TY - JOUR
T1 - Additive Manufacturing of Hydrocarbon Elastomers via Simultaneous Chain Extension and Cross-linking of Hydrogenated Polybutadiene
AU - Scott, Philip J.
AU - Meenakshisundaram, Viswanath
AU - Chartrain, Nicholas A.
AU - Sirrine, Justin M.
AU - Williams, Christopher B.
AU - Long, Timothy E.
N1 - Publisher Copyright:
© 2019 American Chemical Society.
PY - 2019/4/12
Y1 - 2019/4/12
N2 - This work describes the first example of a hydrogenated polybutadiene elastomer photopolymer that addresses the process constraints of vat photopolymerization (VP) additive manufacturing. A synthetic method, which involves simultaneous thiol-ene step growth chain extension and acrylate cross-linking, addresses traditional challenges associated with this leading 3D printing platform. This facile, one-pot strategy combines the processing advantages of low molecular weight oligomers with the tunable thermomechanical and mechanical performance of higher molecular weight polymeric networks directly during printing, without requiring a postprocessing step. The addition of photoinitiator to mixtures of liquid polybutadiene oligomer and miscible dithiols enabled selective photocuring under UV exposure to form high-strain, elastic parts in comparison to neat diacrylate systems. Photolithographic printing of these photopolymers enabled the fabrication of three-dimensional, hydrocarbon elastomer objects. Photorheology elucidated curing behavior as a function of composition and UV intensity, while optical imaging and SEM revealed quality and resolution.
AB - This work describes the first example of a hydrogenated polybutadiene elastomer photopolymer that addresses the process constraints of vat photopolymerization (VP) additive manufacturing. A synthetic method, which involves simultaneous thiol-ene step growth chain extension and acrylate cross-linking, addresses traditional challenges associated with this leading 3D printing platform. This facile, one-pot strategy combines the processing advantages of low molecular weight oligomers with the tunable thermomechanical and mechanical performance of higher molecular weight polymeric networks directly during printing, without requiring a postprocessing step. The addition of photoinitiator to mixtures of liquid polybutadiene oligomer and miscible dithiols enabled selective photocuring under UV exposure to form high-strain, elastic parts in comparison to neat diacrylate systems. Photolithographic printing of these photopolymers enabled the fabrication of three-dimensional, hydrocarbon elastomer objects. Photorheology elucidated curing behavior as a function of composition and UV intensity, while optical imaging and SEM revealed quality and resolution.
KW - 3D printing
KW - additive manufacturing
KW - chain extension
KW - elastomer
KW - polybutadiene
KW - thiol-acrylate
KW - thiol-ene
KW - vat photopolymerization
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U2 - 10.1021/acsapm.8b00150
DO - 10.1021/acsapm.8b00150
M3 - Article
AN - SCOPUS:85069897849
SN - 2637-6105
VL - 1
SP - 684
EP - 690
JO - ACS Applied Polymer Materials
JF - ACS Applied Polymer Materials
IS - 4
ER -