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This content will become publicly available on June 13, 2023

Title: Nanoconfined Crystallization in Poly(lactic acid) (PLA) and Poly(ethylene terephthalate) (PET) Induced by Various Forms of Premelt‐Deformation
Authors:
 ;  ;  ;  ;  ;  
Award ID(s):
2017845
Publication Date:
NSF-PAR ID:
10368680
Journal Name:
Macromolecular Rapid Communications
Page Range or eLocation-ID:
Article No. 2200293
ISSN:
1022-1336
Publisher:
Wiley Blackwell (John Wiley & Sons)
Sponsoring Org:
National Science Foundation
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  1. Charge densities of cationic polymers adsorbed to lipid bilayers are estimated from second harmonic generation (SHG) spectroscopy and quartz crystal microbalance with dissipation monitoring (QCM-D) measurements. The systems surveyed included poly(vinylamine hydrochloride) (PVAm), poly(diallyldimethylammonium chloride) (PDADMAC), poly- l -lysine (PLL), and poly- l -arginine (PLR), as well as polyalcohol controls. Upon accounting for the number of positive charges associated with each polyelectrolyte, the binding constants and apparent free energies of adsorption as estimated from SHG data are comparable despite differences in molecular masses and molecular structure, with Δ G ads values of −61 ± 2, −58 ± 2, −57 ± 1, −52 ± 2, −52 ± 1 kJ mol −1 for PDADMAC 400 , PDADMAC 100 , PVAm, PLL, and PLR, respectively. Moreover, we find charge densities for polymer adlayers of approximately 0.3 C m −2 for poly(diallyldimethylammonium chloride) while those of poly(vinylamine) hydrochloride, poly- l -lysine, and poly- l -arginine are approximately 0.2 C m −2 . Time-dependent studies indicate that polycation adsorption to supported lipid bilayers is only partially reversible for most of the polymers explored. Poly(diallyldimethylammonium chloride) does not demonstrate reversible binding even over long timescales (>8 hours).