TY - JOUR
T1 - Solvent Assisted Pressure-Free Surface Welding and Reprocessing of Malleable Epoxy Polymers
AU - Shi, Qian
AU - Yu, Kai
AU - Dunn, Martin L.
AU - Wang, Tiejun
AU - Qi, H. Jerry
N1 - Publisher Copyright:
© 2016 American Chemical Society.
PY - 2016/8/9
Y1 - 2016/8/9
N2 - Covalent adaptable networks (CANs; also known as dynamic covalent networks or vitrimers) are appealing for developing simple and efficient techniques for recycling thermosetting polymers. In this paper, ethylene glycol (EG) is used as a solvent to enable pressure-free surface welding, surface repair, and recycling of a malleable epoxy where the transesterification-type bond exchange reaction (BER) imparts a dynamic nature to the covalent network. At a high temperature, the EG molecules participate in the BER, leading to dissolution of the epoxy network. If the EG is allowed to evaporate, the dissolved epoxy can re-form into a solid. The effects of EG content, temperature, and catalyst concentration on EG-assisted BERs are investigated. It is found that the amount of EG can be adjusted to tune the solution/solid transformation: An excessive amount of EG is required to dissolve the epoxy; on the other hand, a shortage of EG can shift the reaction back to re-form the polymer. Furthermore, the catalyst concentration defines the point at which dissolution initiates, while the degradation rate depends on temperature. This new EG-assisted method is further used for surface welding, surface damage repair, and powder-based reprocessing. The EG-assisted method does not require pressure and can achieve the properties of a fresh sample. It also provides potential opportunities to develop facile recycling techniques for thermosetting polymers.
AB - Covalent adaptable networks (CANs; also known as dynamic covalent networks or vitrimers) are appealing for developing simple and efficient techniques for recycling thermosetting polymers. In this paper, ethylene glycol (EG) is used as a solvent to enable pressure-free surface welding, surface repair, and recycling of a malleable epoxy where the transesterification-type bond exchange reaction (BER) imparts a dynamic nature to the covalent network. At a high temperature, the EG molecules participate in the BER, leading to dissolution of the epoxy network. If the EG is allowed to evaporate, the dissolved epoxy can re-form into a solid. The effects of EG content, temperature, and catalyst concentration on EG-assisted BERs are investigated. It is found that the amount of EG can be adjusted to tune the solution/solid transformation: An excessive amount of EG is required to dissolve the epoxy; on the other hand, a shortage of EG can shift the reaction back to re-form the polymer. Furthermore, the catalyst concentration defines the point at which dissolution initiates, while the degradation rate depends on temperature. This new EG-assisted method is further used for surface welding, surface damage repair, and powder-based reprocessing. The EG-assisted method does not require pressure and can achieve the properties of a fresh sample. It also provides potential opportunities to develop facile recycling techniques for thermosetting polymers.
UR - https://www.scopus.com/pages/publications/84981193809
U2 - 10.1021/acs.macromol.6b00858
DO - 10.1021/acs.macromol.6b00858
M3 - 文章
AN - SCOPUS:84981193809
SN - 0024-9297
VL - 49
SP - 5527
EP - 5537
JO - Macromolecules
JF - Macromolecules
IS - 15
ER -