Bottom-up design toward dynamically robust polyurethane elastomers. (18th March 2021)
- Record Type:
- Journal Article
- Title:
- Bottom-up design toward dynamically robust polyurethane elastomers. (18th March 2021)
- Main Title:
- Bottom-up design toward dynamically robust polyurethane elastomers
- Authors:
- Hsieh, Alex J.
Mason Wu, You-Chi
Hu, Weiguo
Mikhail, John P.
Veysset, David
Kooi, Steven E.
Nelson, Keith A.
Rutledge, Gregory C.
Swager, Timothy M. - Abstract:
- Abstract: Segmented polyurethanes exhibit versatile mechanical properties, where their outstanding resilience and toughness enable material designs with high energy-absorption capability. However, there is a lack of fundamental understanding regarding the underlying molecular pathways toward rapid dissipation of high-pressure fields. Here, we design a set of 4, 4′-methylenediphenyldiisocyanate (MDI)−butanediol (BDO)−poly(tetramethylene oxide) (PTMO)-based polyurethanes and elucidate the influence of composition on thermal transition characteristics, crystallinity, segmental dynamics of PTMO, as well as high-strain-rate impact response on the microscale. Furthermore, simulations of shock compression, performed using an isotropic, constant-stress Hugoniostat method, comparing a MDI-BDO-PTMO-based polyurethane with polyethylene models of varying crystallinity suggest that the high-rate mechanical response is dominated by a soft domain response, which in turn can be sensitive to specific interactions present in the PTMO component that are not present in PE. Graphical abstract: Image 1 Highlights: MDI-PTMO and MDI-BDO-PTMO with PTMO MW of 2900 g/mol exhibit bimodal soft-segment melting endotherms. MDI-BDO-2900 (9:1) with 9:1 [BDO]:[PTMO] ratio exhibits a higher-Tm endotherm of the MDI-BDO hard domains. 13 C ssNMR reveals insights of the PTMO crystallinity and the corresponding molecular-level dynamics. Hugoniostat simulations highlight the shock behavior dominated by the responseAbstract: Segmented polyurethanes exhibit versatile mechanical properties, where their outstanding resilience and toughness enable material designs with high energy-absorption capability. However, there is a lack of fundamental understanding regarding the underlying molecular pathways toward rapid dissipation of high-pressure fields. Here, we design a set of 4, 4′-methylenediphenyldiisocyanate (MDI)−butanediol (BDO)−poly(tetramethylene oxide) (PTMO)-based polyurethanes and elucidate the influence of composition on thermal transition characteristics, crystallinity, segmental dynamics of PTMO, as well as high-strain-rate impact response on the microscale. Furthermore, simulations of shock compression, performed using an isotropic, constant-stress Hugoniostat method, comparing a MDI-BDO-PTMO-based polyurethane with polyethylene models of varying crystallinity suggest that the high-rate mechanical response is dominated by a soft domain response, which in turn can be sensitive to specific interactions present in the PTMO component that are not present in PE. Graphical abstract: Image 1 Highlights: MDI-PTMO and MDI-BDO-PTMO with PTMO MW of 2900 g/mol exhibit bimodal soft-segment melting endotherms. MDI-BDO-2900 (9:1) with 9:1 [BDO]:[PTMO] ratio exhibits a higher-Tm endotherm of the MDI-BDO hard domains. 13 C ssNMR reveals insights of the PTMO crystallinity and the corresponding molecular-level dynamics. Hugoniostat simulations highlight the shock behavior dominated by the response of soft domains. Enabling H-bond interactions raises the rigidity of PTMO also a plausible pathway for pressure-induced dynamic stiffening. … (more)
- Is Part Of:
- Polymer. Volume 218(2021)
- Journal:
- Polymer
- Issue:
- Volume 218(2021)
- Issue Display:
- Volume 218, Issue 2021 (2021)
- Year:
- 2021
- Volume:
- 218
- Issue:
- 2021
- Issue Sort Value:
- 2021-0218-2021-0000
- Page Start:
- Page End:
- Publication Date:
- 2021-03-18
- Subjects:
- Polyurethane elastomers -- poly(tetramethylene oxide) PTMO -- Crystallinity -- Attenuated total reflectance–Fourier transform infrared (ATR–FTIR) spectroscopy -- 13C ssNMR dipolar dephasing -- Segmental dynamics -- Laser-induced particle impact test (LIPIT) -- Broadband dielectric relaxation -- Hugoniostat simulations -- Shock compressibility
Polymers -- Periodicals
Polymerization -- Periodicals
Polymères -- Périodiques
Polymérisation -- Périodiques
547.7 - Journal URLs:
- http://www.sciencedirect.com/science/journal/00323861 ↗
http://www.elsevier.com/journals ↗ - DOI:
- 10.1016/j.polymer.2021.123518 ↗
- Languages:
- English
- ISSNs:
- 0032-3861
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 6547.700000
British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store - Ingest File:
- 25241.xml