Lecture 5 - coupling considerations Flashcards

1
Q

What does each detector detect and is it destructive?

A

Flame ionization detector - Carbon compounds and yes
Flame photometric detector - Sulphur, P and halogenated compounds and yes
Mass spectrometry - ionized molecular fragments and yes
Nitrogen-phosphorus detector - N, P and halogenated compounds and yes
Atomic-emission detector - yes

Thermal conductivity detector - thermal conductivity and no
Electron capture device - electronegative groups and no

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2
Q

How does the FID work?

A
  • Heats analyte in H flame and component in analyte loses electron. Unselective and widely used.
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3
Q

How does the FPD work?

A
  • Involves burning compound in a flame. A photomultiplier tube is then used to detect lines as specific elements emit light. More specific than FID so less analytes can be used.
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4
Q

How does TCD work?

A
  • Helium or H used as a standard, has a response to all compounds as they all have a different thermal conductivity from helium and H.
  • There are 2 parallel tubes containing the reference gas and sample (in heating coils).
  • It compares the heat loss rate from sample into reference gas, compares the changes in TC of the sample to reference flow of carrier gas.
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5
Q

How does MS work?

A
  • In GC-MS packed columns are used but with flow rates of 20-30 mL min-1. To reduce large flow rates a jet separator is used.
  • A vacuum is used to allow sample to be put into an inlet system, while keeping the rest of the S under vacuum.
  • Not ideal for detecting tiny molecules.
  • GC and MS can be combined as during GC the sample is already in a capillary tube which is needed for MS.
  • Systems now contain HP pumping systems.
  • Flow rates now <5 mL or less, a direct interface is possible.
  • Bench top systems now can handle these easily, are more sensitive and give better preservation of GC results.
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6
Q

What are the detectors coupled with LC?

A
  • Mass spec which is destructive and detects ions.
  • Optical detection (can be UV/vis or fluorescent compounds) which is non-destructive.
  • Refractive index which is non-destructive and detects all compounds.
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7
Q

How does the spectroscopic detection work?

A
  • By emission (fluorescence) or absorbance (UV) analyte.
  • For UV/vis abs is plotted against elution time (min)
  • For fluorescence % flu is plotted against elution time (min)
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8
Q

How does refractive index work?

A
  • A beam irradiates the cell.
  • When only a MP is present the beam will be straight and wont reflect, when a sample is added in the beam will bend.
  • A reflex index difference is then found.
  • Has a lower sensitivity than UV and used for samples which don’t abord UV, like alcohols, sugars or inorganic ions.
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9
Q

How is the conductivity detector used?

A
  • Measure the ability to pass an electric current by recording electronic resistance. Also, electrochemical measurements such as amperometry, voltammetry, coulometry
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10
Q

How does MS-LC work?

A

Samples A, B and C injected into HPLC (A is sample of interest). HPLC will separate sample A, then MS ion source will split A into its corresponding ion fragments. Then the mass analyser will sort these corresponding to mass/z ratio.

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11
Q

What are the problems with LC-MS?

A
  • Large volume of MP
  • Buffers and additives cause problems for MS ionisation (these must be volatile to reduce these effects)
  • Large flow rates and low sample concs
  • Liquid samples need to be vaporised first
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12
Q

How does electrospray work? and how does ACPI differ?

A

Analyte flows through capillary, the solution is then drawn out in a cone shape which become droplets. The droplets progressively get smaller and smaller. The droplets vaporise rapidly and only gas-phase ions remain which then go to detector
ACPI uses a UV light to separate the analyte ions from the solvent

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13
Q

Why are UHPLC systems now being used?

A
  • Flow rates are 0.01 - 3 mL min-1 and up to 15000 psi.
  • They have sub 2 um particles which permit faster separations, higher resolution and unmatched efficiency.
  • Needs low volumes (25 mL)
  • These separations can be done in 5 mins.
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