Long-range attractive forces and energy barriers in de-inking flotation: AFM studies of interactions between polyethylene and toner
The interfacial forces between a polyethylene particle and a toner substrate in alkaline aqueous solutions were studied using an atomic force microscope colloidal probe technique. Measurements were taken at pH 9 in water and solutions of 5 × 10 -4 M CaCl 2 , 1 × 10 -4 M Na oleate, and 1 × 10 -4 M Na...
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Published in | Journal of adhesion science and technology Vol. 14; no. 14; pp. 1829 - 1843 |
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Main Authors | , , , , |
Format | Journal Article |
Language | English |
Published |
Taylor & Francis Group
01.01.2000
|
Subjects | |
Online Access | Get full text |
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Summary: | The interfacial forces between a polyethylene particle and a toner substrate in alkaline aqueous solutions were studied using an atomic force microscope colloidal probe technique. Measurements were taken
at pH 9 in water and solutions of 5 × 10
-4
M CaCl
2
, 1 × 10
-4
M Na oleate, and 1 × 10
-4
M Na oleate plus 5 × 10
-4
M CaCl
2
in order to mimic the conditions present during de-inking flotation. A polyethylene particle was used to represent the air bubble. The observed interaction forces were described by the extended DLVO theory.
An energetic barrier caused by electrical double-layer repulsion was observed in water and Na oleate solutions but was greatly diminished in CaCl
2
solution. A long-range attractive force was
found to be present in these systems and was described using a simple exponential function. The long-range attractive force was virtually the same in water and CaCl
2
solution but decreased significantly
in Na oleate solution because of the reduced hydrophobicity of the interacting surfaces caused by the adsorbed carboxylate layer. However, in the presence of oleate and calcium ions the observed attraction
was even stronger and of longer range than in water and CaCl
2
solutions. Moreover, no energetic barrier was observed. These results can be attributed to the presence of precipitated calcium oleates
on the interacting surfaces. |
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ISSN: | 0169-4243 1568-5616 |
DOI: | 10.1163/156856100743266 |