1. Lecture I

2. 1- Chromatographic methods A. Braithwait, E.J. Smith (1995) 2- Modern thin layer chromatography (chromatographic science services vol, 52) N. Grinberg (1990) 3- Preparative chromatography technique Hostettman K., Hostettman M. And Marston A. (1986) 4- Organic structure analysis Crews P., Rodriguez J. And Jaspers M. (1998) 5-Spectroscopic identification of organic compounds 6 th ed Robert M. Silverstein, Francis X Webster (1996).

3.  Chromatography is a technique by which compounds of mixture are separated by differential migration of dissolved sample between two immiscible phases in a specified system.  Two immiscible phases: - Mobile phase is liquid or gas - Stationary phase is adsorbent or a second liquid

4. I- According to Mobile phase A- Liquid chromatography B- Supercritical fluid chromatography C- Gas chromatography II- According to stationary phase A- Gas – solid chromatograph B- Liquid – liquid chromatograph C- Gas – liquid chromatography

5. III- According mechanism of separation A- adsorption chromatography (Solid St. Phase) B- Partition chromatography (two immiscible liquids) C- Ion exchange chromatography Which is used for separation of charged molecules by using anaionic and cationic resin

6. D- Affinity chromatography in bio fluids (antigen-antibodies reaction) E- Gel filtration chromatography (steric exclusion, or molecular sieving ) The column is packed with material having controlled pore sizes and the sample is screened or filtered according to its molecular size, there is no interaction between solute and stationary phase. The large molecules rapidly washed through the column, the smaller molecules penetrate inside the pores and elute later. Large molecules small molecules

7. IV- according to the equipment and the operational procedures A- Column chromatography - The stationary phase is packed in tube and mobile phase pass through it by gravity or pressure -Column chromatography - HPLC - GC - SEC

8. B- Planar chromatography The stationary phase is solid coated onto glass, plastics foil (TLC) or supported by cellulose fibre of paper sheet (paper chromatography)

9.  Adsorbent: finely divided homogenous solid having uniform particle size and large surface area which is capable of attracting molecules to its surface.  Chromatogram : a record at the end of chromatographic separation  Development: description of the process of chr. (running of the mobile phase through the stationary phase)

10.  Analyte; components of sample mixture  Eluent: solvent used for separation in chromatographic techniques  Effluent: liquid out of the column  Elution: seeping out of the components of the mixture in pure or partially mixed form.  Resolution: the ability of any chromatographic process to separate pure compound.

11.  Retention time: time taken to elute a particular solute  Rate of flow: distance travelled by solute / distance travelled by solvent

12.  Retention volume: volume of mobile phase required to elute a particular solute  Tailing: disadvantage of chromatography and solute is eluted in several fraction  Visualization: making the colourless bands visible

13. I- Adsorption chr. I- Column chromatography All the major chr. Process are routinely carried out using column mode For classical column chr. The following items are required

14.  The adsorption power of the adsorbent depends on e.g. Washing or heating  The larger the particle size the lower is the back pressure the faster is the flow rate and more poor is the resolution (bad separation)  The average particle diameter in open column chr. Is 10-2000um

15. The Ideal adsorbent must fulfill the following requirements:  Insoluble in mobile phase.  Inert to solutes (adsorptive).  Colorless especially when work with colored mixtures.  Suitable particle size enough to give good separation and reasonable flow rate Decrease particle size increases the surface area and consequently increases separation power..

17. A- Silica gel  is the most popular adsorbent with a general formula SiO 2 (H 2 O) n  The active sites of silica gel are the hydroxyl groups attached to silicon atoms "Silanol groups".

18.  The selective adsorptivity of activated silica is attributed to the surface silanol group which form hydrogen bond solute with a particular  Water is adsorbed by silica and inactivate it so we must activate it before using by heat at 190-200° C for two hours.  Excessive heating leads to formation of non active siloxane

19. B- Alumina  It is a porous polymer of Al 2 O 3 available in various commercial varieties for both column and planar chr.  Activation by heating at 200-400° C for 12 hrs  Types of commercial alumina : 1- Neutral alumna pH 7– 7.5. 2- Acidic alumina pH 4. It is prepared by washing aluminum oxide with 2N HCl then with distilled water. 3- Basic alumina pH 10. This type is prepared by washing with NaOH then distilled water.

20. C- Magnesium silicate (Acidic adsorbent)  It helps separate acetylated sugar steroids and essential oils. D- Kieselguhr it is prepared from the siliceous skeleton remains of microscopic marine animals. E- Charcoal colour, low sample recovery, non selective adsorptivity restrict of its use to limited application

21.  It is moving solvent that percolate through the stationary phase  Ideal mobile phase - inert - low boiling point - Low toxicity - Low price - Low viscosity - Non volatile

22. 1- Column material and diameter 2- Packing of column 3- Sample loading 4- Development 5- Fractions collection

23. 1- column material, dimensions  Columns are made up of glass, stainless or synthetic polymer  Tube-like glass column with length 10-100 times the internal diameter 2- packing of the column  There are two types of packing a- wet packing (slurry) - the specified amount of adsorbent is distributed in mobile phase in a beaker - the slurry is poured into the column after closing the bottom by cotton and close the tape

25. - the solvent flow start by opening the tape (outlet) until the packing is settled.  b- dry packing - dry adsorbent is poured directly in the column - solvent pass through the adsorbent 3- sample loading (application of sample)  There are two methods of sample loading a- dry method  The sample is adsorbed onto small amount of stationary phase, dry, then delivered onto column top

27. 2- wet method  Dissolve the sample in a small volume of the mobile phase and delivered onto the top of the column. 4- column development (elution)  The process start by the continuous passage of suitable phase (mobile ph.) through the stationary phase

28.  1- Gradient elution  2- Isocratic elution

29. GRADIENT ELUTIONISOCRATIC ELUTION  The mobile phase composition is changed during the separation process.  The mobile phase composition remains constant throughout the separation procedure.

30. Advantages of gradient elution technique 1- Shortening the time of analysis. 2- Reduces tailing, gives sharp peak. 3- Increases the sensitivity of analysis. 4- Decreases the retention of the later- eluting components so that they elute faster. 5- substances with different properties can be separated in one operation.

31. A- Tailing  Is formation of diffusely bounded zone or band in the development Process. B- Fronting  Fronting is represented by extended diffused front portion of the peak and Sharpe tail.  Factors leading to tailing 1. strong interaction between solute and stationary phase 2. application of excessive amount of the sample to the column 3. poor column packing 4. improper selection of mobile phase  occurs when the interaction between solute molecules is strong relative to those between solute and stationary phase