Please use this identifier to cite or link to this item: https://doi.org/10.3390/polym10040358
DC FieldValue
dc.titlePhase transition effects on mechanical properties of NIPA hydrogel
dc.contributor.authorZhang, N
dc.contributor.authorZheng, S
dc.contributor.authorPan, Z
dc.contributor.authorLiu, Z
dc.date.accessioned2020-10-20T08:53:56Z
dc.date.available2020-10-20T08:53:56Z
dc.date.issued2018
dc.identifier.citationZhang, N, Zheng, S, Pan, Z, Liu, Z (2018). Phase transition effects on mechanical properties of NIPA hydrogel. Polymers 10 (4) : 358. ScholarBank@NUS Repository. https://doi.org/10.3390/polym10040358
dc.identifier.issn20734360
dc.identifier.urihttps://scholarbank.nus.edu.sg/handle/10635/178250
dc.description.abstractDue to its excellent temperature sensitivity, the Poly(N-isopropylacrylamide) (NIPA) hydrogel has attracted great interest for a wide variety of applications in tissue engineering and regenerative medicine. NIPA hydrogel undergoes an abrupt volume phase transition at a lower critical solution temperature (LCST) of 30-35°C. However, the mechanical behaviors of NIPA hydrogel induced by phase transition are still not well understood. In this study, phase transition effects on mechanical properties of NIPA hydrogel are quantitatively studied from experimental studies. The mechanical properties of NIPA hydrogel with the LSCT around 35°C are systemically studied with varying temperatures (31-39°C) under a tensile test. We find that the mechanical properties of NIPA hydrogel are greatly influenced by phase transition during the tension process. The maximum nominal stress and maximum stretch above the LCST are larger than those of below the LCST. The Young's modulus of NIPA hydrogel is around 13 kPa at 31°C and approximately 28 kPa at 39°C. A dramatic increase of Young's modulus values is observed as the temperature increases through the phase transition. The samples at a temperature around the LCST are easy to rupture, because of phase coexistent. Additionally, NIPA hydrogel displays toughening behavior under a cyclic load. Furthermore, the toughening characteristic is different between the swollen state and the collapsed state. This might originate from the internal fracture process and redistribution of polymer chains during the tension process. © 2018 by the authors.
dc.rightsAttribution 4.0 International
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/
dc.sourceUnpaywall 20201031
dc.subjectAcrylic monomers
dc.subjectCyclic loads
dc.subjectElastic moduli
dc.subjectMechanical properties
dc.subjectPhase transitions
dc.subjectTensile testing
dc.subjectTissue engineering
dc.subjectToughening
dc.subjectLower critical solution temperature
dc.subjectMaximum nominal stress
dc.subjectPoly (n isopropylacrylamide)
dc.subjectTemperature increase
dc.subjectTemperature sensitivity
dc.subjectTemperature-sensitive hydrogels
dc.subjectVarying temperature
dc.subjectVolume phase transition
dc.subjectHydrogels
dc.typeArticle
dc.contributor.departmentMECHANICAL ENGINEERING
dc.description.doi10.3390/polym10040358
dc.description.sourcetitlePolymers
dc.description.volume10
dc.description.issue4
dc.description.page358
Appears in Collections:Elements
Staff Publications

Show simple item record
Files in This Item:
File Description SizeFormatAccess SettingsVersion 
10_3390_polym10040358.pdf29.7 MBAdobe PDF

OPEN

NoneView/Download

Google ScholarTM

Check

Altmetric


This item is licensed under a Creative Commons License Creative Commons