TY - JOUR
T1 - Microphase Separation Effects on Surface Scratch-Healing and Thermo-Mechanical Properties of Self-Healing Copolymers with Dynamic Covalent Bonds
AU - Han, Kyung Rok
AU - Saddique, Anam
AU - Lyu, Jihong
AU - Kim, Jin Chul
AU - Cheong, In Woo
N1 - Publisher Copyright:
© 2024 American Chemical Society.
PY - 2024/7/12
Y1 - 2024/7/12
N2 - Achieving an equilibrium between the self-healing performance and thermo-mechanical properties of polymers is crucial, but exploration of the properties of self-healing polymers based on dynamic covalent bonding (DCB) in microphase-separated polymer structures remains underinvestigated. This study examines the effects of microphase separation on the self-healing and thermo-mechanical properties of a poly(dimethylsiloxane), bis(3-aminopropyl) terminated, herein denoted as PDMS, cross-linked acrylic copolymer with hindered urea bonds (HUB). This combination leverages the benefits of both acrylic copolymers and PDMS. The phase separation of the self-healing copolymer was manipulated by using solvent blending and thermal annealing methods. Two PDMSs with different molecular lengths were used to study the effects on domain size and cross-linking density. It was confirmed that solvent blending curtails microphase separation, leading to crushed nanodomains of PDMS, while thermal annealing promotes clear microphase separation with distinct nanodomains. The observations from microphase morphology, stress-strain curves, moduli, and hardness indicate a significant correlation between self-healing performance, mechanical properties, and microphase-separated structure. The self-healing capabilities of this material were validated at nano (nanoscratch test via AFM), micro (single-scratch test using optical microscopy), and macro (crosscut-healing test using UTM) scales. These findings highlight the material’s versatile nanostructures and mechanical properties, achieved through different processes, and its potential applicability in a wide range of fields.
AB - Achieving an equilibrium between the self-healing performance and thermo-mechanical properties of polymers is crucial, but exploration of the properties of self-healing polymers based on dynamic covalent bonding (DCB) in microphase-separated polymer structures remains underinvestigated. This study examines the effects of microphase separation on the self-healing and thermo-mechanical properties of a poly(dimethylsiloxane), bis(3-aminopropyl) terminated, herein denoted as PDMS, cross-linked acrylic copolymer with hindered urea bonds (HUB). This combination leverages the benefits of both acrylic copolymers and PDMS. The phase separation of the self-healing copolymer was manipulated by using solvent blending and thermal annealing methods. Two PDMSs with different molecular lengths were used to study the effects on domain size and cross-linking density. It was confirmed that solvent blending curtails microphase separation, leading to crushed nanodomains of PDMS, while thermal annealing promotes clear microphase separation with distinct nanodomains. The observations from microphase morphology, stress-strain curves, moduli, and hardness indicate a significant correlation between self-healing performance, mechanical properties, and microphase-separated structure. The self-healing capabilities of this material were validated at nano (nanoscratch test via AFM), micro (single-scratch test using optical microscopy), and macro (crosscut-healing test using UTM) scales. These findings highlight the material’s versatile nanostructures and mechanical properties, achieved through different processes, and its potential applicability in a wide range of fields.
KW - dynamic covalent bond
KW - hindered urea bond
KW - morphology
KW - phase separation
KW - self-healing
UR - http://www.scopus.com/inward/record.url?scp=85197479041&partnerID=8YFLogxK
U2 - 10.1021/acsapm.4c00925
DO - 10.1021/acsapm.4c00925
M3 - Article
AN - SCOPUS:85197479041
SN - 2637-6105
VL - 6
SP - 7512
EP - 7523
JO - ACS Applied Polymer Materials
JF - ACS Applied Polymer Materials
IS - 13
ER -