molecular structure, gelation behaviour and gel properties of Fmoc-dipeptides , 2010 .

[13]  K. Shull,et al.  Strain stiffening in synthetic and biopolymer networks. , 2010, Biomacromolecules.

[14]  M. C. Stuart,et al.  Fracture and Self-Healing in a Well-Defined Self-Assembled Polymer Network , 2010 .

[15]  S. Manneville Recent experimental probes of shear banding , 2008, 0903.5389.

[16]  W. Burghardt,et al.  Self-Assembly and Stress Relaxation in Acrylic Triblock Copolymer Gels , 2007 .

[17]  P. Luckham,et al.  Syneresis and rheology of weak colloidal particle gels , 2006 .

[18]  C. Caroli,et al.  Fracture of a biopolymer gel as a viscoplastic disentanglement process , 2006, The European physical journal. E, Soft matter.

[19]  C. Caroli,et al.  Solvent control of crack dynamics in a reversible hydrogel , 2006, Nature materials.