2017
DOI: 10.1080/17458080.2017.1405163
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Tip and inner walls modification of single-walled carbon nanotubes (3.5 nm diameter) and preparation of polyamide/modified CNT nanocomposite reverse osmosis membrane

Abstract: (2018) Tip and inner walls modification of single-walled carbon nanotubes (3.5 nm diameter) and preparation of polyamide/modified CNT nanocomposite reverse osmosis membrane, Journal of Experimental Nanoscience, 13:1, 11-26, DOI: 10.1080/17458080.2017 ABSTRACTTo enhance the water flux and salt rejection of reverse osmosis membranes, thin film nanocomposite reverse osmosis membranes were prepared by incorporating functionalised single-walled carbon nanotubes (SWNTs). The functionalised SWNTs were obtained by c… Show more

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Cited by 14 publications
(4 citation statements)
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“…After deconvolution, high-resolution Al 2p spectra of AO (Figure S1A), PAA–AO (Figure S1B), and PAA–AO–PEI (Figure A) NC afford signals at 72.65 ± 1.11 and 74.25 ± 0.14 eV, which are indicative of Al and Al–O (Al 3+ /Al 2 O 3 ) species, respectively. , The deconvoluted high-resolution O 1s spectra of AO (Figure S1C), PAA–AO (Figure S1D), and PAA–AO–PEI NC (Figure B) show bands at 529.54 ± 0.36 and 531.3 ± 0.34 eV that may be attributed to the chemical bond of Al–O and overlapping of Al–O–Al, respectively. , The peaks of C 1s orbitals at binding energies of 283.04 ± 0.79, 285.67 ± 0.27, and 289.07 ± 0.83 eV can be assigned to C–C, C–N, and OC–OH groups, respectively, in PAA–AO (Figure S1E) and PAA–AO–PEI NC (Figure C). Furthermore, the high-resolution deconvoluted peak at 399.70 eV for N 1s orbitals in PAA–AO (Figure S1F) is the characteristic of amide (OC–N) in BAM cross-linker. However, the N 1s spectrum of PAA–AO–PEI (Figure D) was resolved into four peaks at the binding energies of 398.08, 398.69, 399.29, and 400.08 eV, which typically correspond to secondary amino, primary amino, tertiary amino, and amide, respectively. …”
Section: Resultsmentioning
confidence: 99%
“…After deconvolution, high-resolution Al 2p spectra of AO (Figure S1A), PAA–AO (Figure S1B), and PAA–AO–PEI (Figure A) NC afford signals at 72.65 ± 1.11 and 74.25 ± 0.14 eV, which are indicative of Al and Al–O (Al 3+ /Al 2 O 3 ) species, respectively. , The deconvoluted high-resolution O 1s spectra of AO (Figure S1C), PAA–AO (Figure S1D), and PAA–AO–PEI NC (Figure B) show bands at 529.54 ± 0.36 and 531.3 ± 0.34 eV that may be attributed to the chemical bond of Al–O and overlapping of Al–O–Al, respectively. , The peaks of C 1s orbitals at binding energies of 283.04 ± 0.79, 285.67 ± 0.27, and 289.07 ± 0.83 eV can be assigned to C–C, C–N, and OC–OH groups, respectively, in PAA–AO (Figure S1E) and PAA–AO–PEI NC (Figure C). Furthermore, the high-resolution deconvoluted peak at 399.70 eV for N 1s orbitals in PAA–AO (Figure S1F) is the characteristic of amide (OC–N) in BAM cross-linker. However, the N 1s spectrum of PAA–AO–PEI (Figure D) was resolved into four peaks at the binding energies of 398.08, 398.69, 399.29, and 400.08 eV, which typically correspond to secondary amino, primary amino, tertiary amino, and amide, respectively. …”
Section: Resultsmentioning
confidence: 99%
“…After 1 h, most CNTs had settled, and all CNTs had sunk to the bottom after 2 h. Besides, Figure S3 shows the dispersion of raw CNTs (without sonication–centrifugation treatment), which aggregated in a shorter time. These changes directly suggest that DOPC lipid modification enhances the dispersion and stability of CNTs in aqueous solution, which benefits the formation of a defect-free PA layer . Additionally, CNTPs exhibited a less negative charge (−15.8 mV) compared to CNTs (−28.5 mV) owing to the masking effect of the lipid modification, as shown in Figure c.…”
Section: Resultsmentioning
confidence: 86%
“…These changes directly suggest that DOPC lipid modification enhances the dispersion and stability of CNTs in aqueous solution, which benefits the formation of a defect-free PA layer. 35 Additionally, CNTPs exhibited a less negative charge (−15.8 mV) compared to CNTs (−28.5 mV) owing to the masking effect of the lipid modification, as shown in Figure 2c.…”
Section: Physicochemical Properties Of Cntps Figure 2amentioning
confidence: 94%
“…Understanding the behavior of functional groups at interfaces is of fundamental importance in physical, chemical, and biological processes such as the ions adsorption, 1-3 catalysis, [4][5][6][7] ligand recognition/binding, 8,9 and protein folding, [10][11][12] as well as the focus of various potential applications ranging from functional material fabrication, [13][14][15][16][17][18] water purification 3,19 /desalination [20][21][22][23] to drug synthesis and delivery, 24,25 biosensor. 16,26 In particular, oxygen functional groups such as epoxy, hydroxyl and carboxylic acid, covalently bond with the carbon skeleton of organic molecules and widely exist on the surface of carbon-based materials.…”
Section: Introductionmentioning
confidence: 99%