2016
DOI: 10.3390/polym8030062
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Polydopamine Particle as a Particulate Emulsifier

Abstract: "Pickering-type" emulsions were prepared using polydopamine (PDA) particles as a particulate emulsifier and n-dodecane, methyl myristate, toluene or dichloromethane as an oil phase. All the emulsions prepared were oil-in-water type and an increase of PDA particle concentration decreased oil droplet diameter. The PDA particles adsorbed to oil-water interface can be crosslinked using poly(ethylene imine) as a crosslinker, and the PDA particle-based colloidosomes were successfully fabricated. Scanning electron mi… Show more

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Cited by 50 publications
(32 citation statements)
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“…The contact angle and zeta potential obtained for PDA agree with the values reported in the literature. 17,33 The hydrophobic surface of PEP can be attributed to the presence of additional methyl group in the precursor EP and the lower surface concentration of amine and hydroxyl groups in the resulting PEP nanostructures, which is in agreement with the zeta potentials obtained. This is further supported by the NMR data.…”
supporting
confidence: 83%
“…The contact angle and zeta potential obtained for PDA agree with the values reported in the literature. 17,33 The hydrophobic surface of PEP can be attributed to the presence of additional methyl group in the precursor EP and the lower surface concentration of amine and hydroxyl groups in the resulting PEP nanostructures, which is in agreement with the zeta potentials obtained. This is further supported by the NMR data.…”
supporting
confidence: 83%
“…In the case of pure PDA, the peaks at 1515 and 1605 cm −1 conform to the indole or indoline structures and vibration of NH . The wide peak at a range of about 3200–3500 cm −1 relates to the hydroxyls and amines structures . The phenolic OH vibration observes peaks at 1345 and 1285 cm −1 , respectively…”
Section: Resultsmentioning
confidence: 92%
“…The two bands that appeared at 1384 cm −1 and 1110 cm −1 belonged to the characteristic peaks of C-O-H and C-O on the phenolic hydroxyl. In comparison with DA, the characteristic peaks of indole and indoline structure were observed in the spectral line of PDAMS, PDAMC, AVM/PDAMS, and AVM@PDAMC, which confirmed the formation of polydopamine [34,35]. Compared with AVM, the characteristic peaks located at 2970 cm −1 , 1457 cm −1 , 1380 cm −1 , 789 cm −1 , and 595 cm −1 belonged to C-H, and the heteroaromatic ring of AVM was observed in the spectral lines of AVM/PDAMS and AVM@PDAMC.…”
mentioning
confidence: 72%