posted on 2024-10-25, 20:03authored byRuoxuan Miao, Yuhan Ding, Jie Liu, Jianyu Liu, Zhirong Xin, Chunyang Bao
The development of chemically recyclable thermosetting
plastics
using dynamic covalent bonds is of great importance in the construction
of a sustainable society. However, there remains a bottleneck barrier
in fabricating dynamic covalent thermosetting plastics with simultaneously
high mechanical strength, thermal and dimensional stability, and room-temperature
chemical recyclability. Herein, a series of poly(β-amino esters)
(PBAEs)-based thermosetting plastics with high mechanical strength,
desirable dimensional stability, and room-temperature chemical recyclability
were fabricated through the aza-Michael addition reaction of bisphenol
A glycerolate diacrylate (BG), poly(propylene glycol) bis(2-aminopropyl
ether) (PPG), and adipic acid dihydrazide (ADH). By increasing the
molar ratios of ADH, the mechanical properties of PBAE-based thermosetting
plastics can be scientifically enhanced via the increase of the cross-linking
densities and hydrogen bond contents in the polymer networks. Typically,
the tensile strength and Young’s modulus of PBAE5 can be improved to 4.5 and 10.6 times of PBAE1, respectively.
Meanwhile, based on the rigid polymer network structures, PBAE-based
thermosetting plastics exhibited very small creep strain at evaluated
temperatures. More importantly, PBAEs-based thermosetting plastics
can be easily depolymerized into value-added monomers in an alkaline
aqueous solution at room temperature through the hydrolysis of β-amino
esters. Therefore, systematically tailoring the cross-linking density
and hydrogen bond contents of the polymer network is an efficient
and feasible strategy to construct mechanically strong and dimensional
stable dynamic covalent thermosetting plastics with room-temperature
chemical recyclability.