Gas Chromatography
Gas Chromatography
Gas Chromatography
Gas chromatography is a technique used for separation of volatile substances, or substances that can be made volatile, from one another in a gaseous mixture at high temperatures. A sample containing the materials to be separated is injected into the gas chromatograph. A mobile phase (carrier gas) moves through a column that contains a wall coated or granular solid coated stationary phase. As the carrier gas flows through the column, the components of the sample come in contact with the stationary phase. The different components of the sample have different affinities for the stationary phase, which results in differential migration of solutes, thus leading to separation
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Martin and James introduced this separation technique in 1952, which is the latest of the major chromatograhpic techniques. However, by 1965 over 18000 publications in gas chromatography (GC) were available in the literature. This is because optimized instrumentation was feasible. Gas chromatography is good only for volatile compounds or those, which can be made volatile by suitable derivatization methods or pyrolysis. Thus, about 20% of chemicals available can be analyzed directly by GC.
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Gas chromatography can be used for both qualitative and quantitative analysis. Comparison of retention times can be used to identify materials in the sample by comparing retention times of peaks in a sample to retention times for standards. The same limitations for qualitative analysis discussed in Chapter 26 also apply for separations in GC. Quantitative analysis is accomplished by measurement of either peak height or peak area
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Instrumentation
It may be wise to introduce instrumental components before proceeding further in theoretical background. This will help clarify many points, which may, otherwise, seem vague. It should also be noted that a detector will require special gas cylinders depending on the detector type utilized. The column temperature controller is simply an oven, the temperature of which can be varied or programmed
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Syringe Injector
Detector
Flow Controller
Column
Three temperature zones can be identified: 1. Injector temperature, TI, where TI should allow flash vaporization of all sample components. 2. Column temperature, Tc, which is adjusted as the average boiling points of sample components. 3. Detector Temperature, TD, which should exclude any possible condensation inside the detector. Generally, an intuitive equation can be used to adjust all three zones depending on the average boiling point of the sample components. This equation is formulated as: TI = TD = Tc + 50 oC
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The Carrier Gas Unlike liquid chromatography where wide varieties of mobile phase compositions are possible, mobile phases in gas chromatography are very limited. Only slight changes between carrier gases can be identified which places real limitations to chromatographic enhancement by change or modification of carrier gases
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A carrier gas should have the following properties: 1. Highly pure (> 99.9%) 2. Inert so that no reaction with stationary phase or instrumental components can take place, especially at high temperatures. 3. A higher density (larger viscosity) carrier gas is preferred. 4. Compatible with the detector since some detectors require the use of a specific carrier gas. 5. A cheap and available carrier gas is an advantage.
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The same van Deemter equation as in LC can be written for GC where: H = A + B/V + CV The optimum carrier gas velocity is given by the derivative of van Deemter equation Vopt = { B/C }1/2
However, the obtained velocity is much greater than that obtained in LC.
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The carrier gas pressure ranges from 10-50 psi. Higher pressures potentially increase compression possibility while very low pressures result in large band broadening due to diffusion. Depending on the column dimensions, flow rates from 1-150 mL/min are reported. Conventional analytical columns (1/8) usually use flow rates in the range from 20-50 mL/min while capillary columns use flow rates from 1-5 mL/min depending on the dimensions and nature of column. In most cases, a selection between helium and nitrogen is made as these two gases are the most versatile and common carrier gases in GC.
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Injectors
Septum type injectors are the most common. These are composed of a glass tube where vaporization of the sample takes place. The sample is introduced into the injector through a self-sealing silicone rubber septum. The carrier gas flows through the injector carrying vaporized solutes. The temperature of the injector should be adjusted so that flash vaporization of all solutes occurs. If the temperature of the injector is not high enough (at least 50 degrees above highest boiling component), band broadening will take place.
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Syringe Septum
To Column
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Packed columns are made of stainless steel or glass while open tubular columns are usually made of fused silica. The temperature of the column is adjusted so that it is close to the average boiling point of the sample mixture. However, temperature programming is used very often to achieve better separations. The temperature of the column is assumed to be the same as the oven which houses the column. The oven temperature should be stable and easily changed in order to obtain reproducible results.
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Detection Systems
Several detectors are available for use in GC. Each detector has its own characteristics and features as well as drawbacks. Properties of an ideal detector include:
1. 2. 3. 4. 5. 6. 7. 8. 9. High sensitivity Minimum drift Wide dynamic range Operational temperatures up to 400 oC. Fast response time Same response factor for all solutes Good reliability (no fooling) Nondestructive Responds to all solutes (universal)
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Note that gases should always be flowing through the detector including just before, and few minutes after, the operation of the detector. Otherwise, the filament will melt. Also, keep away any oxygen since oxygen will oxidize the filament and results in its destruction.
