Films of poly-L-leucine, poly-L-valine, and poly-L-isoleucine have been studied at the air-water interface by surface balance experiments. In addition, Langmuir-Blodgett (LB) films of these polypeptides deposited onto quartz and mica have been studied by circular dichroism (CD) spectroscopy and atom
Determining Surface Potential of the Bitumen-Water Interface at Nanoscale Resolution using Atomic Force Microscopy
✍ Scribed by Jaroslaw Drelich; Jun Long; Anthony Yeung
- Publisher
- John Wiley and Sons
- Year
- 2008
- Tongue
- English
- Weight
- 768 KB
- Volume
- 85
- Category
- Article
- ISSN
- 0008-4034
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✦ Synopsis
Abstract
Atomic force microscopy (AFM) was used to measure the surface forces between a silicon nitride AFM tip and a deposited layer of Athabasca bitumen; the measurements were carried out in pure water (pH 6.0–6.5) and 1 mM KCl solution (pH 9). An AFM pyramidal‐shaped tip was moved stepwise using an operator‐controlled offset (10 nm per step) and the tip‐bitumen colloidal forces were measured at each location. Surface charge densities at the bitumen‐water interface were calculated from the measured colloidal forces using a theoretical model that combined both electrostatic and van der Waals forces for a conical tip‐flat substrate system. Fitted values of the bitumen surface charge density ranged from –0.002 to –0.004 C/m^2^ in water (pH 6.0–6.5), and –0.005 to –0.022 C/m^2^ in KCl solution (pH 9); the variation of local charge density along the bitumen surface appeared random. Bitumen surface potentials were also calculated from the surface charge densities using the Graham equation; the values ranged from –90 to –130 mV in water, and –45 to –110 mV in KCl solution. This study suggests the presence of bitumen surface domains of different surface charge densities/surface potentials. The domains are estimated to have characteristic sizes of 20 to 40 nm or less.
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