Transcript
Page 1: Multidimensional chromatography

Multidimensional chromatography

The peak kapacity (z * y) if selectivity is different in the columns.

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Multidimensional chromatography with heart cut

Only few bandes are cut.

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Advantages of multidimensional chromatography

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Deans switch

The flow of mobile phase does not disturb by cut.No moving part are in the hot region.

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Deans switch

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Deans switches

No reactive surface in the flow pass.

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The advantage of Deans switch in trace analysis

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The sample focus in modulator

The sample is stopped (frozen) and focused in the modulator. The heating process is very fast.

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Coeluted peak separation in second dimension in GC xGC

The second column is very short . Elution time on it is equal with the collection time of next fraction.

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Analysis of chlorinated pesticides with GC x GC

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Analysis of gasoline with GC x GC

The first dimension is boiling point selective.Second dimension Π-Π interaction (aromatic) selective.

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HPLC frequently use off-line technique

The concentration of fraction, and the changing of mobile phase is easy with off-line.

Horváth Krisztián

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On-line coupling in HPLC

Collection from first column Transpher to second column

Horváth Krisztián

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Ortogonality

The anlysis is orthogonal, if their selectivity are based on different interactions

Same selectivitya Different selectivity Different selectivityDifferent pH Different stationary phase

Horváth Krisztián

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Corn oil 2D-HPLC

Horváth Krisztián

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HPLC/GC coupling

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HPLC/GC coupling

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HPLC X HPLC

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On-line coupling of chromatography - structure determination methods

• GC/MS, GC/FTIR

• HPLC/MS, HPLC/MS-MS, HPLC/FTIR, HPLC/NMR

• CE/MS, CE/MS-MS

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On-line LC/MS coupling

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Scan B

Magnetic sector mass spectometer

The bigger mass gives longer pass. Bigger charge give shorter pass.Everday practice the magnetic field is changed, to detect the ions in one point.

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Sheme of Quadrupol mass spectrometer

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Sheme of Quadrupol mass spectrometer

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Used ionization modes

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Electron impact ionzation (EI)

Generally the fragmentation energy is 70 eV.

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Fragmentation of EI

Quality measure is the (m/z) value.The quality measure the heigh of signals.The peak heigh is normalized for biggest peak (base peak, 100%).Certain compound has same fragmentation profile indepently from chromatographic.The quantitation is based on the area of total ion chromatogram (TIC) , or area of selected ions (SIM)

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Ilustration of fragmentation

The moleculs can be puzzle from fragmentogram.

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Fragmentation

The fragmentation is depend on the structure of analyte and fragmentation energy.

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Chemical ionization CI

1 Torr 10-6 Torr

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Chemical ionization (CI)• Pozitív (PCI) • NH3 + e -> NH4

+ + 2 e- • NH 4

+ + M > NH3 + [M+H] +

• NH 4 + + M > [M + NH4] +

• Negatív (NCI)• NH3 - e -> NH2

- • NH 2

- + M > NH2 + [M+H] -

• NH 2 + + M > [M + NH2] -

The pressure of CI is approximatelly 1 Torr. The reagents offer high and selective ionization . The CI is soft ionization having low fragmentation.

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GC-MS analysis with negative CI

Sensitivity has increased with electron capturing heptabutyrofluorid butane derivatives (HFBA)

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PCI vs. NCI

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Comparison of various ionization modes

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GC/MS on-line coupling

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Izotopselective GC/MS

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LC/MS couplings

The mobile phase has to be totally evaporatable.

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HPLC/MS electrospray ionization

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HPLC/MS electrospray ionization

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HPLC/MS with atmospheric pressure electrospray ionization

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MS-MS coupling

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Fast, selective analyses with LC/MS-MS

It is not necessary to separate compound, if they hace different fragmentation.

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Determination of herbicides with LC/MS-MS

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Ion trap MS

The ions are collected in parking circle.

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Total ion chromatogram (TIC) and selected ion monitoring (SIM)

The SIM is more sensitive than TIC with several magnitude.

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Comparison of TIC and (SIM)


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