Title: Advanced Analytical Chemistry
1Advanced Analytical Chemistry CHM 6157 Y.
CAI Florida International UniversityUpdated on
10/17/2006 Chapter 9 Capillary Electrophoresis
- Chapter 9 Capillary Electrophoresis (CE)
- References
- Dale R. Baker, Capillary Electrophoresis, John
Wiley Sons, 1995. - M.G. Khaledi, Ed., High-Performance Capillary
Electrophoresis, John Wiley Sons, 1998.
2Advanced Analytical Chemistry CHM 6157 Y.
CAI Florida International UniversityUpdated on
10/17/2006 Chapter 9 Capillary Electrophoresis
1. An Overview of capillary electrophoresis
3Advanced Analytical Chemistry CHM 6157 Y.
CAI Florida International UniversityUpdated on
10/21/2008 Chapter 9 Capillary Electrophoresis
- Column offers
- Ease of quantitation
- Automation
- Fraction collection
- On-line coupling to structure specific detectors,
including MS, NMR - Jorgenson and Lukacs (Anal. Chem., 1981, 53,
1298) were the first to produce an operational
capillary electrophoresis unit and demonstrate
its high resolving power.
4Advanced Analytical Chemistry CHM 6157 Y.
CAI Florida International UniversityUpdated on
10/17/2006 Chapter 9 Capillary Electrophoresis
5Advanced Analytical Chemistry CHM 6157 Y.
CAI Florida International UniversityUpdated on
10/17/2006 Chapter 9 Capillary Electrophoresis
- 1.1 Some concepts
- Electrophoresis is the movement of electrically
charged particles or molecules in a conductive
liquid medium, usually aqueous, under the
influence of an electric field.
6Advanced Analytical Chemistry CHM 6157 Y.
CAI Florida International UniversityUpdated on
10/17/2006 Chapter 9 Capillary Electrophoresis
7Advanced Analytical Chemistry CHM 6157 Y.
CAI Florida International UniversityUpdated on
10/17/2006 Chapter 9 Capillary Electrophoresis
- Electroosmotic flow Under the influence of an
electric field, the buffer and the neutral
molecules also move through the tube, due to
Electroosmotic flow (well discuss the
Electroosmotic flow in more details later).
8Advanced Analytical Chemistry CHM 6157 Y.
CAI Florida International UniversityUpdated on
10/17/2006 Chapter 9 Capillary Electrophoresis
9Advanced Analytical Chemistry CHM 6157 Y.
CAI Florida International UniversityUpdated on
10/17/2006 Chapter 9 Capillary Electrophoresis
- Zone Spreading
- Theoretically, in electrophoresis, the compounds
will travel through the conductive medium as zone
that do not diffusion or spread out in the
absence of any other influences except for the
electric field.
10Advanced Analytical Chemistry CHM 6157 Y.
CAI Florida International UniversityUpdated on
10/17/2006 Chapter 9 Capillary Electrophoresis
- Zone electrophoresis refers to the migration of
molecules as zones which do not undergo zone
spreading due to diffusion. - Longitudinal and radical diffusion
- Do not contribute much zone spreading
- Molecular diffusion rate in a liquid is
relatively small compared to the rate at which
they migrate through the liquid
11Advanced Analytical Chemistry CHM 6157 Y.
CAI Florida International UniversityUpdated on
10/17/2006 Chapter 9 Capillary Electrophoresis
- Thermal or convective diffusion
- Contributes significantly to zone spreading
- Electric current causes Joule heating
- Molecules in the warmer, center of a tube migrate
faster than those near the cooler wall, leading
to zone spreading - Minimize the amount of heat generated and
dissipate that heat. - In addition to causing zone spreading, high T may
also cause thermal degradation of some molecules
12Advanced Analytical Chemistry CHM 6157 Y.
CAI Florida International UniversityUpdated on
10/17/2006 Chapter 9 Capillary Electrophoresis
Influence of tube diameter on convective
diffusion In a round tube, the temperature
difference between the center and the wall of the
tube, ?T, can be calculated from ?T
(0.239Q/4k)r2 1 where Q is the power
density in watts/m3, k is thermal conductivity
of the solution, and r is tube radius.
13Advanced Analytical Chemistry CHM 6157 Y.