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Remember that TCD characteristics include: 1. Rugged 2. Wide dynamic range (105) 3. Nondestructive 4. Insensitive (10-8 g/s) 5. Flow rate sensitive
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The FID detector is a mass sensitive detector where solutes are ionized in the flame and electrons emitted are attracted by a positive electrode, where a current is obtained. The FID detector is not responsive to air, water, carbon disulfide. This is an extremely important advantage where volatile solutes present in water matrix can be easily analyzed without any pretreatment.
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Remember that FID characteristics include: Rugged Sensitive (10-13 g/s) Wide dynamic range (107) Signal depends on number of carbon atoms in organic analytes which is referred to as mass sensitive rather than concentration sensitive Weakly sensitive to carbonyl, amine, alcohol, amine groups Not sensitive to non-combustibles H2O, CO2, SO2, NOx Destructive
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Remember the following facts about ECD: 1. Electrons from a b-source ionize the carrier gas (nitrogen) 2. Organic molecules containing electronegative atoms capture electrons and decrease current 3. Simple and reliable 4. Sensitive (10-15 g/s) to electronegative groups (halogens) 5. Largely non-destructive 6. Insensitive to amines, alcohols and hydrocarbons 7. Limited dynamic range (102) 8. Mass sensitive detector
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Several types of tubing were used ranging from copper, stainless steel, aluminum and glass. Stainless steel is the most widely used because it is most inert and easy to work with. The column diameters currently in use are ordinarily 1/16" to 1/4" 0.D. Columns exceeding 1/8" are usually used for preparative work while the 1/8" or narrower columns have excellent working properties and yield excellent results in the analytical range. These find excellent and wide use because of easy packing and good routine separation characteristics. Column length can be from few feet for packed columns to more than 100 ft for capillary columns.
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Capillary/Open Tubular
Open tubular or capillary columns are finding broad applications. These are mainly of two types: Wall-coated open tubular (WCOT) <1 mm thick liquid coating on inside of silica tube Support-coated open tubular (SCOT) 30 mm thick coating of liquid coated support on inside of silica tube These are used for fast and efficient separations but are good only for small samples. The most frequently used capillary column, nowadays, is the fused silica open tubular column (FSOT), which is a WCOT column.
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The external surface of the fused silica columns is coated with a polyimide film to increase their strength. The most frequently used internal diameters occur in the range from 260-320 micrometer. However, other larger diameters are known where a 530 micrometer fused silica open tubular column was recently made and is called a megapore column, to distinguish it from other capillary columns. Megapore columns tolerate a larger sample size.
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It should be noted that since capillary columns are not packed with any solid support, but rather a very thin film of stationary phase which adheres to the internal surface of the tubing, the A term in the van Deemter equation which stands for multiple path effects is zero and the equation for capillary columns becomes H = B/V + CV
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Capillary columns advantages compared to packed columns 1. higher resolution 2. shorter analysis times 3. greater sensitivity
Capillary columns disadvantage compared to packed columns 1. smaller sample capacity
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% Loading =
Weight of liquid stationary phase * 100% Weight of stationary phase plus solid support
Increasing percent loading would allow for increased sample capacity and cover any active sites on the solid support. These two advantages are very important, however increasing the thickness of stationary phase will affect the C term in the van Deemter equation by increasing HS, and therefore Ht.
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Generally, the film thickness primarily affects the retention character and the sample capacity of a column. Thick films are used with highly volatile analytes, because such films retain solutes for a longer time and thus provide a greater time for separation to take place. Thin films are useful for separating species of low volatility in a reasonable time. On the other hand, a thicker film can tolerate a larger sample size. Film thicknesses in the range from 0.1 5 mm are common.
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The polarity of the stationary phase can be changed by derivatization with different functional groups such as a phenyl group. Bleeding of the column is cured by bonding the stationary phase to the column; or crosslinking the stationary phase.
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Liquid Stationary Phases should have the following characteristics: Low volatility High decomposition temperature (thermally stable) Chemically inert (reversible interactions with solvent) Chemically attached to support (to prevent bleeding) Appropriate k' and a for good resolution
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In summary, stationary phases are usually bonded and/or crosslinked and the following remarks are usually helpful: 1. Bonding occurs through covalent linking of stationary phase to support 2. Crosslinking occurs through polymerization reactions to join individual stationary phase molecules 3. Nonpolar stationary phases are best for nonpolar analytes where nonpolar analytes are retained preferentially 4. Polar stationary phases are best for polar analytes where polar analytes are retained preferentially
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Open tubular capillary columns, either WCOT, SCOT are routinely used. In WCOT the capillary is coated with a thin film (0.1-0.25 mm) of the liquid stationary phase while in SCOT a thin film of solid support material is first affixed to the inner surface of the column then the support is coated with the stationary phase. WCOT columns are most widely used. Capillary columns are typically made from fused silica (FSOT) and are 15 to 100 m long with 0.10 to 0.5 mm i.d.
