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Gas Chromatography PPT GCW.pptx

  1.  Rayat Shikshan Sansthas Veer Wajekar ASC College ,Phunde  Department of Chemistry T.Y.B.Sc. Analytical Chemistry Paper-IV Sem-VI CHROMATOGRAPHY Dr.Gurumeet C Wadhawa 29 March 2023 1
  2. Chromatography Chromatography - from Greek word chromos= colour and graphy= Writing Russian botanist- Mikhail Tswett (1903) Separation of plant pigment (Leaf extract) –Chlorophylls, xanthophylls Glass column packed with finely divided calcium carbonate stationary phase David Day- Geologist ,separation of crude oil on ( Fractional distribution) A.J.P. Martin and R.L.M. synge - 1952 Nobel Prize Separation,isolation,Identification of closely related components of Complex- mixture. All these methods involve the relative movement of two phases- stationary phase, Mobile phase
  3. Mikhail Tswett Born 14 May 1872 Asti, Italy Died 26 June 1919 (age 47) Nationality Russia Fields Botany Known for Adsorption chromatography
  4. Classification based on phases involved Solid Stationary Phase (Adsorption) Liquid Stationary Phase (Partition) Mobile phase liquid TLC Column Gel Mobile phase gas GSC Mobile Phase liquid Paper HPLC Mobile phase gas GLC
  5. Classification of Chromatographic methods According to mechanism of separation: The mechanism of separation depends mainly on the nature of the stationary phase. Based on separation mechanisms chromatography can be classified into: 1- Adsorption Chromatography: It is the oldest and most common type of chromatography. The stationary phase is a solid with adsorption power. Mixture components will be adsorbed on the surface of the stationary phase with different powers and that account for separation. Silica gel is the most common stationary phase in adsorption chromatography.
  6. Classification of Chromatographic methods According to mechanism of separation: The mechanism of separation depends mainly on the nature of the stationary phase. Based on separation mechanisms chromatography can be classified into: 1- Adsorption Chromatography: It is the oldest and most common type of chromatography. The stationary phase is a solid with adsorption power. Mixture components will be adsorbed on the surface of the stationary phase with different powers and that account for separation. Silica gel is the most common stationary phase in adsorption chromatography.
  7. 2- Partition Chromatography: The stationary phase is a liquid forming a thin film on an inert solid acts as support. The stationary liquid is usually more polar than the mobile liquid. The two liquids must be immiscible with each other. Cellulose powder and wet silica gel are examples of supports in partition chromatography that carry film of water act as stationary phase.
  8. 3- Ion Exchange Chromatography: Ion–exchange can be described as the process of the reversible stoichiometric exchange of ions of same charge between a mobile liquid phase and an insoluble solid stationary phase An ion exchanger is an insoluble material liberating the counter ions (mobile ions) by electrolytic dissociation.
  9. 4- Size –Exclusion Chromatography Gel filtration is used in fractionation mode, uses porous particles to separate multiple components in a sample on the basis of differences in their size. Molecules that are smaller than the pore size can enter the particles and therefore have a longer path and longer transit time than larger molecules that cannot enter the particles Schematic of a size-exclusion chromatography column
  10. GAS CHROMATOGRAPHY
  11. Contents  3.1.1 Introduction, Basic Principle, Terms involved in GC  (Numerical Problems Expected)  3.1.2 Instrumentation of Gas Chromatography: Block Diagram and  components.  3.1.3 Columns and their packing in GSC and GLC  3.1.4 Different types of detectors :TCD,FID,ECD  3.1.5 Quantitative and Qualitative analysis  3.1.6 Comparison between GSC and GLC  3.1.7 Applications of GC 29 March 2023 12
  12. Contents  3.1.1 Introduction, Basic Principle, Terms involved in GC  (Numerical Problems Expected)  3.1.2 Instrumentation of Gas Chromatography: Block Diagram and  components.  3.1.3 Columns and their packing in GSC and GLC  3.1.4 Different types of detectors :TCD,FID,ECD  3.1.5 Quantitative and Qualitative analysis  3.1.6 Comparison between GSC and GLC  3.1.7 Applications of GC 29 March 2023 13
  13. GAS SOLID CHROMATOGRAPHY SOLID + GAS GAS LIQUID CHROMATOGRAPHY LIQUID + GAS GAS CHROMATOGRAPHY ADSORPTION PARTITION 29 March 2023 14
  14. GLC at Glance Petroleum and refineries Food and Cosmetics Pharmaceuticals Environmental pollution control Forensic science Laboratories R&D Rubber Industries Polymer Industries And Many More 29 March 2023 15
  15. GAS CHROMATOGRAPHY THEORY INSTRUMENTATIONS APPLICATIONS 29 March 2023 16
  16. Partition Chromatography L+L Paper Chromatography L+L Gas Liquid Chromatography L+Gas HPLC L+ L 29 March 2023 17
