2013
DOI: 10.1016/j.jcis.2013.05.033
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Influence of drying method on the surface energy of cellulose nanofibrils determined by inverse gas chromatography

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Cited by 87 publications
(84 citation statements)
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“…K A and K B values of the samples were calculated using the DG SP values of polar probes at that particular surface coverage. Consistent with the literature (Tze et al 2006;Pommet et al 2008;Peng et al 2013), the K B for both samples was consistently higher than K A , indicating that the samples possess higher concentrations of electron-donating (basic) surface functional groups than electron-withdrawing (acidic) ones. The higher specific Gibbs Free Energy of acidic probe (like acetone) indicates the domination of electron donating groups on the surface.…”
supporting
confidence: 89%
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“…K A and K B values of the samples were calculated using the DG SP values of polar probes at that particular surface coverage. Consistent with the literature (Tze et al 2006;Pommet et al 2008;Peng et al 2013), the K B for both samples was consistently higher than K A , indicating that the samples possess higher concentrations of electron-donating (basic) surface functional groups than electron-withdrawing (acidic) ones. The higher specific Gibbs Free Energy of acidic probe (like acetone) indicates the domination of electron donating groups on the surface.…”
supporting
confidence: 89%
“…Consistent with the Lindman hypothesis, both samples are amphoteric (Lindman et al 2010) (Table S1), both powders feature higher dispersive surface energies than cotton (Kondor et al 2015) and lyocell fibers (Tze et al 2006) and are comparable to TEMPO-oxidized and genuine CNF (Peng et al 2013;Gamelas et al 2015).…”
supporting
confidence: 75%
“…The visible spectra of the NFC suspensions in the transmittance mode (Fig. 1) Please, insert Table 1 Please, insert Figure 1 The dispersion component of the surface energy ( s d ) at 40 ºC of the studied nanocelluloses was in the range of 42-52 mJ m -2 and was found to increase in the following order: NFC-5p < NFC-15p < enzymatic nanocellulose ( Please, insert Table 2 The slight increase of s d from NFC-5p to NFC-15p can be related to the aforementioned increase of the fibrillation, since a more nanofibrillated material will have a larger number of hydroxyl groups, which are considered to have a major contribution to the dispersion component of the surface energy of cellulose [18,25], accessible on the surface for interaction with the IGC apolar probes. The differences in the s d values between the TEMPO-oxidised nanocelluloses and the enzymatic nanocellulose can partly be due to the different crystallinity of the nanocelullose samples.…”
Section: Resultsmentioning
confidence: 99%
“…Not many papers reported the use of IGC to analyse nanocellulose [15][16][17][18][19]. In particular, under infinite dilution conditions, the dispersion component of the surface energy was determined for cellulose nanofibers obtained by enzymatic pre-treatments [15] and cellulose nanofibers extracted from hemp fibre by acid hydrolysis [16].…”
Section: Page 4 Of 26mentioning
confidence: 99%
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