Biomedical Engineering Reference
In-Depth Information
Ta b l e 1 .
Ionic liquids used in this study
Abbreviation
Cation
Anion
emim.BF 4
1-ethyl-3-methylimidazolium
tetrafluoroborate
bmim.BF 4
1-butyl-3-methylimidazolium
tetrafluoroborate
hmim.BF 4
1-hexyl-3-methylimidazolium
tetrafluoroborate
omim.BF 4
1-octyl-3-methylimidazolium
tetrafluoroborate
dmim.BF 4
1-decyl-3-methylimidazolium
tetrafluoroborate
bmim.PF 6
1-butyl-3-methylimidazolium
hexafluorophosphate
bmim.I
1-butyl-3-methylimidazolium
iodide
bmim.TFA
1-butyl-3-methylimidazolium
trifluoroacetate
bmim.NTf 2
1-butyl-3-methylimidazolium
bis(trifluorosulfonyl)imide
-CF 3 and -CF 2 - groups and is unaffected by the oxygen from the PDD monomers.
This apparent contradiction reflects the different sampling depths achieved with
XPS and SIMS (6-8 nm and 1-2 nm, respectively [66]) as compared with contact
angle measurements (
0.5 nm [64, 67]).
B.2. Ionic Liquids
The imidazolium-based ionic liquids used in this study are listed in Table 1.
Two series of pure ionic liquids were considered: (i) constant anion (1-alkyl-3-
methylimidazolum tetrafluoroborates, Rmim.BF 4 ) and (ii) constant cation (1-butyl-
3-methylimidazolium with various anions, bmim.X). Mixtures of bmim.BF 4 and
water with various concentrations were also included. All ionic liquids were pur-
chased from Merck and purified by extraction with activated charcoal, filtering
through a 0.2 µm Teflon filter, extraction with ethyl acetate, and evacuation under
medium vacuum (0.1 mbar) for 24 h [68].
B.3. Electrode
Glass slides, coated with a 30 nm Indium Tin Oxide (ITO) layer, were obtained
from Delta Technologies (Stillwater, MN). They were cleaned with isopropanol,
dried with nitrogen, and dip-coated with Teflon AF1600 (6% AF1600 dissolved in
Fluorinert FC-75, Derbyshire, UK). The AF1600 coating was dried in air (30 min
in a laminar flow cabinet and 30 h in an oven at 100 C). The thickness of the
AF1600 was determined by capacitance and stylus (Zeiss HandySurf profilometer)
measurements. The average thickness of the insulating layer was (3 . 8
±
0 . 2) µm.
B.4. Electrowetting
The insulated electrode was immersed in a cell (Fig. 5) filled with hexadecane
(Sigma-Aldrich 99%, additionally purified by passing it through an aluminium ox-
ide column). A small droplet of ionic liquid (typical volume 10 µl) was deposited
on the electrode with an automated syringe. The droplet was then contacted with
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