CAI Florida International UniversityUpdated on
10/21/2008 Chapter 9 Capillary Electrophoresis
- Minimize convective diffusion decrease diameter
of the capillary - Less current is generated for a given voltage,
and less joule heat is produced. - Fast dissipation of the heat (increase in the
inner surface area-to-volume ratio of the tube). - Therefore
- Narrow capillary has been selected 50 -75 ?M
i.d. - 400,000 theoretical plates with 80-100 cm long
(20,000 by HPLC) -
14CE is referred to
Advanced Analytical Chemistry CHM 6157 Y.
CAI Florida International UniversityUpdated on
10/21/2008 Chapter 9 Capillary Electrophoresis
- Capillary electrophoresis is sometimes referred
to as Capillary zone Electrophoresis (CZE), - Free solution Capillary Electrophoresis (FSCE)
- High-performance Capillary Electrophoresis (HPCE)
- Capillary Electrophoresis (CE).
15Advanced Analytical Chemistry CHM 6157 Y.
CAI Florida International UniversityUpdated on
10/17/2006 Chapter 9 Capillary Electrophoresis
1.2 CE system overview
16Advanced Analytical Chemistry CHM 6157 Y.
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17Advanced Analytical Chemistry CHM 6157 Y.
CAI Florida International UniversityUpdated on
10/17/2006 Chapter 9 Capillary Electrophoresis
CE Electropherograms and HPLC chromatograms Assum
ing equal solute concentrations and detector
responses
18Advanced Analytical Chemistry CHM 6157 Y.
CAI Florida International UniversityUpdated on
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- HPLC chromatograms
-
- In isocratic HPLC, the longer the retention time,
the broader and the shorter the peaks. This is
because solutes are diluted more as they spend
more time inside the column. - Area of all the peaks are approximately the same
since all solutes through the detector at the
same rate.
19Advanced Analytical Chemistry CHM 6157 Y.
CAI Florida International UniversityUpdated on
10/17/2006 Chapter 9 Capillary Electrophoresis
- CE Electropherograms
- Peak height remain constant as retention gets
longer because the solutes move through the
detector in zones of approximately the same
length and, therefore, the same concentration. - The peak get wider with time because the later
eluting solutes move through the detector more
slowly, and consequently, reside in the detector
cell longer. For equal concentrations and
detector responses, the peak areas increase with
time.
20Advanced Analytical Chemistry CHM 6157 Y.
CAI Florida International UniversityUpdated on
10/17/2006 Chapter 9 Capillary Electrophoresis
- Sample injection
- Hydrodynamic by pressure or siphoning
(gravity). - Electrokinetic an electric field is applied to
the sample vial, causing the sample components to
migrate into the capillary.
21Advanced Analytical Chemistry CHM 6157 Y.
CAI Florida International UniversityUpdated on
10/21/2008 Chapter 9 Capillary Electrophoresis
Capillaries Fused silica capillaries (30-100 cm
long with inner diameters of 50-75 ?m and outer
diameters of 375 ?m). Detectors UV/Vis,
Fluorescence, conductivity, MS, ICP/MS, NMR
(new)...... Power supply Voltages up to 30 kV,
currents up to 300 ?A, and power up to 6 W.
22Advanced Analytical Chemistry CHM 6157 Y.
CAI Florida International UniversityUpdated on
10/17/2006 Chapter 9 Capillary Electrophoresis
- 1.3 Comparison of CE to other separation
techniques - Efficiency
- Efficiency, N, expressed as the number of the
theoretical plates, is related to how narrow the
peaks are in a chromatogram or electropherogram. - N 16(t/w)2
- The narrower the peak, the higher the
efficiency, and the better the separation. - CE has very high efficiency compared to HPLC and
GC.
23Advanced Analytical Chemistry CHM 6157 Y.
CAI Florida International UniversityUpdated on
10/17/2006 Chapter 9 Capillary Electrophoresis
- Sample type
- HPLC and GC are complementary.
- HPLC and CE are more competitive with each
other. - CE can use buffers that covers a wide pH range,
whereas most silica-based HPLC column cannot be
used with mobile phases at pH above about eight. - Sample volume
- CE the relatively small volume (few nl) of
sample. A capillary that is 50 cm long and 50 ?m
i.d. has a volume of only 0.98 ?l.
24Advanced Analytical Chemistry CHM 6157 Y.