  17. PRINCIPLE;- Gas chromatography consists of gas as mobile phase and stationary phase may be solid or liquid. The time require for the separation of component is decided by large no. of factor, but it primarily dependant on extent of adsorption of solute in GSC or its partition in liquid phase and gas mobile phase in GLC. If the solute shows more affinity for solid surface or liquid stationary phase it will take more time to move over the entire length of column i.e. it will take more time for separation and vice –versa. Consider a small length of column, sample contains three components A, B, and C is injected from sample injection port. It will be carried by mobile phase in the column. In the column the sample is get vaporized. The most volatile component will separate out first where as least volatile component will separate out later on. 29 March 2023 18
  18. The distribution coefficient shows the distribution of the molecules of the solute in two phases. Concentration of solute in the stationary phase Cs K= ------------------------------------------------------------------- = ------- CM Concentration of solute in the stationary phase A smaller value of K means that concentration of solute in mobile phase is more; it will require less time to come out from the column. Other hand a larger value of K means that concentration of solute in stationary phase is more; it will require more time to come out from the column. The time require to the elute the solute component from the column is called as Retention time, it’s a characteristic of every species .Qualitative analysis can be performed using retention time. Quantitative analysis can be performed from the area of the peak is calculated from the peak 29 March 2023 19
  19. Base line Retention Time------------ Detector Response Retention Time------------ B C A Chromatogram 29 March 2023 20
  20. In the operation of a gas chromatograph the, solutes in a mixture are completely vaporized in the injection port and they are moved through the column by a carrier gas under pressure. It is in the column where separation takes place. From the column, the separated solutes pass through a detector where they are sensed generating an electronic signal. The signal is then amplified and normally displayed on a strip chart recorder. The trace plotted on the recorder is called a "Chromatogram". It is a plot of the detector response in mini volts as a function of time. Usually, time is the abscissa and mini volts the ordinate. From the chromatogram, several general observations can be made. Under a given set of experimental conditions, each peak has a characteristic retention time (tR) and the retention volume (VR) that are useful in qualitative analysis of solutes. The retention time for solute A is depicted in the figure as the distance from 29 March 2023 21
  21. Important Terms Involved In GLC 29 March 2023 22
  22. a) Retention Time: (tR) It is used for qualitative analysis. It is defined as the time between the point of injection of sample and appearance of solute peak at the detector. OR The time require to the elute the solute component from the column Length of column Packing L Retention Time: (tR) =------------------------------- = ----------- Velocity of the solute Rs 29 March 2023 23
  23. b) Retention Volume: (VR): It is used for qualitative analysis. Volume of mobile phase requires to the solute component to elute from the column is called as Retention volume. Retention time and retention volume are related by equation, VR = tRF Where F is the flow rate of mobile phase Length of column Packing L Retention Volume: (VR) =-----------------------------------------------------------= ------- Velocity of the solute RS 29 March 2023 24
  24. C) Relative Retention: It is defined as the ratio of the retention time or retention volume for the substance, after correction for tM and VM to the corrected retention time or retention volume of a reference compound. tR – tM VR – VM O< =.------------- = ---------------------------- tRef– tM VRef – VM tR = Retention time of the substance . tM = Retention time of the mobile phase tRef = Retention time of the reference compound. VR = Retention volume of the substance. VM = Retention volume of the mobile phase VRef = Retention volume of the reference compound. 29 March 2023 25
  25. d) Height Equivalent to Theoretical Plate (HETP): Efficiency of column depends upon no. of theoretical plates that column is supposed to made of. HETP is length of column corresponding to a single theoretical plate. L HETP = -------- Where L= length of column. n n= number of theoretical plates ** An efficient column is one for which ‘n’ is large or ‘H; is small. 29 March 2023 26
  26. e) Peak resolution : Resolution is a measure of the separation between adjacent peaks in chromatogram *** As the difference between the retention time of the peaks increases, the separation increases i.e. Resolution is directly proportional to the difference in retention time of the peaks. 2[ (tR)2--(tR)1] Where (tR)1, (tR)2 are retention times R = --------------------------- of two peaks & W1+W2 are width W1+W2 of two peaks. 29 March 2023 27
  27. * * * * * * * carrier gas, Pressure regulator and flow control Sample Injection port column Column oven Recorder Detector GAS CHROMATOGRAPHIC INSTRUMENT * Most Volatile Least Volatile 29 March 2023 28
