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Additive Manufacturing of Hydrocarbon Elastomers via Simultaneous Chain Extension and Cross-linking of Hydrogenated Polybutadiene AITranslate

Department of Chemistry, Virginia Tech;Department of Mechanical Engineering, Virginia Tech;Department of Mechanical Engineering, Virginia Tech;Department of Chemistry, Virginia Tech;Department of Mechanical Engineering, Virginia Tech;Department of Chemistry, Virginia Tech
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Publisher: ACS
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Abstract AITranslate

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.

KeyWords AITranslate

additive manufacturing 3D printing vat photopolymerization polybutadiene elastomer thiol−ene thiol−acrylate chain extension
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Basic Information:

DOI:https://doi.org/10.1021/acsapm.8b00150

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Citation Information:

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.

quote

GB/T 7714-2015 [1] Philip J. Scott, Viswanath Meenakshisundaram, Nicholas A. Chartrain, et al. ACS Applied Polymer Materials, 2019(1). DOI:10.1021/acsapm.8b00150.
MLA [1] Philip J. Scott, et al., ACS Applied Polymer Materials, no. 1, 2019, https://doi.org/10.1021/acsapm.8b00150.
APA [1] Philip J. Scott, Viswanath Meenakshisundaram, Nicholas A. Chartrain, Justin M. Sirrine, Christopher B. Williams, & Timothy E. Long. (2019). ACS Applied Polymer Materials(1). https://doi.org/10.1021/acsapm.8b00150
IEEE [1] Philip J. Scott, Viswanath Meenakshisundaram, Nicholas A. Chartrain, Justin M. Sirrine, Christopher B. Williams, and Timothy E. Long, ACS Applied Polymer Materials, no. 1, 2019, doi: 10.1021/acsapm.8b00150. keywords: {additive manufacturing;3D printing;vat photopolymerization;polybutadiene;elastomer;thiol−ene;thiol−acrylate;chain extension}