Indian Institute of Chromatography and Mass Spectrometry Keep learning
Transcription
Indian Institute of Chromatography and Mass Spectrometry Keep learning
Indian Institute of Chromatography and Mass Spectrometry No.7, Chakrapani road, Guindy, Chennai 600 032, Tamil Nadu, India Keep learning IICMS NEWSLETTER Introduction to Ion-Exchange Chromatography S IICMS-NL-12-006 MAR ‘2012 IICMS at a glance ‘Chromatography’ is the general term for a variety of physico-chemical separation techniques, in which the common property is that the distribution of analyte component between the mobile phase and stationary phase. Based on these distribution properties and the physical state of mobile phase and stationary phase, the chromatographic techniques are subdivided into various classes. In these subdivided classes, if the component separation is based on ion-exchange processes, i.e., occurring between the mobile phase and the Ion-exchange groups bonded to the stationary phase called “Ionexchange chromatography”. Ion-exchange chromatography is used for the separation of both inorganic anions and cations. This newsletter focuses on the historical perspective of ion-exchange chromatography and its mechanism of separations. History: Ion exchange has been known from the time of Aristotle (330 BC), who has mentioned that sand filters were used for the purification of sea water and impure drinking waters.(1) In 1623, Francis Bacon and Hales described a method for removing salts by filtration and desalination from sea water(2). In 1790, Lowritz purified sugar beet juice by passing through charcoal(2) . Considering these works, the practical applications of ion exchange were well recognized before the 19th century, but the physical phenomenon was not known at that time. The identification of ion exchange phenomenon was attributed by two agricultural chemists, Thomson and Way. In 1850, they reported the first systematic observation on ion exchange with soils. The soil had a greater ability to absorb ammonia from fertilizers. They passed a fertilizer solution containing ammonia through the column filled with soil. The ammonium ions were taken up by the soil and an equivalent amount of calcium and magnesium ions were released. They have concluded that the soils could retain cations such as NH4+, K+ and Na+ ions and equivalent amounts of Ca2+ and Mg + ions were released.(3) Earth Ca2+ + 2NH4+ Earth 2NH4+ +Ca2+ In 1850, Eichorn recognized the alumino silicates (zeolites) are responsible for the ion exchange process in soil. The first synthetic aluminum based industrial ion exchanger was prepared in 1903 by Harm and Rumpler to purify the beet syrup. In 1905, Gans succeeded in utilizing the synthetic aluminum silicates ion exchangers for industrial purpose like water softening and sugar solution treating. But it could not success in industries because it’s poor reproducibility and chemical stability(2). The real breakthrough in this field eclipsed in 1936, Adams and Holmes synthesized insoluble organic ion exchangers by condensing the formaldehyde with polyhydric phenols / phenolsulphonic acids yield cation exchangers and anion exchangers were prepared by condensation with amines. They synthesized several organic ion exchangers, which had better properties (4). IICMS Newsletter IICMS-NL-12-006 Page 1 of 4 The ion exchange separation technique played a major role in the identification of trans-uranium elements during the Second World War. This technique was required to separate and concentrate the radioactive elements needed to create atom bomb. The next success of ion exchange chromatography was the separation of rare earth elements and separates the trace level impurities. In 1971, Dow chemical company was started the research with Small, Stevens and Baumann. They described a novel ion- exchange chromatography method for the separation and conductometric detection of anionic and cationic molecules. In the mean time, the term “Ion chromatography” has been coined by Dionex Corporation for this ionexchange chromatographic technique on 1975 (5). Further, Ion chromatography has been categorized into three major types based on their separation mechanism. They are: 1) Ion exclusion chromatography (IC) 2) Ion pair chromatography (IPC) 3) Ion exchange chromatography (IEC) Ion exclusion chromatography (IC) Ion exclusion chromatography is a useful technique for the separation of ionic and non-ionic substances using an ion exchange stationary phase in which ionic substances are rejected by the resin while non-ionic or partially ionized substances are retained and separated by partition between the liquid inside the resin particles and the liquid outside of the resin particles. The ionic substances are transitory quickly through the column but non-ionic or partially ionized substances are eluted more slowly(6). Fig-1 Schematic diagram of ion exclusion chromatography (7) • The mechanism of Ion exclusion chromatography proposes the sulfonate groups are fixed on the surface of the resin and form a negatively charged shield on the polymeric surface; often refer to as ‘Donnan membrane’. • The interior of the resin contains some occluded component, which is act as a stationary phase. • The Donnan membrane separates moving fraction of eluent (mobile phase) from occluded component of the stationary phase. • The analyte molecules enter the column; they interact with the sulfonated groups. The dissociated fraction (HCl) of the analyte is repelled from the vicinity of the Donnan membrane, while the non-dissociated