  28. Components of GLC Instruments Carrier Gas Flow control and Pressure Regualator Sample Injection Port Column Column Oven Detector Readout Device 29 March 2023 29
  29. • Characteristics Of a Carrier Gas 1 • It should be inert 2 • ii) It should be pure and dry. 3 • iii) It should not be inflammable 4 • iv) It should be chemically inert towards solutes of interest at the column temperature. 29 March 2023 30
  30. • The basic requirements of a liquid phase are as under 1 • It should exhibit different solubility for the components present in the mixture. 2 • ii) It should have low vapour pressure (0.01–0.1mm) at operating temperatures for a reasonable column life. 3 • iii) It should be thermally stable. 4 • iv) It should be chemically inert towards solutes of interest at the column temperature. 29 March 2023 31
  31. (+) (-) CATHODE ANODE Air COLUMN EFFLUENT H2 Collector Flame Electrical Igniter FLAME IONISATION DETECTOR FID 29 March 2023 32
  32. The principle of FID detector is, organic compound when reaches to flame produces ionic species that conduct electricity through flame. Hydrogen is as carrier gas in this detector. In FID the eluate coming from the column is combined with hydrogen (Fuel) and air to form combustible mixture. This mixture forms a flame which provides sufficient energy for ionization. The gaseous cations form in flame are attracted to negative electrode and repelled by positive electrode. Upon striking the collector electrode, the positive ion causes a current to flow in an external circuit. The current flow is proportional to the concentration of ionisable sample component. 29 March 2023 33
  33. Limitations of FID 1) FID responds to only ionisable substances. 2) It does not respond to inorganic compounds containing Nitrogen gas, oxygen gas and carbon dioxide gas. 3) It destroys the sample entered in to the flame. 29 March 2023 34
  34. Heated Metal Box THETHERMALCONDUCTIVITYDETECTOR Column Effluent In Column Effluent out Carrier Gas In Carrier Gas Out R S Leeds to Wheatstone bridge 29 March 2023 35
  35. The thermal conductivity detector is based on the difference between thermal conductivities of the pure gas and carrier gas containing sample. TCD consist of two identical brass cells fitted with platinum or tungsten wires. These resistance wires consist of reference and sensing elements which forms two arms of Wheatstone bridge. Both these wires are heated by an electric current. When pure carrier gas flows through both the cells, the temperature and hence resistance of both the filaments are in Wheatstone bridge is same which shows balanced circuit. 29 March 2023 36
  36. When column effluent allowed to flow through one cell and pure gas through the other cell, the resistance of both wire changes due to unequal cooling which results in increase in current. This current is directly proportional to the quantity of solute present in the sample. 29 March 2023 37
  37. Advantages of TCD: It response to organic and inorganic substances.  Its non destructive detector, the solute after separation can be collected.  It’s simple and gives large linear dynamic range 29 March 2023 38
  38. ELECTRON CAPTURE DETECTOR The basic principle of electron capture detector is based on electron absorption by compounds having an affinity for free electrons. It responds to compounds having an electronegative element or functional group. Methane gas is used in this detector because it easily undergoes ionization. In ECD Ni63 foil is used as source of beta rays. In presence of beta rays carrier gas undergoes ionization. This forms positive carrier gas ions and electrons. The electrons emitted during ionization are captured by positive collector electrode. When a sample component enters the detector, electrons emitted by carrier gas are captured by the component. The NET result is removal of electron from the system and decrease in standing current. The decrease current is recorded as negative peak on the recorder. 29 March 2023 39
  39. Column Effluent Collector Electrode Beta Source (+) (-) 29 March 2023 40
  40. Advantages Of ECD • It responds to compounds that capture the electrons. • Organic compound containing electronegative group’s ex. Nitro groups, phosphorous, oxygen and halogen. • ECD is very good detector for insecticides, pesticides, polychlorinated biphenyls. • It is non destructive in nature. 29 March 2023 41
  41. Advantages Of ECD It responds to compounds that capture the electrons.  Organic compound containing electronegative group’s ex. Nitro groups, phosphorous, oxygen and halogen.  ECD is very good detector for insecticides, pesticides, polychlorinated biphenyls.  It is non destructive in nature. 29 March 2023 42
  42. Applications of Gas Liquid Chromatography Qualitative Analysis Quantitative analysis Applications in various fields 29 March 2023 43
  43. Qualitative Analysis Retention Time Retention Volume 29 March 2023 44
