Gas Chromatography.

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Presentation transcript:

Gas Chromatography

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

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

History of Chromatography 1903 - Mikhail Tswett separated plant pigments using paper chromatography liquid-solid chromatography 1930’s - Schuftan & Eucken use vapor as the mobile phase gas solid chromatography

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

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)

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

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

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

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)

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

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

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

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

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

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

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…

Temperature Control Options Example Method Column: Petrocol DH, 100m x 0.25mm ID, 0.5µm film Cat. No.: 24160-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