spectroscopy 2 Flashcards

1
Q

what are the two types of atomic spectroscopy?

A

1- atomic emission

2- atomic absorption

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2
Q

if your energy is in the form of a radio wave what spectroscopy do you have?

A

atomic absorption spectra

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3
Q

if your energy is in the form of a flame what type of spectroscopy do you have?

A

flame emission spectra

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4
Q

what group in the periodic table is emission best for?

A

group 1- mostly bodily fluids eg lithium

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5
Q

what group is absorption better for?

A

higher group elements

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6
Q

what does the intensity of the light depend on?

A

number of atoms in the excited state

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7
Q

what kind of light is emitted from the flame?

A

propane think bandwith

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8
Q

what are the two limitations associated with the spectra?

A

1- self absorption- has to be linear and at higher conc. iit is not linear
2-excitation source- flame is not a homogeneous temp

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9
Q

what is the hollow cathode lamp?

A

glass tube filled with inert gas with the element to be analysed
positive ions are accelaterated towards the cathode
metal atoms are in gas phase

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10
Q

what is absorption defined as?

A

A = -log T = -log I/I0= a x b x c

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11
Q

what law does absorption follow?

A

beer lambert law ( linear)

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12
Q

what are limitations of the hollow cathode lamp?

A
  • must have a large volume
  • sensitive detection
  • not possible to analyse solid samples
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13
Q

what are the 3 types of interferences in AA?

A

chemical
ionisation
spectracal

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14
Q

how does chemical interfere with AA?

A

molecule must be thermo stable complex with ionically stable species
if not releasing agent must be added

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15
Q

how does ionisation affect AA?

A

Alkali and alkaline earth metals have low ionization potential
so addition of ionisation suppressor ( something that ionises easier)

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16
Q

how does spectral affect AA?

A

can be overlap of spectrums

17
Q

what happens to the graph if the standard mixes with the matrix?

A

not as full of a reaction- line not as steep

18
Q

how do you interfere with the matrix?

A

add standard to different samples and plot till you get a line of best fit, where it cuts the X axis is the original amount of sample in solution