2016
DOI: 10.14579/membrane_journal.2016.26.1.26
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Preparation and Characterization of Porous Polycaprolactone Membrane for Tissue Engineering

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Cited by 7 publications
(11 citation statements)
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“…For pure SPAE membrane, the membranes with higher DS had more weight loss in this step because of more content of sulfonic acid. For the blend membranes, this step mass loss was decomposition of sulfonic acid group in both SPAE and Nafion . At last, distinct step of thermal degradation, starting at about 450 °C, was assigned to the thermal degradation of polymer backbone …”
Section: Resultsmentioning
confidence: 99%
“…For pure SPAE membrane, the membranes with higher DS had more weight loss in this step because of more content of sulfonic acid. For the blend membranes, this step mass loss was decomposition of sulfonic acid group in both SPAE and Nafion . At last, distinct step of thermal degradation, starting at about 450 °C, was assigned to the thermal degradation of polymer backbone …”
Section: Resultsmentioning
confidence: 99%
“…where ῑ (A) is the average current, v (V s −1 ) is the scan rate and m (g) is the total mass of the electrode. [44,50,51]…”
Section: Characterizationmentioning
confidence: 99%
“…To reveal the interfacial bonding among various components, Fourier transform infrared spectroscopy (FTIR) spectra were studied, as shown in Figure 2e. Compared with pure MXene, TA@MXene nanosheets present not only the absorption peaks of TA (755 cm −1 corresponding to C=C in benzene rings) but also the redshift of the peak for the in-plane bending mode of surficial -OH (from 3441 cm −1 of MXene to 3418 cm −1 ), [31,32] demonstrating the formation of hydrophilic products in the modification process via the strong hydrogen bonding between TA molecules and MXene nanosheets, which subsequently leads to the homogeneous gradient distribution of TA@MXene in the aqueous PU matrix rather than the hydrophobicity causing random aggregation. [33,34] Additionally, as shown in the enlarged view (Figure S6, Supporting Information) of the red marker box in Figure 2e, the TA@MXene-rich surface has a significantly wider stretching vibration area and a pronounced redshift from 4000 to 1766 cm −1 compared with other samples, revealing the abundant multiple H-bonding interactions between the catechol groups of TA molecules and the oxygen-containing functional groups of PU and MXene [35] (Figure 2g), which is highly beneficial for realizing the self-healing performance of the Janus film.…”
Section: Materials Design and Characterizationmentioning
confidence: 99%