Abstract
Self-healing polymers bearing reversible and bulky urea bonds were prepared by free-radical copolymerization followed by crosslinking with diisocyanates. Linear prepolymers (PtB) were first synthesized from 2-(tert-butylamino)ethyl methacrylate (tBAEMA), methyl methacrylate (MMA), and n-butyl acrylate (BA), in a molar ratio of 1:10:10, and then crosslinked with 1,6-diisocyanatohexane (HDI) or isophorone diisocyanate (IPDI) to fabricate self-healing polymers. The reversible bonding-debonding between the tBAEMA of the polymer backbone and the isocyanate units of the crosslinker in the self-healing polymer facilitates rapid, repeatable, and water-adaptive self-healing performance, which has been extensively investigated using 1H-NMR, DSC, FT-IR, AFM, optical microscopy, and rheometric analyses. Percentage recovery (%R) and self-healing efficiency (%SHE) were also studied using tensile and single-scratch tests, respectively, and compared with a control sample. It was revealed through extensive analyses that self-healing against a single scratch can be accelerated and repeated up to a certain number of times even in water, although the self-healing polymers are not water-resistant. We also demonstrated that a self-healable tube capable of containing flowing water could be fabricated from a self-healing polymer sheet by using reversible bonding-debonding characteristics of a reversible bulky urea bond.
Original language | English |
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Pages (from-to) | 11-19 |
Number of pages | 9 |
Journal | Polymer Chemistry |
Volume | 9 |
Issue number | 1 |
DOIs | |
State | Published - 7 Jan 2018 |