Midterm 2 Review Flashcards

1
Q

What are ICP, ESI and MALDI used for?

A

Volatilization and ionization

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2
Q

What are EI and CI used for?

A

Ionization

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3
Q

What are quadrupole, TOF, fourier transform and ion traps used for?

A

Mass sorting

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4
Q

What are electron multipliers used for?

A

Detection

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5
Q

Isobaric Interference?

A

Results from equal mass isotopes of different elements present in sample solution

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6
Q

How to correct isobaric interference?

A

Use relative gas that forms product with similar mass to that of the unwanted isotope

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7
Q

Polyatomic Interference?

A

Combination of two or more isotopes from different elements in the same plasma

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8
Q

How to correct polyatomic interference?

A

Use hexapole collision cell to remove unwanted molecules

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9
Q

What are the 4 components of mass spec?

A

Sample inlet/volatilization
An ionization source
A mass analyzer
detector

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10
Q

ICP Torch

A

very very hot and makes ions to use in MS. Analyte must be separated before entering ICP. Laser adsorption to produce ions. Plasma detected through cooling cone. Extraction lens attracts positive ions from plasma. Ions enter collision cell (with H2 or He). Ions guided to mass spec

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11
Q

Interphase in MS?

A

Transport as many ions as possible to MS while excluding photons, neutrons and other unwanted particles that will produce unwanted signal.

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12
Q

Quadrupole advantages and disadvantages

A

compact, tough, cheap, high scan rate, BEST sensitivity

WORST resolution, slow, maximum ratio

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13
Q

Time of flight advantages and disadvantages

A

Simple, can combine with many ion sources, unlimited mass range, FAST

low sensitivity and resolution

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14
Q

Double focusing advantages and disadvantages

A

BEST resolution, double focuses

Huge and expensive, requires extensive knowledge to operate

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15
Q

3 main uses of MS

A
  1. Analysis of pure compound (give molecular mass, dormula, isotopic ratio, fragmentation patterns
  2. Mixture analysis (requires separation using GC-MS, LC-MS, CE-MS)
  3. Quantification (requires internal standards and cal curve)
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16
Q

Applications for molecular MS

A

pharmaceutical analysis, forensics, food safety

17
Q

Electron impact advantages and disadvantages

A

Cheap, touch, reproducible

rough on molecule, molecular ions do not survive, entire class of compounds does not work

18
Q

Exact Mass?

A

Calculated

19
Q

Accurate mass?

A

Actual measured m/z

20
Q

Chemical ionization?

A

a gaseous reagent is introduced into ionization region. Ionized carrier gas with EI and collides gas with analyte

21
Q

CI advantages and disadvantages

A

nice and gentle, molecular ion will survive, cheap

Molecule must be volatile, not reproducible, low polarity requires

22
Q

Electrospray Ionization (ESI)

A

used for large molecules where fragmentation is avoided.
Dispersal of fine spray charges droplets followed by solvent evaporation and ion ejection. Sample is injected into high voltage capillary and comes out as a highly charges mist. Solvent evaporated with N2. Molecular ions then repel each other and charged analyte is ejected into mass analyzer.

23
Q

Matrix Assisted Laser Desorption ionization (MALDI)

A

Analyte is mixed in matrix solvent and applied to metal plate. A laser light hits causing energy absorption. The analyte is ionized and ejected into gas phase and is then accelerated into chosen MS.

Very expensive but has HIGHEST m/z ratio

24
Q

Fourier transform ion-cyclotron MS (FTIC)

A

Used a magnetic field to trap ions into an orbit (centripetal force).

25
Q

Multiple reaction monitoring (MRM) vs Selected “” (SRM) vs product ion scan (PIS)

A

MRM/SRM monitors each precursor ion/product ion transition at a time.

SRM is monitoring only a single fixed mass window
MRM scans rapidly over multiple mass windows and thus acquires traces of multiple fragment ion masses

PIS used for qualitative applications to obtain structural information.
Q1 is set to allow only the transmission of one m/z. The parent ion collides with Argon gas in Q2 to create fragment or product ions. Product ions are scanned through Q3

All allow relative and absolute quantification of proteins, peptides and metabolites.