“…In spectra of PEGDMA/SA (e), the peaks at 1,718 cm −1 , 1,632 cm −1 , and 1,107 cm −1 were assigned to C=O, C=C, and C–O–C groups, which belong to PEGDMA, 39 while peaks at 1,034 cm −1 , 1,603 cm −1 , and 1,415 cm −1 were assigned to O–H, symmetric, and asymmetric stretching vibration of –COO– of SA 40,41 . For spectra of KR/PEGDMA/SA (c) and PEG‐ g ‐KR/SA (d), characteristic peaks of KR, PEG, and SA can be observed, and it can be found that some peak intensities were weakened due to strong hydrogen bonding between components after blending 32,42 …”