molecule (R-COOH) penetrates the membrane and enters the occluded fraction of the eluent and thus effects the analyte separation. IICMS Newsletter IICMS-NL-12-006 Page 2 of 4 Ion pair chromatography (IPC) Ion pair chromatography (IPC) is a modification of reverse phase chromatography for the separation of ionic samples. The only difference in conditions of IPC is the addition of an ion pairing reagent (R+ or R-) to the mobile phase, which can interact with ionized acids (A-) or bases (BH+) to achieve the separation. Most commonly used ion-pair reagents are alkylsulfonates (R–SO3-), tetraalkylammonium salts (R4N+) and strong carboxylic acids like Trifluoroacetic acid (TFA), Heptafluorobutyric acid (HFBA), etc.,(8) (Acids) Ionized solute A- + R+ Ion pair A-R+ (Bases) BH+ + R- BH+R- Fig-2 Schematic diagram of ion-pair chromatography (7) Ion pair chromatography mechanism is completely different from Ion exclusion chromatography. Highly nonpolar stationary phases are used in reversed phase chromatography. The anionic or cationic surfactants containing ion pair reagent (lipophilic counter ion) is added to the eluent (mobile phase), which is responsible for regulating the retention of ionic compounds. The opppositively charged analyte ion and ion pair reagent together with form non polar molecule. Molecules can be retarded at the stationary phase by hydrophobic interaction. These induced interaction leads to the retention of analyte. Ion exchange chromatography (IEC) Ion exchange chromatography technique separates the ionic molecules based on their charge properties. Ion exchange occurs between the analyte ions and counter ions (ions in the mobile phase) interaction with the stationary phase ionic groups of opposite charge. The strength of interaction depends upon the charge of molecules and the stationary phase (resin) due to the difference in their charges, charge density and distribution charge on their surfaces. The interaction can be controlled by adjusting the ionic strength and pH of the mobile phase(9). The stationary phase used in Ion exchange chromatography are displays the functional groups having positive (+ve) or negative (-ve) charge properties and are termed as anion and cation respectively. 1) Anion exchanger - The analyte ions interact with the basic ion exchanger sites of the stationary phase. 2) Cation exchanger - The analyte ions interact with the acidic ion exchanger sites of the stationary phase. Steps involved in the mechanism of ion exchange chromatography: 1) Equilibration 2) Adsorption 3) Desorption 4) Regeneration IICMS Newsletter IICMS-NL-12-006 Page 3 of 4 Equilibration Adsorption Desorption End of desorption Regeneration Fig-3 Schematic diagram of ion exchange chromatography(10) • Prior to the sample injection, column must be equilibrated with the mobile phase (eluent). The equilibration of the stationary phase depends on the pH and ionic strength of mobile phase. The stationary phase charged groups are associated with mobile phase counter ions called Equilibration. Most commonly used counter ions are chloride and sodium. • The ionic strength of the analyte must be equal to the mobile phase ionic strength, to get the good analyte separation. If the ionic strength of mobile phase is too low than analyte, it allows the analyte to strongly bind with stationary phase and retains the analyte molecule called Adsorption. If the ionic strength of the mobile phase is too high than analyte, it does not allow the analyte to bind with stationary phase and the analyte molecule quickly pass through the column called Desorption. • After the molecules are eluted, the column is regenerated by high concentration of counter ions. High concentration of counter ions, removes the fouling material adsorbed to the stationary phase called Regeneration. After regeneration, the stationary phase can be equilibrated with the mobile phase for the next analysis. To summarize, Now we know, the mechanism behind the separation of 1) Ion exclusion chromatography (IC) 2) Ion pair chromatography (IPC) 3) Ion exchange chromatography (IEC) References: 1. 2. Vassilis J. Inglezakis (2006) Adsorption, ion exchange and catalysis, first edition, Elsevier inc; chapter 2, Page 38. Mu.Naushad, Ion exchange letters; Inorganic and composite ion exchange materials and their applications; 2009, page 1-14. 3. Yeshajahu Pomeranz, Clifton E. Meloan (1994), Food Analysis: Theory and Practice: Third edition; Aspen publication; chapter 20; page 313-317. 4. Zdeněk Deyl, Karel Macek; (1975) Liquid column chromatography: a survey of modern techniques and applications; Journal of chromatography library -volume 3; Elsevier inc ;chapter 9; Page 205. 5. Paul R. Haddad, Peter E. Jackson (1990); Ion chromatography: principles and applications; Journal of chromatography library - volume 46; Elsevier inc; chapter 1; page 6-7 6. Lokesh Bhattacharyya, Jeffrey S. Rohrer; Application of Ion chromatography in the analysis of pharmaceutical and biological products; Wiley publication; chapter 2. 7. Maximilian Kolb, Andreas Seubert; practical ion chromatography-An introduction; Metrohm publication; page 19-20. 8. Lloyd R. Snyder, Joseph J. Kirkland and John W.Dolan (2010) Introduction to Modern Liquid Chromatography, Third Edition A John Wiley & Sons Inc., chapter 7 page 331-337. 9.4 of Jan-Christer Janson (2011); Protein purification; Third edition; John Wiley & Sons Inc; chapter 4; 93-125. Page 3 10. www.amersham biosciences.com From, U. Rampriya - IICMS IICMS Newsletter IICMS-NL-12-006 Page 4 of 4