2016
DOI: 10.1016/j.psep.2016.03.005
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Comparison of using formaldehyde and carboxy methyl chitosan in preparation of Fe3O4 superparamagnetic nanoparticles-chitosan hydrogel network: Sorption behavior toward bovine serum albumin

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Cited by 46 publications
(9 citation statements)
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“…In the past few decades, many attempts have been made to create chemically crosslinked hydrogels mainly involving the use of crosslinkers such as N , N ′-methylenebisacrylamide [ 28 ], formaldehyde [ 29 ], and epichlorohydrin [ 30 ] which, nonetheless, are toxic and have to be removed from the hydrogels. Up to now, very few works have evaluated the possibility to modify biobased polymers to obtain photo-crosslinked hydrogels for water treatment and only two of them address specifically the removal of heavy metals [ 14 , 31 , 32 ].…”
Section: Introductionmentioning
confidence: 99%
“…In the past few decades, many attempts have been made to create chemically crosslinked hydrogels mainly involving the use of crosslinkers such as N , N ′-methylenebisacrylamide [ 28 ], formaldehyde [ 29 ], and epichlorohydrin [ 30 ] which, nonetheless, are toxic and have to be removed from the hydrogels. Up to now, very few works have evaluated the possibility to modify biobased polymers to obtain photo-crosslinked hydrogels for water treatment and only two of them address specifically the removal of heavy metals [ 14 , 31 , 32 ].…”
Section: Introductionmentioning
confidence: 99%
“…In the FTIR spectra ( Figure 5 ), the signals corresponding to CS, net -CS, and ( net -CS)- g -NVCL/AAc were compared to confirm the binary grafting. Firstly, in the CS spectrum, the characteristic peaks were found at 3378 cm −1 (O–H and N–H stretching), 2926 cm −1 (CH 2 stretching of the pyranose ring), 1658 cm −1 (C=O stretching) corresponding to the remaining acetamide group, and 1562 cm −1 (N–H bending) [ 31 ]. When the crosslinking was carried out, net -CS showed the same peaks but the intensity of C=O stretching and N-H bending changed because the chitosan crosslinking mechanism was carried out via Schiff’s base mechanism, in which imine groups were formed [ 6 ].…”
Section: Resultsmentioning
confidence: 99%
“…The obtained copolymers were recorded on FTIR spectroscopy in 500–4000 cm −1 as shown in Figure 1 . Peaks at 2924, 2848, 2908 and 2843 cm −1 for C-H groups (stretching, aliphatic), 1670, 1608, 1586, and 1548 cm −1 for group C-N 3500–3200 cm −1 , 1790 cm −1 for group C=O (group ester), 3500–3200 cm −1 for OH group were recorded [ 22 , 23 , 24 ]. These signals expressed the structural formula of the poly(DMA-co-AAc).…”
Section: Resultsmentioning
confidence: 99%