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Gas Chromatography.

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Presentation on theme: "Gas Chromatography."— Presentation transcript:

1 Gas Chromatography

2 Gas Chromatograph: an overview
What is “chromatography” History of chromatography Applications Theory of operation Detectors Syringe technique

3 What is “Chromatography”
“color writing” the separation of mixtures into their constituents by preferential adsorption by a solid” (Random House College Dictionary, 1988) “Chromatography is a physical method of separation in which the components to be separated are distributed between two phases, one of the phases constituting a ______________ of large surface area, the other being a ______ that percolates through or along the stationary bed.” (Ettre & Zlatkis, 1967, “The Practice of Gas Chromatography) stationary bed fluid

4 History of Chromatography
Mikhail Tswett separated plant pigments using paper chromatography liquid-solid chromatography 1930’s - Schuftan & Eucken use vapor as the mobile phase gas solid chromatography

5 Applications gas Compound must exist as a ____ at a temperature that can be produced by the GC and withstood by the column (up to 450°C) Alcohols in blood Aromatics (benzene, toluene, ethylbenzene, xylene) Flavors and Fragrances Permanent gases (H2, N2, O2, Ar, CO2, CO, CH4) Hydrocarbons Pesticides, Herbicides, PCBs, and Dioxins Solvents

6 Advantages of Gas Chromatography
Requires only very small samples with little preparation Good at separating complex mixtures into components Results are rapidly obtained (1 to 100 minutes) Very high precision Only instrument with the sensitivity to detect volatile organic mixtures of low concentrations Equipment is not very complex (sophisticated oven)

7 Theory of Operation Velocity of a compound through the column depends upon affinity for the stationary phase Area under curve is ______ of compound adsorbed to stationary phase mass Carrier gas Gas phase concentration

8 Process Flow Schematic
Detector (flame ionization detector or FID) Sample injection Carrier gas (nitrogen or helium) Air Hydrogen Long Column (30 m)

9 Gas Chromatograph Components
top view Flame Ionization Detector Injection Port Column Oven front view

10 Flame Ionization Detector
Teflon insulating ring Coaxial cable to Analog to Digital converter Gas outlet Collector Ions Flame Sintered disk Platinum jet Air Hydrogen Why do we need hydrogen? Capillary tube (column)

11 Flame Ionization Detector
Responds to compounds that produce ____ when burned in an H2-air flame all organic compounds Little or no response to (use a Thermal Conductivity Detector for these gases) CO, CO2, CS2, O2, H2O, NH3, inert gasses Linear from the minimum detectable limit through concentrations ____ times the minimum detectable limit ions 107

12 Gas Chromatograph Output
Peak ____ proportional to mass of compound injected Peak time dependent on ______ through column area velocity detector output time (s)

13 Other Detectors low Thermal Conductivity Detector
Difference in thermal conductivity between the carrier gas and sample gas causes a voltage output Ideal carrier gas has a very ____ thermal conductivity (He) Electron Capture Detector Specific for halogenated organics low

14 Advantage of Selective Detectors
TCE Mixture containing lots of methane and a small amount of TCE FID output methane time ECD output time

15 Mass Spec Output mass-to-charge ratio
Each peak of a chromatogram becomes a “fingerprint” of the compound The fingerprints are compared with a library to identify the compounds mass-to-charge ratio

16 Purge and Trap Way to measure dilute samples by concentration of constituents Trap constituents under low temperature Heat trap to release constituents and send to GC column N2 Trap

17 Techniques to Speed Analysis
Problem: some components of a mixture may have very high velocities and others extremely low velocities. slow down fast components so they can be separated speed up slow components so analysis doesn’t take forever Solution…

18 Temperature Control Options
Example Method Column: Petrocol DH, 100m x 0.25mm ID, 0.5µm film Cat. No.: U Oven: 35°C (15 min) to 200°C at 2°C/min, hold 5 min Carrier: helium, 20cm/sec (set at 35°C) Det.: FID, 250°C Inj.: 0.1µL premium unleaded gasoline, split (100:1), 250°C


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