daohang fenxiangbox searchbox qikanlogonew daohangnew searchboxnew navrightzone footerzone paper

Polybutadiene Click Chemistry: A Rapid and Direct Method for Vat Photopolymerization AITranslate

Air Force Research Laboratory Edwards Air Force Base; Air Force Research Laboratory Edwards Air Force Base;Department of Chemistry, United States Air Force Academy; Air Force Research Laboratory Edwards Air Force Base; National Institute of Standards and Technology; Air Force Research Laboratory Edwards Air Force Base; National Institute of Standards and Technology; Air Force Research Laboratory; Air Force Research Laboratory Edwards Air Force Base; Air Force Research Laboratory Edwards Air Force Base
AITranslate
Publisher: ACS
Share Citation Information Add to Favorites

    Scan to share on WeChat or Moments

Use WeChat scan.
Share with WeChat friends or Moments

Abstract AITranslate

Thiol–ene click chemistry was utilized to cross-link unmodified commercial liquid polybutadiene (PB) and complex geometries were 3D printed using vat photopolymerization. PB homopolymer contains pendent reactive moieties inherent to its synthesis which were used as cross-linking sites in a photosensitive resin without copolymerization or postpolymerization modification of the PB to include conventional photocurable moieties such as acrylates. Thiols were found to preferentially react with pendent olefinic units, and the mechanical properties of cross-linked specimens generally behaved as expected, that is, an increase in the cross-link density led to an increase in tensile stress but a decrease in strain at break. Resins were downselected for printability and working curves were obtained, showing evidence of a “dark cure” attributed to the thiol–ene reaction’s relative insensitivity to oxygen. Objects with challenging structures were printed by using commercial digital light processing printers.

KeyWords AITranslate

polybutadiene thiol−ene click chemistry elastomer vat photopolymerization
No data

Basic Information:

DOI:https://doi.org/10.1021/acsapm.3c01601

Chinese Library Classification Number:

Citation Information:

Thiol–ene click chemistry was utilized to cross-link unmodified commercial liquid polybutadiene (PB) and complex geometries were 3D printed using vat photopolymerization. PB homopolymer contains pendent reactive moieties inherent to its synthesis which were used as cross-linking sites in a photosensitive resin without copolymerization or postpolymerization modification of the PB to include conventional photocurable moieties such as acrylates. Thiols were found to preferentially react with pendent olefinic units, and the mechanical properties of cross-linked specimens generally behaved as expected, that is, an increase in the cross-link density led to an increase in tensile stress but a decrease in strain at break. Resins were downselected for printability and working curves were obtained, showing evidence of a “dark cure” attributed to the thiol–ene reaction’s relative insensitivity to oxygen. Objects with challenging structures were printed by using commercial digital light processing printers.

quote

GB/T 7714-2015 [1] Levi M. J. Moore, Van Michael Q. Saludo, Oliver H. Grasdal, et al. ACS Applied Polymer Materials, 2023(5). DOI:10.1021/acsapm.3c01601.
MLA [1] Levi M. J. Moore, et al., ACS Applied Polymer Materials, no. 5, 2023, https://doi.org/10.1021/acsapm.3c01601.
APA [1] Levi M. J. Moore, Van Michael Q. Saludo, Oliver H. Grasdal, Kayleen M. Smith, Thomas J. Kolibaba, Jacob C. Marcischak, Jason P. Killgore, Jeremy J. Snyder, Gregory R. Yandek, & Kamran B. Ghiassi. (2023). ACS Applied Polymer Materials(5). https://doi.org/10.1021/acsapm.3c01601
IEEE [1] Levi M. J. Moore, Van Michael Q. Saludo, Oliver H. Grasdal, Kayleen M. Smith, Thomas J. Kolibaba, Jacob C. Marcischak, Jason P. Killgore, Jeremy J. Snyder, Gregory R. Yandek, and Kamran B. Ghiassi, ACS Applied Polymer Materials, no. 5, 2023, doi: 10.1021/acsapm.3c01601. keywords: {polybutadiene;thiol−ene;click chemistry;elastomer;vat photopolymerization}