2015
DOI: 10.1016/j.aca.2014.11.022
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Preparation, characterization and application of N-methylene phosphonic acid chitosan grafted magnesia–zirconia stationary phase

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Cited by 9 publications
(5 citation statements)
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“…Thus, 1% FA-MeOH was selected as the optimal solvent composition in the following experiments. Moreover, all the phospholipids could also be completely desorbed under alkaline conditions with 1.5% ammonia (Figure S1), which conforms to adsorption–desorption conditions of the phosphate group on Lewis acidic materials reported in previous studies. From Figure B-1,C-1, the adsorption efficiencies of different lipids on Zr 6 -BTB with and without OTf modification in the optimal solvent composition are compared. The ratios of phospholipid recovery to those of other lipids (R = phospholipids/other lipids without phosphate group, selectivity to phospholipid) were 5.2–144.9 on Zr 6 OTf-BTB, whereas the selectivity to phospholipids on Zr 6 -BTB was only 0.7–2.3.…”
Section: Resultssupporting
confidence: 85%
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“…Thus, 1% FA-MeOH was selected as the optimal solvent composition in the following experiments. Moreover, all the phospholipids could also be completely desorbed under alkaline conditions with 1.5% ammonia (Figure S1), which conforms to adsorption–desorption conditions of the phosphate group on Lewis acidic materials reported in previous studies. From Figure B-1,C-1, the adsorption efficiencies of different lipids on Zr 6 -BTB with and without OTf modification in the optimal solvent composition are compared. The ratios of phospholipid recovery to those of other lipids (R = phospholipids/other lipids without phosphate group, selectivity to phospholipid) were 5.2–144.9 on Zr 6 OTf-BTB, whereas the selectivity to phospholipids on Zr 6 -BTB was only 0.7–2.3.…”
Section: Resultssupporting
confidence: 85%
“…As shown in Figure A, with the increase of the formic acid concentration in the solvent, the adsorption efficiencies of phospholipids increased. In previous studies, the increased adsorption efficiencies of phospholipid with increase of solvent acidity on other Lewis acidic materials were also reported. Moreover, besides the increase of phospholipid adsorption efficiencies, it could be found that other lipids, especially for DG and DHA, have obvious decreases in adsorption efficiencies on Zr 6 OTf-BTB with the increase of FA concentration. It could be explained by the fact that the interaction of those lipids with Zr 6 OTf-BTB is not Lewis acid–base interaction and possibly the dipolar interaction or ion exchange interaction (especially for DHA) that was weakened when more polar solvent formic acid was added or when the pH of the solvent got lower after adding formic acid.…”
Section: Resultsmentioning
confidence: 77%
“…The FTIR spectra also represented the chemical bonds that existed in NMPC ( Figure 1 a (ii)), resulting from the phosphorylation of chitosan. The NMPC spectra showed the O–H and N–H stretching bands at 3500–3200 cm −1 broadened, implying the substitution of –CH 2 PO 3 H 2 by the H atoms in the amine groups and affecting the hydrogen bonds [ 12 , 40 ]. The amine deformation peaks shifted to lower frequencies, from 1643 cm −1 and 1548 cm −1 in chitosan to 1632 cm −1 (antisymmetric deformation) and 1536 cm −1 (symmetric deformation) in NMPC; this result indicated the protonation of the chitosan amine as there was a hydrogen substitution to the methylene phosphonic groups that made it a tertiary amine and involved both peaks attributed to NH 3 + groups [ 12 , 39 ].…”
Section: Resultsmentioning
confidence: 99%
“…Chitosan, ß-(1 → 4) D-glucosamine, is a cationic amino polysaccharide which is a partly deacetylated form of chitin (extracting from the waste of exoskeleton of shrimp) [5]. Chitosan has been interested in medicine, pharmaceutical, biomedical, biological, agriculture, environment and in food technology such as, food formulations, binding, thickening, gelling, stabilizing, clarifying, antimicrobial and antioxidant agent [6][7][8].…”
Section: Introductionmentioning
confidence: 99%