Surface charge at Teflon/aqueous solution of potassium chloride interfaces

被引:70
|
作者
Preocanin, Tajana [1 ]
Selmani, Atida [1 ]
Lindqvist-Reis, Patric [2 ]
Heberling, Frank [2 ]
Kallay, Nikola [1 ]
Luetzenkirchen, Johannes [2 ]
机构
[1] Univ Zagreb, Fac Sci, Dept Chem, Zagreb 10000, Croatia
[2] KIT, INE, D-76021 Karlsruhe, Germany
关键词
Hydrophobic surfaces; Teflon; Mass titration; Acid-base properties; Surface charge; Zeta potential; Contact angle; HYDROPHOBIC SURFACES; AQUEOUS-ELECTROLYTE; AIR/WATER INTERFACE; OIL/WATER INTERFACE; MASS TITRATION; DOUBLE-LAYER; WATER; IONS; HYDROXIDE; EMULSIONS;
D O I
10.1016/j.colsurfa.2012.07.025
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
The effect of potassium chloride and pH on the interfacial water layer around Teflon particles and flat Teflon surfaces was investigated. Electrokinetic measurements and potentiometric titrations were carried out as well as contact angle measurements for some selected pH values. The electrokinetic measurements at flat Teflon plates in contact with potassium chloride aqueous solution shows that the isoelectric point is at pH(iep) approximate to 3.7. The electrokinetic potential of Teflon depends on ionic strength. Potentiometric mass titrations of Teflon suspensions in different concentrations of potassium chloride show that the point of zero charge lies in the same pH region (pH(pzc) approximate to 3.5) as the pH(iep). A minimum of the contact angle was observed in the acidic region, at pH approximate to 3, close to the pH(pzc) and pH(iep). Interestingly, the calculated surface charge densities were found to be independent of the electrolyte concentration. As a possible and widely brought forward explanation it is suggested that the concentrations of OH- and H+ ions within the interfacial water layer depend on pH and are not equal. All findings together support the hypothesis that the interfacial water layer around Teflon is the origin of the interfacial charge. (C) 2012 Elsevier B.V. All rights reserved.
引用
收藏
页码:120 / 128
页数:9
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