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The thickness of the stationary phase affects the performance of the column as follows:
1. Increasing thickness of stationary phase allows the separation of larger sample sizes. 2. Increasing thickness of stationary phase reduces efficiency since HS increases. 3. Increasing thickness of stationary phase is better for separation of highly volatile compounds due to increased retention.
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Much more efficient separations can be achieved with capillary columns, as compared to packed columns, due to the following reasons: 1. Very long capillary columns can be used which increases efficiency 2. Thinner stationary phase films can be used with capillary columns 3. No eddy diffusion term (multiple paths effect) is observed in capillary columns
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Temperature Programming
Gas chromatographs are usually capable of performing what is known as temperature programming gas chromatography (TPGC). The temperature of the column is changed according to a preset temperature isotherm. TPGC is a very important procedure, which is used for the attainment of excellent looking chromatograms in the least time possible. For example, assume a chromatogram obtained using isothermal GC at 80 oC, as shown below:
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It is clear from the figure that the separation is optimized for the elution of the first two components. However, the last two components have very long retention and appear as broad peaks. Using isothermal conditions at high temperature (say for example 200oC) can optimize the elution of the last two compounds but, unfortunately, results in bad resolution of the earlier eluting compounds as shown in the figure below where the first two components are coeluted while the resolution of the second two components becomes too bad:
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One can also optimize the separation of the middle too components by adjusting the isothermal conditions (for example at say 160 oC). In this case, a chromatogram like the one below can be obtained:
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However, in chromatographic separations we are interested in fully separating all components in an acceptable resolution. Therefore, it is not acceptable to optimize the separation for a single component while disregarding the others. The solution of this problem can be achieved by consecutive optimization of individual components as the separation proceeds. In this case, temperature should be changed during the separation process. This is called temperature programming gas chromatography (TPGC)
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First, a temperature suitable for the separation of the first eluting component is selected, and then the temperature is increased so that the second component is separated and so on. The change in temperature can be linear, parabolic, step, or any other formula. The chromatographic separation where the temperature is changed during the elution process is called TPGC. A separation like the one below can be obtained:
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Temperature Zones in GC
Three temperature zones should be adjusted before a GC separation can be done. The injector temperature should be such that fast evaporation of all sample components is achieved. The temperature of the injector is always more than that of the column, which depends on the operational mode of the separation. The detector temperature should be kept at some level so as to prevent any solute condensation in the vicinity of the detector body.
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Molecular Sieves
Molecular sieves are metal aluminum silicate ion exchangers, whose pore size depends upon the kind of cation present, like sodium in sodium aluminum silicate molecular sieves. The sieves are classified according to the maximum diameter of molecules that can enter the pores. Commercial molecular sieves come in pore sizes of 4, 5, 10, and 13 angstroms. Molecular sieves can be used to separate small molecules from large ones.
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Porous Polymers
Porous polymer beads of uniform size are manufactured from styrene crosslinked with divinylbenzene. The pore size of these beads is uniform and is controlled by the amount of crosslinking. Porous polymers have found considerable use in the separation of gaseous species such as hydrogen sulfide, oxides of nitrogen, water, carbon dioxide, methanol, etc.
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Quantitative Analysis
GC is an excellent quantitative technique where peak height or area is proportional to analyte concentration. Thus the GC can be calibrated with several standards and a calibration curve is obtained, then the concentration of the unknown analyte can be determined using the peak area or height. The detector response factor for each analyte should be considered for accurate quantitative analysis.
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Gas chromatographs are widely used as criteria for establishing the purity of organic compounds. Contaminants, if present, are revealed by the appearance of additional peaks. Qualitative Analysis is usually done by comparison with retention times of standards, which are very reproducible in GC, provided good injection practices are followed. Injection should be done with a suitable Hamilton type syringe through the heated septum injector till all needle disappears, then the needle is drawn back as steadily and fast as possible. This is important for reproducible attainment of retention times.
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By definition, the retention index for a normal alkane is equal to 100 times the number of carbons in the compound regardless of the column packing, the temperature, or other chromatographic conditions. The retention index system has the advantage of being based upon readily available reference materials that cover a wide boiling range. The retention index of a compound is constant for a certain stationary phase but can be totally different for other stationary phases.
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In finding the retention index, a plot of the number of carbons of standard alkanes against the logarithm of the adjusted retention time is first constructed. The value of the logarithm of the adjusted retention time of the unknown is then calculated and the retention index is obtained from the plot. The adjusted retention time, tR, is defined as: tR = tR - tM
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Mass Spectrometry
O H3C C N C O N H C C C H3 N C H N Mass Spectrometer
Mass Spectrum
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55 82 42
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Mass (amu)
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