CAI Florida International UniversityUpdated on
10/17/2006 Chapter 9 Capillary Electrophoresis
- Detection limit
- The Concentration detection limit of CE is not
as good as HPLC and GC, roughly 100-1000 times
higher. - Confused about
- Concentration detection limit
- Instrument detection limit
- Sensitivity
- Reagent requirements
- Compared to HPLC, CE requires much less amount
solvents, typically a few ml for a day of
analysis.
25Advanced Analytical Chemistry CHM 6157 Y.
CAI Florida International UniversityUpdated on
10/17/2006 Chapter 9 Capillary Electrophoresis
- Principles
- 2.1 Electroosmotic flow (EOF)
- In CE, in addition to the solutes, the buffer
solution usually also moves through the capillary
under the influence of an electric field. This
phenomenon is termed electroosmotic flow. In
normal operation, the direction of EOF is toward
the negatively charged cathode. - 2.1.1 Benefits of EOF
- Separate anions and cations in a single run.
- Neutral solutes would not move through the
capillary tube. - Reduces the analytical time
26Advanced Analytical Chemistry CHM 6157 Y.
CAI Florida International UniversityUpdated on
10/17/2006 Chapter 9 Capillary Electrophoresis
27Advanced Analytical Chemistry CHM 6157 Y.
CAI Florida International UniversityUpdated on
10/23/2008 Chapter 9 Capillary Electrophoresis
2.1.2 Formation of EOF
Silanol groups have strong affinity for polar
organic molecules.
Can be deactivated by silanization with
dimethylchlorosilane (DMCS).
28Advanced Analytical Chemistry CHM 6157 Y.
CAI Florida International UniversityUpdated on
10/17/2006 Chapter 9 Capillary Electrophoresis
solvated
29Advanced Analytical Chemistry CHM 6157 Y.
CAI Florida International UniversityUpdated on
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solvated
The build up of ions at the capillary wall (image
courtesy of Agilent Technologies)
http//www.chemsoc.org/ExemplarChem/entries/2003/l
eeds_chromatography/chromatography/eof.htm
30Advanced Analytical Chemistry CHM 6157 Y.
CAI Florida International UniversityUpdated on
10/17/2006 Chapter 9 Capillary Electrophoresis
- Silanol (Si-OH) groups are ionized to negatively
charged silanoate (Si-O-) groups at pH above
about three. This ionization can be enhanced
first by passing a basic (KOH or NaOH) solution
through the capillary followed by the buffer. - The negatively charged silanoate groups then
attract positively charged cations from the
buffer, which form an inner layer of cations at
the capillary wall. These cations are not of
sufficient density to neutralize all the negative
charges, so a second, outer layer of cations
forms. The inner layer is tightly held by the
Si-O- groups and is referred to as the fixed
layer. The outer layer of cations is not tightly
held because is it further away from the
silanoate groups, and it is referred to as mobile
layer. These two layers make up the diffuse
double layer of cations. - When an electric field is applied, the mobile,
outer layer of cations is pulled toward the
negatively charged cathode. Since these cations
are solvated, they drag the bulk buffer solution
with them, thus causing EOF.
31Advanced Analytical Chemistry CHM 6157 Y.
CAI Florida International UniversityUpdated on
10/17/2006 Chapter 9 Capillary Electrophoresis
Zeta potential (?) is an electrical imbalance
created at the plane of shear, which is the
potential difference across the layers. ?
4??e/? where ? is the thickness of the diffuse
double layer, e is the charge per unit surface
area, ? is the dielectric constant of the
buffer. EOF is proportional to the zeta
potential.
32Advanced Analytical Chemistry CHM 6157 Y.
CAI Florida International UniversityUpdated on
10/17/2006 Chapter 9 Capillary Electrophoresis
2.1.3 EOF Velocity and Mobility The velocity,
vEOF, vEOF ? ? E/4?? where E is the
applied electric field in volts/cm, and ? is the
viscosity of the buffer. The mobility, ?EOF,
?EOF ? ? /4?? Note that ?EOF is dependent
solely on buffer characteristics, and independent
of the applied electric field.
33Advanced Analytical Chemistry CHM 6157 Y.
CAI Florida International UniversityUpdated on
10/17/2006 Chapter 9 Capillary Electrophoresis
- Significant parameters that affect EOF
- Applied Voltage
- Migration time
- Currents and Joule heating
- Zone spreading.
34Advanced Analytical Chemistry CHM 6157 Y.
CAI Florida International UniversityUpdated on
10/23/2008 Chapter 9 Capillary Electrophoresis
Excessive heat produced Resistance goes
down Causing increase in current
Question? Effects of capillary length and
diameter on maximum voltage selection
35Advanced Analytical Chemistry CHM 6157 Y.
