2015
DOI: 10.1016/j.colsurfa.2015.07.035
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Surface activity of amphiphilic cationic pH-responsive poly(4-vinylpyridine) microgel at air/water interface

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Cited by 20 publications
(9 citation statements)
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“…where γ o is the water surface tension (72.1 mN•m −1 ). The higher π cmc value of QAP-Br more than AIL (Table 2) indicated that the QAP-Br interacted with water via a dipole-dipole interaction mechanism more than AIL [43,44]. agree with the cmc data to confirm that the presence of asphaltene in the chemical structure of AIL increases the hydrophobic interaction of QAP-Brand increases the micelle diameter (aggregation) and their positive charges due to presence of pyridinium cations [42].…”
Section: Surface Activity Of Amphiphilic Asphaltene Pilsupporting
confidence: 70%
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“…where γ o is the water surface tension (72.1 mN•m −1 ). The higher π cmc value of QAP-Br more than AIL (Table 2) indicated that the QAP-Br interacted with water via a dipole-dipole interaction mechanism more than AIL [43,44]. agree with the cmc data to confirm that the presence of asphaltene in the chemical structure of AIL increases the hydrophobic interaction of QAP-Brand increases the micelle diameter (aggregation) and their positive charges due to presence of pyridinium cations [42].…”
Section: Surface Activity Of Amphiphilic Asphaltene Pilsupporting
confidence: 70%
“…The increasing of the Γ max value for AIL than QAP-Br (Table 2) indicates the higher adsorption of AIL at the air-water interface, which also reflects a reduction of the water surface tension. The increasing of the Γ max and lowering A min values could be explained on the basis that the interactions between the hydrophilic arms of the AIL molecules increased the packing of molecules at the interfaces [44]. The lower A min (0.033 nm 2 /molecule) of AIL suggested that its adsorption oriented away from the liquid in a more tilted position.…”
Section: Surface Activity Of Amphiphilic Asphaltene Pilmentioning
confidence: 99%
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“…The dried p(HPMA-Cl) microgel was modified using with TAEA and PEI agents [25]. A certain amount (0.5 g) of dried-p(HPMA-Cl) microgel was dispersed in 10 mL DMF, and either 6.67 mmol TAEA or 2 mL PEI was added to this mixture [26].…”
Section: The Modification Of P(hpma-cl) Microgelsmentioning
confidence: 99%
“…After 24 h, the reaction mixtures were taken into room temperature and the modified p(HPMA)-TAEA and p(HPMA)-PEI microgels were collected by centrifugation (24680 rpm, 10 min, 25ºC). The prepared microgels were washed with DMF and ethanol and dried in an oven at 50ºC [25,27]. Characterization of the microgels.…”
Section: The Modification Of P(hpma-cl) Microgelsmentioning
confidence: 99%