TY - JOUR
T1 - Anomalous Loss of Stiffness with Increasing Reinforcement in a Photo-Activated Nanocomposite
AU - Zhu, Hongyuan
AU - Lu, Tian Jian
AU - Xu, Feng
AU - Genin, Guy M.
AU - Lin, Min
N1 - Funding Information:
This work was supported by the National Natural Science Foundation of China (11772253, 12022206, 11532009), the Shaanxi Province Youth Talent Support Program, the Young Talent Support Plan of Xi'an Jiaotong University, the National Institutes of Health (R01AR077793).
Publisher Copyright:
© 2021 Wiley-VCH GmbH
PY - 2021/7
Y1 - 2021/7
N2 - Hydrogels are commonly doped with stiff nanoscale fillers to endow them with the strength and stiffness needed for engineering applications. Although structure–property relations for many polymer matrix nanocomposites are well established, modeling the new generation of hydrogel nanocomposites requires the study of processing–structure–property relationships because subtle differences in chemical kinetics during their synthesis can cause nearly identical hydrogels to have dramatically different mechanical properties. The authors therefore assembled a framework to relate synthesis conditions (including hydrogel and nanofiller mechanical properties and light absorbance) to gelation kinetics and mechanical properties. They validated the model against experiments on a graphene oxide (GO) doped oligo (ethylene glycol) diacrylate (OEGDA), a system in which, in apparent violation of laws from continuum mechanics, doping can reduce rather than increase the stiffness of the resulting hydrogel nanocomposites. Both model and experiment showed a key role light absorbance-dominated gelation kinetics in determining nanocomposite mechanical properties in conjunction with nanofiller reinforcement, with the nanofiller's attenuation of chemical kinetics sometimes outweighing stiffening effects to explain the observed, anomalous loss of stiffness. By bridging the chemical kinetics and mechanics of nanocomposite hydrogels, the authors' modeling framework shows promise for broad applicability to design of hydrogel nanocomposites.
AB - Hydrogels are commonly doped with stiff nanoscale fillers to endow them with the strength and stiffness needed for engineering applications. Although structure–property relations for many polymer matrix nanocomposites are well established, modeling the new generation of hydrogel nanocomposites requires the study of processing–structure–property relationships because subtle differences in chemical kinetics during their synthesis can cause nearly identical hydrogels to have dramatically different mechanical properties. The authors therefore assembled a framework to relate synthesis conditions (including hydrogel and nanofiller mechanical properties and light absorbance) to gelation kinetics and mechanical properties. They validated the model against experiments on a graphene oxide (GO) doped oligo (ethylene glycol) diacrylate (OEGDA), a system in which, in apparent violation of laws from continuum mechanics, doping can reduce rather than increase the stiffness of the resulting hydrogel nanocomposites. Both model and experiment showed a key role light absorbance-dominated gelation kinetics in determining nanocomposite mechanical properties in conjunction with nanofiller reinforcement, with the nanofiller's attenuation of chemical kinetics sometimes outweighing stiffening effects to explain the observed, anomalous loss of stiffness. By bridging the chemical kinetics and mechanics of nanocomposite hydrogels, the authors' modeling framework shows promise for broad applicability to design of hydrogel nanocomposites.
KW - gelation kinetics
KW - micromechanics
KW - nanocomposite hydrogels
KW - photo-activated nanocomposites
UR - http://www.scopus.com/inward/record.url?scp=85106703835&partnerID=8YFLogxK
U2 - 10.1002/marc.202100147
DO - 10.1002/marc.202100147
M3 - Article
C2 - 34051002
AN - SCOPUS:85106703835
SN - 1022-1336
VL - 42
JO - Macromolecular Rapid Communications
JF - Macromolecular Rapid Communications
IS - 14
M1 - 2100147
ER -