2022
DOI: 10.1016/j.cej.2021.133967
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Functionalized biobased composite for metal decontamination – Insight on uranium and application to water samples collected from wells in mining areas (Sinai, Egypt)

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Cited by 49 publications
(21 citation statements)
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“…The peaks at 944 cm −1 , 882 cm −1 , and 813 cm −1 for C–H of aromatic out-of-plane bend from the MB overlapped with C–O–S bands, while the peak at 774 cm −1 for OH out-of-plane bend from polysaccharide moiety. Peaks at 660 cm −1 and 615 cm −1 for C–S stretching 42 , 73 , 74 , and that at 532 cm −1 and 443 cm −1 for the aryl sulfides 75 . These data provide strong evidence for the adsorption of MB on Se-NPs.…”
Section: Resultsmentioning
confidence: 97%
“…The peaks at 944 cm −1 , 882 cm −1 , and 813 cm −1 for C–H of aromatic out-of-plane bend from the MB overlapped with C–O–S bands, while the peak at 774 cm −1 for OH out-of-plane bend from polysaccharide moiety. Peaks at 660 cm −1 and 615 cm −1 for C–S stretching 42 , 73 , 74 , and that at 532 cm −1 and 443 cm −1 for the aryl sulfides 75 . These data provide strong evidence for the adsorption of MB on Se-NPs.…”
Section: Resultsmentioning
confidence: 97%
“…(asymm) [41], while new bands at 923 and 854 cm −1 for the TDPD and MC-TDPD, respectively, were related to the aromatic C-H bend for the heterocyclic moiety (in-plane). As Cr(VI) sorbed, most of these peaks were shifted and decreased in their intensities, especially for NH, C=O, OH, C=S, and SH (with expected tautomerization) [36,40,42,43], while after desorption for the five cycles, these bands restored as in the original sorbent before loading with metal ions, as shown in Figure S1. The specification of the most important bands is identified in Table 1.…”
Section: Ftir Analysismentioning
confidence: 93%
“…The bands at 923 and 854 cm −1 (for TDP and MC-TDP, respectively) are related to the C-H (aromatic bend) for the pyrimidine ring (in-plane). After the sorption of chromate ions, it is noticed that most of assigned peaks are shifted with decreasing intensities; these changes are specially for groups used in binding with metal ions, i.e., amine (NH), carbonyl(C=O), thion (C=S) and thiols (SH) (resulting by tautomerization) [5,64,66,67], while as desorption processes were performed (5th cycles), these peaks were noticed again with full intensities as in the original sorbent (as shown in Figure 1), while the most important assigned bands are reported in Table S1. The EI-MS shows m/z (C 4 H 4 N 2 O 2 S) calc.…”
Section: Ftir Analysismentioning
confidence: 99%