  44. Quantitative analysis The chromatogram obtained on a recorder chart can be used to measure quantitatively the concentration of components in a mixture. In general, three methods are used for quantitative evaluation: i) Area normalization method: In this method, it is assumed that the entire sample is eluted from the column. The area of each peak is measured and percent composition is obtained by dividing the individual peak area by the total area of all the peaks and multiplying by 100. The value so obtained will be acceptable only if the detector response is the same (particularly for FED) for all the components of the mixture. If not, the detector response factor for each component needs to be established and appropriate corrections made in the measured areas. 29 March 2023 45
  45. i) Area normalization method: Area normalization method: Individual peak area Percentage Composition of Component= ------------------------------ X 100 • Total area of all the peaks 29 March 2023 46
  46. Internal Standardization method: In this method, known amounts of sample and standard are mixed and chromatographed. The peak areas for sample component and for standard are measured and ratios of both peak areas are determined. Either area ratios are plotted against weight ratios to obtain a graph. Chromatographor area ratios for unknown are compared directly with those for the known amounts. Thus, accurately known quantity of the internal standard is added the unknown sample and this mixture is chromatographed and area ratios are measured. 29 March 2023 47
  47. Comparison method: In this method, a synthetic mixture containing known quantities of the components of interest in the range of concentration expected in the unknown sample is prepared and analyzed. The values for the peak areas for different known volumes of synthetic blends are estimated and a calibration curve is plotted. An exact quantity of the unknown sample is then injected and the peak areas so calculated are used to read from the calibration curve the concentration of the component in the unknown mixture. 29 March 2023 48
  48. Other Applications 29 March 2023 49
  49. A) Bacterial identifications Long chain fatty acids found in the bacterial cell can be used to distinguish between various microorganisms. Fatty acids with chain length from Cl0 to C20 can be separated and estimated on a 3 m glass column of 2 mm internal diameter packed with 3% SP–2100 DOH at oven temperature of 150°C to 225°C with nitrogen gas at a flow rate of 20 rnL/min. 29 March 2023 50
  50. 2. Environmental analysis a) Water analysis: The organic pollutants in water are concentrated from water samples by solvent extraction or by purge and trap technique. The volatile pollutants are analysed on 80/100-mesh carbopack C/0.2 % carbowax 1500 column. 29 March 2023 51
  51. b) Air analysis: The analysis of organic vapours in the industrial air environment for the assessment of exposure to workers is done as follows: i) Organic vapours are collected on a charcoal adsorbent with a portable pump. ii) Desorption from charcoal is done in a closed vial with carbon disulphide. iii) Analysis of the desorbed sample is done on a GC using a 6 m, 3 mm internal diameter S.S column packed with 10 % SP–1000 by temperature programming from 100°C to 200°C. By this method, pollutants such as vinyl chloride, xylenes and aromatic hydrocarbons can be estimated. 29 March 2023 52
  52. c) Clinical and toxicological analysis Toxicologists have recognised the usefulness of GC for the analysis of toxic substances. The analysis of lidocaine and diphenhydramine has been done using flame ionisation detection. A 15m x 0.25mm i.d. 5% methylsilicone (DB-5) column has been used, temperature programmed from 180°C to 230°C at 5°C min–1 and helium used as a carrier gas. 29 March 2023 53
  53. Other Applications d) Forensic toxicology: It is highly specialized branch of analytical chemistry concerned primarily with the analysis of specimen from different organs of the human body for toxic substances. A simple GC system utilizing four columns and three liquid phases ( SE–30 , Hallcomid M-18, and Carbowax 6000), complemented by a direct solvent extraction scheme designed to detect common poisons, drugs, and human metabolites to a sensitivity limit of 2 μg/ml in blood, urine and tissue is developed. 29 March 2023 54
  54. •Thank you 29 March 2023 55
  55. Numerical based on Gas Chromatography UNIT 3
  56. Numerical 1 • Following data are obtained on a chromatographic column having a length of 30 cm – Retention time of unretained species = 1.40 min – Retention time of component X = 12.22 min – Bandwidth at the base = 1.5 min • Calculate – Average rate of movement of mobile phase – Average rate of movement of solute – Number of theoretical plate – HETP
  57. Solution 1 • Average rate of mobile phase( ) • Average rate of solute ( ) • Number of plates = • HETP =
  58. Numerical 2 • A chromatogram of a mixture A & B provided following data: • Calculate number of plates in each peak and HETP if column length is 25.0 cm Species Retention time (min) Peak width (min) Unretained 4.2 - A 6.4 1.75 B 9.0 2.07
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