2018
DOI: 10.1007/s10853-018-2888-x
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Poly(4-vinylpyridine)-modified silica for efficient oil/water separation

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Cited by 14 publications
(18 citation statements)
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“…XPS spectra of the N (1s) region (Figure 4, left) shows a remarkable increase of the nitrogen intensity after APTES functionalization process, deconvolution of the signal shows only one component at a binding energy of 400.5 eV, which is attributed to NH2 groups [43,44], due to the chemical composition of the APTES molecule. A deconvolution The recorded Absorbance at λ = 579 nm for the Ruhemann's purple were 0.60 and 0.66 respectively, which corresponds to concentrations of (C) APTES = 6.85 × 10 −4 M for APTES@SiO 2 (200 nm) and (C) APTES = 8.55 × 10 −4 M for APTES@SiO 2 (50 nm).…”
Section: X-ray Photoelectron Spectroscopymentioning
confidence: 99%
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“…XPS spectra of the N (1s) region (Figure 4, left) shows a remarkable increase of the nitrogen intensity after APTES functionalization process, deconvolution of the signal shows only one component at a binding energy of 400.5 eV, which is attributed to NH2 groups [43,44], due to the chemical composition of the APTES molecule. A deconvolution The recorded Absorbance at λ = 579 nm for the Ruhemann's purple were 0.60 and 0.66 respectively, which corresponds to concentrations of (C) APTES = 6.85 × 10 −4 M for APTES@SiO 2 (200 nm) and (C) APTES = 8.55 × 10 −4 M for APTES@SiO 2 (50 nm).…”
Section: X-ray Photoelectron Spectroscopymentioning
confidence: 99%
“…XPS spectra of the N (1s) region (Figure 4, left) shows a remarkable increase of the nitrogen intensity after APTES functionalization process, deconvolution of the signal shows only one component at a binding energy of 400.5 eV, which is attributed to NH 2 groups [43,44], due to the chemical composition of the APTES molecule. A deconvolution study of the C 1s peak (Figure 4, right) shows three components for both cases, the first component has a binding energy (B.E.)…”
Section: X-ray Photoelectron Spectroscopymentioning
confidence: 99%
“…The modification of BPS is to functionalize the surface of the sand with bromoalkyl groups via silanization, which serves as a binder for subsequent grafting of P4VP on its surface (Figure e). Then, the P4VP polymer was grafted onto the surface of the previously silanized Sand@SiO 2 through the quaternization reaction between the bromoalkyl groups of BPS and the pyridyl groups of P4VP by heating under vacuum at 150 °C for 12 h. The grafted P4VP endows the sand surface with pH-responsive wettability. , …”
Section: Resultsmentioning
confidence: 99%
“…Then, the P4VP polymer was grafted onto the surface of the previously silanized Sand@SiO 2 through the quaternization reaction between the bromoalkyl groups of BPS and the pyridyl groups of P4VP by heating under vacuum at 150 °C for 12 h. The grafted P4VP endows the sand surface with pH-responsive wettability. [18][19][20]24 To confirm the successful chemical modifications of the sand, its surface was analyzed by XPS. The raw sand shows significant Si and O peaks around 100 eV (Si 2p), 150 eV (Si 2 s), and 530 eV (O 1 s), with possible minor C 1 s contaminants at around 285 eV (Figure 2a).…”
Section: Resultsmentioning
confidence: 99%
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