theoretical background gas chromatography hplc columns and interactions
TRANSCRIPT
![Page 1: Theoretical Background Gas Chromatography HPLC Columns and Interactions](https://reader033.vdocuments.mx/reader033/viewer/2022051216/5697c0261a28abf838cd5918/html5/thumbnails/1.jpg)
Best Broken into four categories
Theoretical Background
Gas Chromatography
HPLC Columns and Interactions
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HPLCHigh Performance Liquid Chromatograpy
Use for: Small molecules
o Charged, Neutral, Hydrophillic, Hydrophobic Large molecules
o Synthetic polymers, proteins, carbohydrates Thermolabile molecules
Must be soluble in mobile phase
Not used for: Gasses Very small simple molecules
o Alkanes
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HPLC Setup
1
• Mobile Phase Reservoir• Degasser
2• Pump
3
• Injector• Autosampler
4
• Column• In optional oven
5• Detector
6
• Recorder • PC
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Mobile Phase Reservoir
Mixture of Different SolventsExamples: Organic, Buffers, Water
Methanol, Ethanol, Acetonitrile, Hexane, DCMBuffers: Phosphate, Acetate, Formate
All solvents must be HPLC quality grade (Extremely pure)
Before use the mobile phase must be Filtered through fine filters to remove any particles from solvents Degassed
o Remove dissolved gas from the solution• Vacuum Degasser• Helium as a degassing gas
1• Mobile Phase Reservoir
• Degasser2• Pump
3• Injector
• Autosampler4
• Column• In optional oven
5• Detector
6• Recorder
• PC
![Page 5: Theoretical Background Gas Chromatography HPLC Columns and Interactions](https://reader033.vdocuments.mx/reader033/viewer/2022051216/5697c0261a28abf838cd5918/html5/thumbnails/5.jpg)
Pumps
Pumps for HPLC need to be: Able to pump at high pressure Very precise control of flow rate
Isocratic ElutionUse of single solvent or mixed solvent of constant compositionGradient ElutionTwo pumps, or one pump and proportioning valve, used to deliver changing mixture of two or more solventsUseful to achieve better separation and shorter elution times by creating mobile phase gradients
1• Mobile Phase Reservoir
• Degasser2• Pump
3• Injector
• Autosampler4
• Column• In optional oven
5• Detector
6• Recorder
• PC
![Page 6: Theoretical Background Gas Chromatography HPLC Columns and Interactions](https://reader033.vdocuments.mx/reader033/viewer/2022051216/5697c0261a28abf838cd5918/html5/thumbnails/6.jpg)
Injectors
Introduces sample to systemDifficult as under high pressure
Direct injection is difficult
Two types of injectors: Manual Auto Sampler
Sample loop fixes the exact quantity of sample to be injected each time
1• Mobile Phase Reservoir
• Degasser2• Pump
3• Injector
• Autosampler4
• Column• In optional oven
5• Detector
6• Recorder
• PC
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Column
Contains stationary phase particlesUsually made from stainless steel or plastic
Pre-Columns, Guard Cartridge, used either to: Protect column
o Same stationary phase Pre-separate sample
o Different stationary phase
Once activated:Washed after use, and kept in solvent
1• Mobile Phase Reservoir
• Degasser2• Pump
3• Injector
• Autosampler4
• Column• In optional oven
5• Detector
6• Recorder
• PC
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Column
Stationary Phases
Normal Phases NP Polar Stationary Phases
o Silica, Alumina Adsorption Chromatography
Reversed Phases RP Non-polar Stationary Phases Polar Stationary Phases
Bonded silica, C2, C4, C8, C18
Absorption / Partition Chromatography
pH Sensitive (Between pH 2 to 8)Silica is slightly soluble at alkaline pH
1• Mobile Phase Reservoir
• Degasser2• Pump
3• Injector
• Autosampler4
• Column• In optional oven
5• Detector
6• Recorder
• PC
Requirements Column must be equilibrated
before separation process Shorter Narrower tubing
reduces dead volume (extra column volume)
OvensRetention time temperature dependantTwo injections of same sample can be significant in temperature changesOven maintains temperature
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Detectors
ExamplesUltraviolet and Visible absorptionDifferential refractive indexElectrochemical: AmperometricElectrochemical: ConductometricFluorescenceMass SpectrometrySolution Light ScatteringEvaporative Light Scattering
1• Mobile Phase Reservoir
• Degasser2• Pump
3• Injector
• Autosampler4
• Column• In optional oven
5• Detector
6• Recorder
• PC
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Detectors
UV/VIS DetectorsDiode Array Detector (DAD)
1• Mobile Phase Reservoir
• Degasser2• Pump
3• Injector
• Autosampler4
• Column• In optional oven
5• Detector
6• Recorder
• PC
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Detectors
UV/VIS DetectorsPhoto Diode Array Detector