CAI Florida International UniversityUpdated on
10/17/2006 Chapter 9 Capillary Electrophoresis
- (2) Buffer pH
- Changes zeta potential. As pH increases, EOF
increases, primarily because at higher pH, there
more dissociation of Si-OH to Si-O- on the inner
surface of the capillary. - Influence the degree of ionization of the solutes
and hence their mobility. - Must consider the effect on separation
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37Advanced Analytical Chemistry CHM 6157 Y.
CAI Florida International UniversityUpdated on
10/23/2008 Chapter 9 Capillary Electrophoresis
(3) Buffer concentration Effect on zeta
potential
Question? Why cannot the buffer concentration be
too low?
38Advanced Analytical Chemistry CHM 6157 Y.
CAI Florida International UniversityUpdated on
10/23/2008 Chapter 9 Capillary Electrophoresis
- (4) Temperature
- Effect on viscosity of the buffer. A temperature
increase of 1 ?C, from 20 to 21?C, reduces the
viscosity of water by 2.4. - ? 4??e/?
- ?EOF ? ? /4??
- Temperature has effect on ?, but cancelled (see
above equations). - Zone spreading
- Compound decomposition
39Advanced Analytical Chemistry CHM 6157 Y.
CAI Florida International UniversityUpdated on
10/17/2006 Chapter 9 Capillary Electrophoresis
- 2.1.4 Measurement of EOF
- Neutral marker
- Requirement of neutral markers
- Uncharged under the pH of the buffer
- Detectable by detector
- No interaction with the capillary and the buffer.
40Advanced Analytical Chemistry CHM 6157 Y.
CAI Florida International UniversityUpdated on
10/17/2006 Chapter 9 Capillary Electrophoresis
- Current monitoring
- The capillary and destination vials are filled
with buffer, and the source vial filled with the
same buffer, but at a slightly different
concentration.
41Advanced Analytical Chemistry CHM 6157 Y.
CAI Florida International UniversityUpdated on
10/17/2006 Chapter 9 Capillary Electrophoresis
2.1.5 Reverse EOF
Normal CE
Reverse EOF
42Advanced Analytical Chemistry CHM 6157 Y.
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Detector
a
c
Eletrophoretic mobility of formate ion 5.7 x
10-4 cm2/V EOF 4.2 x 10-4 cm2/V
43Advanced Analytical Chemistry CHM 6157 Y.
CAI Florida International UniversityUpdated on
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Why and How
44Advanced Analytical Chemistry CHM 6157 Y.
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2.2 Electrophoretic mobility Electrophoretic
velocity, ?EP, in cm/s ?EP
?EPE 1 ?EP eletrophoretic
mobility E applied electric field.
45Advanced Analytical Chemistry CHM 6157 Y.
CAI Florida International UniversityUpdated on
10/17/2006 Chapter 9 Capillary Electrophoresis
- Electrophoretic mobility ?EP
- ?EP q/6??r 2
- q the charge of the ionized solute
- ? buffer viscosity
- r solute radius
- ?EP is dependent on both mobility and electric
field. - ?EP is dependent only on solute and buffer
properties - Neutral molecules ?EP 0
46Advanced Analytical Chemistry CHM 6157 Y.
CAI Florida International UniversityUpdated on
10/17/2006 Chapter 9 Capillary Electrophoresis
A solutes velocity is influenced both by its
velocity of EOF, vEOF and ?EP. The observed
electrophoretic velocity, vOBS vOBS vEOF
vEP 3 In normal CE, that is the detector
is on the negatively charged side, and EOF is
from source to detector. Anions vOBS lt vEOF
Cations vOBS gt vEOF Neutals vOBS vEOF
47Advanced Analytical Chemistry CHM 6157 Y.
CAI Florida International UniversityUpdated on
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- The observed electrophoretic mobility, ?OBS
- ?OBS ?EOF ?EP 4
48Advanced Analytical Chemistry CHM 6157 Y.
CAI Florida International UniversityUpdated on
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2.2.1 Measure electrophoretic velocity and
mobility vOBS l/tm 5 tm migration
time l the effective length of capillary, from
inlet to detector. The electroosmotic velocity,
vEOF, can be determined by measuring the
migration time of a neutral marker, tnm. Then
vEP l/tm - l/tnm 6
49Advanced Analytical Chemistry CHM 6157 Y.
