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What is the principle of micellar electrokinetic capillary chromatography? How does it differ from CZE?

Short Answer

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The micellar electrokinetic capillary chromatography or MEKC involves the differential movement of micelles that are ionic through the buffer solution. It is different from CZE wherein the surfactant is added such that micelles are formed that form two phases and are negatively charged and move towards the cathode.

Step by step solution

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Step 1. Given information

Explain the principle of micellar electrokinetic capillary chromatography and its difference from capillary zone electrophoresis (CZE).

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Step 2. Principle of micellar electrokinetic capillary chromatography  

Micellar Electrokinetic Capillary Chromatography (MEKC) is a technique that involves the use of a surfactant that has a long chain. It could be sodium dodecyl sulfate. As this has a long hydrocarbon chain, it is identified by a hydrophobic end that has a functional group as its head. The negative charge ends group together to form micelles that move towards the cathode. Besides, in this method both the phases are mobile.

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Step 3. Capillary Zone Electrophoresis 

Capillary Zone Electrophoresis (CZE) is one of the simplest forms of capillary electrophoresis. Here the capillary tube is filled with buffer solution and the ends are placed in the solution having additional buffer solution. The end having the sample is considered as anode wherein solutes migrate towards the cathode. The order it elutes is cations first, neutral ions, and then lastly the anions.

The direction of electroosmotic flow can be reversed by adding alkyl ammonium salt wherein the alkyl ammonium ion is hydrophobic and is positively charged and binds with negatively charged silanate ions. The result is positively charged which attracts anions. Here the order of elution is opposite to the normal. CZE helps in separating charged species namely proteins, amines, etc.

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Step 4. The main difference between MECC and CZE

  1. Micelles are not present in CZE while it is present in MEKC
  2. In CZE, the ions migrate according to ionic mobility to separate into zones under influence of the electric field.
  3. In MEKC, there is the option of changing column packing to alter the stationary state, unlike CZE.
  4. In CZE, it has limitations in separating neutral species.

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Most popular questions from this chapter

In an interesting paper, Zheng and coworkers (J. Zheng, L. T. Taylor, J. D. Pinkston, and M. L. Mangels, J. Chromatogr. A, 2005, 1082, 220, DOI: 10.1016/j.chroma.2005.04.086) discuss the elution of polar and ionic compounds in SFC.

(a) Why are highly polar or ionic compounds usually not eluted in SFC?

(b) What types of mobile-phase additives have been used to improve the elution of highly polar or ionic

compounds?

(c) Why is ion-pairing SFC not often used?

(d) Why are ammonium salts sometimes added as mobile-phase modifiers in SFC?

(e) The authors describe an SFC system that uses mass spectrometry (MS) as a detector. Discuss the

interfacing of an SFC unit to a mass spectrometer. Compare the compatibility of SFC with MS to that

of HPLC and GC with MS.

(f) The authors studied the effect of column outlet pressure on the elution of sodium 4-dodecylbenzene

sulfonate on three different stationary phases with five mobile-phase additives. What effect was

observed, and what was the explanation for the effect?

(g) What elution mechanisms were considered by the authors?

(h) Which mobile-phase additive gave the fastest elution of the sulfonate salts? Which provided the

longest retention times?

(i) Did a silica column give results similar to or different from a cyano bonded-phase column?

Three large proteins are ionized at the pH at which an electrical FFF separation is carried out. If the ions are designated A2+,B+,and C3+, predict the order of elution.

Suggest how electroosmotic flow might be suppressed.

Why does pH affect the separation of amino acids by electrophoresis?

What is electroosmotic flow? Why does it occur?

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