final exam 2 stuff Flashcards

1
Q

whats the difference between capillary and packed column GC’s

A

capillary columns are long and thin and have a stationary “waxy” coating on the inside

packed columns have “balls” of stationary phase

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1
Q

what’s the differen

A
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2
Q

how do we adjust the retention in a GC?

A

we can adjust the temperature, the flow rate, and the chemical nature of the stationary phase

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3
Q

what does adjusting the temperature do to a GC?

A

if we heat the colum, it will cause less retention since more of the molecules will be in the gaseous phase

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4
Q

how do we adjust the chemical nature of the stationary phase

A

we can make it more polar or nonpolar

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5
Q

how do we generally adjust the retention of analytes in LC and GC

A

it’s easier to adjust the mobile phase rather than the stationary phase

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6
Q

what affects the retention in gas chromatography

A

a combination of the boiling point and the polarity

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7
Q

how does the boiling point play into gas chromatography

A

analytes with low boiling points are more volatile and will go into the mobile phase easier

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8
Q

in GC, the separation is based on the difference in partitioning between:

A

the stationary and gas (mobile phase)

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9
Q

When we increase the column temperature, what happens to the gas phase concentration? To what solutes?

A

The gas phase concentration of ALL solutes increases with increased temperatures

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10
Q

why is it a problem when we increase the temperature?

A

all the analytes are affected and may not be completely resolved

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11
Q

why is it a problem when we decrease the temperature

A

it is inefficient we get better resolution and separation but the peaks become broader and it takes more time

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12
Q

what is temperature programmed chromatography?

A

it is where we increase the temperature of the column during a run

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13
Q

when we don’t use temperature programmed chromatography what happens when we get resolution with early eluters

A

the late eluters get too broad or do not elute

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14
Q

when we don’t use temperature programmed chromatography what happens when we get resolution/narrow peaks with late eluters?

A

the early eluters do not get resolved

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15
Q

what is a gradient in liquid chromatography

A

it is when we alter the composition of the mobile phase during the run in order to achieve better separation in less amounts of time

16
Q

what is the difference in mobile phases for HPLC and GC

A

in GC we have a gas mobile phase

in HPLC we have a liquid mobile phase

17
Q

is HPLC isothermal?

A

yes, it is difficult to change the temperature

18
Q

is GC isothermal

A

no, we often change the temperature to change the mobile phase

19
Q

in a GC, how do the analytes interact with the mobile and stationary phases

A

the analyte interacts with the stationary phase only, the mobile phase serves as a carrier

20
Q

in a HPLC, how do the analytes interact with the mobile and stationary phases?

A

the analytes interact with both the mobile and stationary phases

21
Q

if we make the mobile phase and stationary phases in a HPLC more similar what happens to the retention times?

A

the times decrease

22
Q

if we make the mobile phase and stationary phase in a HPLC less similar, what happens to the retention times?

A

the times increase

23
Q

what are the best analytes for LC

A

analytes that are non-volatile

24
Q

what are the best analytes for GC

A

analytes that are volatile

25
Q

why do we not use normal phase HPLC very often?

A

normal phase HPLC has a nonpolar mobile phase,

usually nonpolar analytes are more volatile and can be used more easily in a GC separation