CAI Florida International UniversityUpdated on
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Electrophoretic mobility EV/L V is the
voltage L is the total length vEP ?EPE ?EP
vEPL/V 7 ?EP (l/tm- l/tnm)(L/V) 8
50Advanced Analytical Chemistry CHM 6157 Y.
CAI Florida International UniversityUpdated on
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2.2.2 Parameters influencing ?EP ?EP
q/6??r Solute charge Solute size Buffer
viscosity
51Advanced Analytical Chemistry CHM 6157 Y.
CAI Florida International UniversityUpdated on
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2.3 Effects of electrophoretic parameters on
separation
Chromatographic Parameters
52Advanced Analytical Chemistry CHM 6157 Y.
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53Advanced Analytical Chemistry CHM 6157 Y.
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- 2.3.1 Migration Time (tm)
- tm l/ vOBS 9
- l effective capillary length
- vOBS ?OBSE 10
- tm l/(?OBSE) 11
- tm lL/(?OBSV) 12
- tm lL/(?EP ?EOF)V 13
54Advanced Analytical Chemistry CHM 6157 Y.
CAI Florida International UniversityUpdated on
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Definition of plate height in Chromatography
55Advanced Analytical Chemistry CHM 6157 Y.
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The area of triangle is 96 of total area under
the peak. ( 2 ?) W 4?
H ?2/L 14
56Advanced Analytical Chemistry CHM 6157 Y.
CAI Florida International UniversityUpdated on
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Since W 4?
16
17
Because H ?2/L, H L/N, N L2/?2 18
57Advanced Analytical Chemistry CHM 6157 Y.
CAI Florida International UniversityUpdated on
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N 16(tR/w)2 19 Or N
5.54(tR/w1/2)2 20 Same for CE N
16(tm/w)2 21 Or N 5.54(tm/w1/2)2 22 E
fficiency, N, is expressed as the number of
theoretical plates. w peak width measured at
the base of the peak w1/2 peak width measured
at the half the peak height
58Advanced Analytical Chemistry CHM 6157 Y.
CAI Florida International UniversityUpdated on
10/17/2006 Chapter 9 Capillary Electrophoresis
The amount that a zone spreads is given by its
spatial variance, ?2, which is how much an
infinitely thin zone will diffuse over time,
t ?2 2Dt 23 D the solutes diffusion
coefficient in cm2/s.
59Advanced Analytical Chemistry CHM 6157 Y.
CAI Florida International UniversityUpdated on
10/17/2006 Chapter 9 Capillary Electrophoresis
- Assuming that all adsorption of sample, and no
radial diffusion, Substituting Eq 13 for t in
23 - tm lL/(?EP ?EOF)V 13
- ?2 2DlL/(?EP ?EOF)V 24
- Because N L2/?2
- Substituting Eq 24 for ?2
- N (?EP ?EOF)V/2D 25
60Advanced Analytical Chemistry CHM 6157 Y.
CAI Florida International UniversityUpdated on
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2.3.3 Selectivity (relative migration rates) In
HPLC, selectivity, ?, is given by ?
(t2-to)/(t1-to) A similar expression as that used
in Chromatography can be used for in CE. ?
(t2-tnm)/(t1-tnm) 26 where t2 and t1 are
migration times of adjacent peaks, and tnm is the
migration of a neutral marker.
61Advanced Analytical Chemistry CHM 6157 Y.
CAI Florida International UniversityUpdated on
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2.3.4 Resolution The most important separation
parameter is resolution, that is, how well the
components in a mixture are separated.
Resolution, R, can be calculated from an
electropherogram using R ?t/wAVE R
2(t2-t1)/(w1w2) 27 where w1 and w2 are peak
widths of adjacent peaks.
62Advanced Analytical Chemistry CHM 6157 Y.
CAI Florida International UniversityUpdated on
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Recall in chromatography, we assume WA WB
W R (tR)B (tR)A/W N 16(tR/W)2
63Advanced Analytical Chemistry CHM 6157 Y.
CAI Florida International UniversityUpdated on
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- In CE?
- James W. Jorgenson et al. Anal. Chem. 1981, 53,
1298-1302. - James W. Jorgenson et al., Science, 1983,
222,266-272. - J.C. Giddings, Separation Sci. 1969, 4, 181.
64Advanced Analytical Chemistry CHM 6157 Y.
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