Peak Purity Comparison of spectra
at three different points of peak elution time (start, middle, end)
If identical three spectra identical
1• Mobile Phase Reservoir
• Degasser2• Pump
3• Injector
• Autosampler4
• Column• In optional oven
5• Detector
6• Recorder
• PC
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Detectors
Refractive Index Detectors
UniversalBulk Property Good for polymersGood for analytes with no chromophores
1000 times less sensitive than UVUseless in gradient elutionSensitive to temperature and pressureNot good for trace analysis
1• Mobile Phase Reservoir
• Degasser2• Pump
3• Injector
• Autosampler4
• Column• In optional oven
5• Detector
6• Recorder
• PC
![Page 13: Theoretical Background Gas Chromatography HPLC Columns and Interactions](https://reader033.vdocuments.mx/reader033/viewer/2022051216/5697c0261a28abf838cd5918/html5/thumbnails/13.jpg)
Sample PreparationSample must be soluble in mobile phaseOverload of sample may damage columnConcentration of key analytes should be in linear range of detectorQuantity of sample introduced to system depends on sample loop sizeSeparated compounds can be collected and isolated after detection point (if not destroyed)
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Separation Process - Parameters
Column LengthLonger Column, Better Separation, Longer Retention TimeParticle Size of Stationary PhaseSmaller Particles, Narrower Peaks, Higher PressuresTemperatureHigher Temperature, Faster Diffusion, Better Separation, Shorter Retention Times, Column DegradesCombination of Mobile PhasesGradient Elution, Best Separation, Shortest TimepH of Mobile PhaseIonised compounds not retained well on RP-Columns
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Best Broken into four categories
Theoretical Background
Gas Chromatography
HPLC Columns and Interactions
![Page 16: Theoretical Background Gas Chromatography HPLC Columns and Interactions](https://reader033.vdocuments.mx/reader033/viewer/2022051216/5697c0261a28abf838cd5918/html5/thumbnails/16.jpg)
Effect of Particle SizeSmaller Particles increases Efficiency due to Sharper Peaks!More theoretical plates N, smaller HETP h.Smaller Particles need Higher Pressure to force mobile phase through columnMaximum flow rates are limited by high pressures
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Silica SurfaceDominated by Polar Functional Groups
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Reversed – Phase SilicaAcid condensation of silica forms RP silicaHydrophobic molecules bonded to silica surfaceSwitches to a non-polar environment
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Analyte Interactions
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Silica SurfacePolar
NP
Silica SurfaceNonPolar
RP
What do you expect to happen when red line breaks?
Blue solvent: Water
RP vs NP
Like Attract LikeOpposite Phases
Repel
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NP vs RP
Like Attracts Like
Solvents with similar functionalities to the analytes will adsorb in the same way and compete for the same interaction sites. This will effect the binding equilibrium
Reversed Phase Silica is more common
Why?Better Peak ShapeLess Tailing due to strong interactionsAqueous content of mobile phase allows bufferingControl analyte ionisation with pHBetter Control of mobile phase gradientsComposition varies more widely
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LastFirst
Predicting the Order of Elution
Identify key points of differencePolarityMore Polar = Stronger Interaction in Normal PhaseMore Polar = Weaker Interaction in Reversed Phase
What is eluted first in a Normal Phase Column?Opposite applies for Reversed Phase
OH
OH
O
N
O
OH
O
N
O
O
O
N
O
O
Morphine Codine Heroin
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Effect of Stationary Phase
For reverse phase silicaLonger chain lengths result in longer elution times and better resolution
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Effect of Mobile PhaseFor reverse phase silica
Increasing the proportion of ‘weak ‘ solvent reduces competition for adsorption – analytes are retained longer and resolved better
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Optimising Mobile Phase
If some analytes are insufficiently retained while others are excessively retained, vary strength of mobile phase!
Use of gradients allow peaks at certain intervals to spread or narrow giving good resolution and improve overall run time
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Effect of Mobile Phase pH
General RuleAnalytes should be uncharged
Low pH for acidsHigh pH for bases
BUT! Remember silica has limited stability at high and low pH.