The swollen networks were transferred to vials containing 50 mL of valine NCA in anh. DMF (120 mg/mL). The vials were then sealed and agitated at room temperature under vacuum for 3 days. The resulting networks were then washed with six aliquots of DI water, followed by subsequent washing with DMF (3 × 3 mL) before being sonicated in DMF (3 mL) for 30 min.
Do you have any questions about this protocol?
Post your question to gather feedback from the community. We will also invite the authors of this article to respond.