1. Ion exchange chromatography

2. Definition Ion-exchange chromatography
(or ion chromatography) is a process that allows the separation of ions and polar molecules based on the charge properties of the molecules.

3. History of IE Chromatography
Ion Chromatography (IC) was introduced in 1975 by Small, Stevens, and Bauman as a new analytical method.
In 1979, Fritz et al. described an alternative separation and detection scheme for inorganic anions, in which the separator column is directly coupled to the conductivity cell.
At the end of the 1970s, ion chromatographic techniques were used to analyze organic ions for the first time.
The 1980s witnessed the development of high efficiency separator columns with particle diameters between 5 µm and 8 µm, which resulted in a significant reduction of analysis time.
Since the beginning of the 1990s column development has aimed to provide stationary phases with special selectivity.

4. Types of Ion Chromatography
1. Ion-Exchange Chromatography (HPIC)
(High Performance Ion Chromatography)
2. Ion-Exclusion Chromatography (HPICE)
(High Performance Ion Chromatography Exclusion)
3. Ion-Pair Chromatography (MPIC)
(Mobile Phase Ion Chromatography)

5. 1. Ion-Exchange Chromatography (HPIC)
(High Performance Ion Chromatography)
This separation method is based on ion-exchange processes occurring between the mobile phase and ion-exchange groups bonded to the support material.
Ion-exchange chromatography is used for the separation of both inorganic and organic anions and cations.

6. Ion-Exclusion Chromatography (HPICE)
(High Performance Ion Chromatography Exclusion)
Ion-exclusion chromatography is particularly useful for the separation of weak inorganic and organic acids from completely dissociated acids which elute as one peak within the void volume of the column. In combination with suitable detection systems, this separation method is also useful for determining amino acids, aldehydes, and alcohols.

7. Ion-Pair Chromatography (MPIC) (Mobile Phase Ion Chromatography)
The dominating separation mechanism in ion-pair chromatography is adsorption. The stationary phase consists of a neutral porous divinylbenzene .resin of low polarity and high specific surface area
Ion-pair chromatography is particularly suited for the separation of surface-active anions and cations, sulfur compounds, amines, and transition metal complexes.

9. The matrix
An ion exchanger consists of an insoluble matrix to which charged groups have been covalently bound. The charged groups are associated with mobile counter-ions. These counter-ions can be reversibly exchanged with other ions of the same charge without altering the matrix.
1-Positively charged exchangers have negatively charged counter-ions (anions) available for exchange and are called anion exchangers.
2-Negatively charged exchangers have positively charged counter-ions (cations) and are termed cation exchangers.

10. CLASSIFICATION OF ION EXCHANGERS
پلی ساکاریدی Anion exchanger دی اتیل آمینو سلولز (DEAE-cellulose)
Cation exchanger کربوکسی متیل سلولز (CM. Cellulose)
سنتتیک : وینیل بنزن، دی وینیل بنزن
An almost unlimited variety of resins with different compositions and degrees
of cross linking can be prepared. The resins consist of an elastic three-dimensional network of hydrocarbons which carry fixed ionic groups
In a cation exchanger, the matrix carries ionic groups like
− SO3−, − COO−, − PO3
and in an anion exchanger, it carries groups such as
−NH3+, >NH2 , > N+

11. Ion Exchangers

12. Ion exchangers – Functional groups
Anion exchanger
Aminoethyl (AE-)
Diethylaminoethyl (DEAE-)
Quaternary aminoethyl (QAE-)
amphoteric exchangers
snake- cage
Polyelectrolytes
Cation exchanger
Carboxymethyl cellulose (CM-cellulose)
Sulphopropyl (SP-)

13. Cation exchange chromatography
Cation exchange chromatography retains positively charged cations because the stationary phase displays a negatively charged functional group - + + - _ - + +
R-X C +M B R-X M + C + B

14. Anion exchange chromatography
Anion exchange chromatography retains anions using positively charged functional group: _ - - - + + + +
R-X A +M B R-X B + M + A

15. Important Points to Consider For Ion Exchange Chromatography
Preparation of resin
pH of buffers
Buffer selection
Elution PH
change in ionic strength

16. procedure

17. Procedure
Dr Gihan Gawish

19. Effect of pH in the separation of proteins
By adjusting the pH or the ionic concentration of the mobile phase, various protein molecules can be separated.
For example, if a protein has a net positive charge at pH 7.0, then it will bind to a column of negatively-charged beads, whereas a negatively charged protein would not.

20. Effect of pH in the separation of proteins
Proteins are charged molecules. At specific pH, it can exist in anionic (-), cationic (+) or zwitterion (no net charge) stage.
anionic
cationic
pH =pI
pH increase
*pI isoelectric point

25. Choosing your ion-exchanger: know your proteins
Stability of proteins
stable below pI value, use cation-exchanger
stable above pI value, use anion-exchanger
Molecular size of proteins
<10,000 MW, use matrix of small pore size
10, ,000 MW, use Sepharose equivalent grade

27. Detection In Ion Chromatography
1. Conductivity detection  2. Electrochemical (amperometric or coulometric) detection  3. Potentiometric detection  4. Spectroscopic detection  5. Post-column reaction detection.

28. Post column reaction
Detection by post-column reaction (PCR) involves the chemical reaction of the solutes as they elute from the column on the fly, prior to their introduction to the detector. 

29. The performance of any detector is evaluated according to the following criteria:
• Sensitivity
• Linearity
• Resolution (detector cell volume)
(• Noise (detection limit

30. Some advantage of strong ion exchangers are:
• Sample loading capacity does not decrease at high or low pH values due to loss of charge from the ion exchanger .
• A very simple mechanism of interaction exists between the ion exchanger and the solute.
• Ion exchange experiments are more controllable since the charge characteristics of the media do not change with changes in pH. This makes strong exchangers ideal for working with data derived from electrophoretic titration curves.
Ion-exchange chromatography separates proteins by charge under near physiological and non-denaturing conditions.
its widespread applicability, its high resolving power

31. Some advantage of strong ion exchangers are:
. Speed
• Sensitivity
• Selectivity
• Simultaneous detection
• Stability of the separator columns

32. Application
i) Separation of metal ions and anions
ii) Separation of organics
iii) Separation of ionized from nonionized
iv) Separation of actinide elements
v) Miscellaneous applications.

33. Enzyme
The recovery of creatine kinase in this separation was 89%.

34. isoenzyme

35. Immunoglobulins