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A mixture of 14compounds was subjected to a reversed-phase gradient separation going from 5%to 100%acetonitrile with

a gradient time of 60min. The sample was injected at t =time. All peaks were eluted between 22and 50min.

(a) Is the mixture more suitable for isocratic or gradient elution?

(b) If the next run is a gradient, select the starting and ending %acetonitrile

and the gradient time.

Short Answer

Expert verified

The mixture is more suitable for gradient elution

Step by step solution

01

Define isocratic and gradient elution

isocratic elution refers to maintaining a constant concentration in the mobile phase, whereas gradient elution refers to maintaining a varying concentration in the mobile phase.

02

Calculating ∆ttG

First we need to calculatet:

t=50-22mint=28min

Then we calculatet/tG

role="math" localid="1663667217587" ttG=2860=0.47

Because the t/tG>0.40the mixture is more suitable for gradient solution.

Question: A mixture of \(14\) compounds was subjected to a reversed- phase gradient separation going from \(5\% \) to \(100\% \)acetonitrile with

a gradient time of \(60\)min. The sample was injected at \(t = \;dwell\;\) time. All peaks were eluted between \(22\)and\(50\)min.

(b) If the next run is a gradient, select the starting and ending % acetonitrile and the gradient time.

Answer:

The portions of the gradient from\(5{\rm{\;to\;}}40{\rm{\% }}\)acetonitrile and \(85{\rm{\;to\;}}100{\rm{\% }}\) acetonitrile were not needed. Therefore, the second run could be made with a gradient from \(40{\rm{\;to\;}}85{\rm{\% }}\) acetonitrile over the same \({t_G} = 60{\rm{min}}.\)

03

Define gradient time

tG the gradient time (the time from the start to the end of the gradient), VM the column hold-up volume and F the mobile phase flow rate. The gradient steepness parameter will vary with the S-value, which is only roughly constant for similar compounds.

04

The starting and ending of percentage acetonitrile and gradient time  

The next step in developing a gradient method is to spread the peaks out by choosing a shallower gradient. Peak 1 was eluted at 22 min when the solvent was 40% acetonitrile:

\(5 + \frac{{22}}{{60}} \cdot 95{\rm{\% }} = 40{\rm{\% }}\)

Peak \(2\) was eluted at \(50\)min, when the solvent was 85percent acetonitrile

\(5 + \frac{{50}}{{60}} \cdot 95{\rm{\% }} = 85{\rm{\% }}\)

The portions of the gradient from\(5{\rm{\;to\;}}40{\rm{\% }}\)acetonitrile and \(85{\rm{\;to\;}}100{\rm{\% }}\) acetonitrile were not needed. Therefore, the second run could be made with a gradient from \(40{\rm{\;to\;}}85{\rm{\% }}\) acetonitrile over the same \({t_G} = 60{\rm{min}}.\)

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Most popular questions from this chapter

The figure shows the separation of two enantiomers on a chiral stationary phase.


Sepation of enantiomers of Ritalin by HPLC with a chiral stationary phase.[Data from R.Bakhitar,L.Ramos,and F.L.S.Tse, “Quantification of methlylphenidate in plasma using chiral Liquid-chromatography/Tandem mass spectrometry: Application to Toxicokinetric studies,”Anal Chim Acta 2002,469,261.]

(a)From trandw1/2 find N for each peak.

(b) Fromtrandw1/2find the resolution.

(c)Giventm=1.62min, use Equation23-23with the average N to predict the resolution.

Retention factors for three solutes separated on aC8non-polar stationary phase are listed in the table. Eluent was a 70 : 30 (vol/vol) mixture of 50 mM citrate buffer (adjusted to pH withNH3) plus methanol. Draw the dominant species of each compound at each pH in the table and explain the behavior of the retention factors.

(a) You wish to use a wide gradient from 5 vol % to 95 vol %B for the first separation of a mixture of small molecules to decide whether to use gradient or isocratic elution. What should be the gradient time, tG,for a 15×0.46-cmcolumn containing 3-μmparticles with a flow of 1.0mL/min

You optimized the gradient separation going from 20vol%to 34 vol% Bin 11.5min at 1.0mLFindk*for this optimized

separation. To scale up to a 15×1.0cmcolumn, what should be the gradient time and the volume flow rate? If the sample load on

the small column was 1mgwhat sample load can be applied to the large column? Verify that k*is unchanged.

A bonded stationary phase for the separation of optical isomers has the structure

To resolve the enantiomers of amines, alcohols, or thiols, the compounds are first derivatized with a nitroaromatic group that increases their interaction with the bonded phase and makes them observable with a spectrophotometric detector.

When the mixture is eluted with 20 vol% 2-propanol in hexane, the (R)-enantiomer is eluted before the (S)-enantiomer, with the following chromatographic parameters:

Resolution=Δtrwav=7.7

Relative retention(α)=4.53

k for (R)-isomer =1.35

tm=1.00min

wherewavis the average width of the two Gaussian peaks at their base.

(a) Findt1,t2andwawith units of minutes.

(b) The width of a peak at half-height isrole="math" localid="1663582749865" w1/2(Figure 23-9). If the plate number for cach peak is the same, findw1/2for each peak.

(c) The area of a Gaussian peak is1.064×peakheight×w1/2. Given that the areas under the two bands should be equal, find the relative peak heights(heightR//heightS).

Question: Literature search problem: Human serum albumin (HSA) is an important protein ingredient in cryopreservation media used in procedures such as in vitro fertilization. Search the literature for a high-performance liquid chromatography method for the determination of human serum albumin and the stabilizer N-acetyl tryptophan in medical devices.

(a) Give the citation (authors, title, journal name, year, volume, pages) for the research paper that fits the criteria of this analysis.

(b) What alternative methods could be used for analysis of human serum albumin?

(c) What type of analytical column is used for the separation?

(d) How long was the gradient? How long were the additional wash and equilibration steps within the gradient method?

(e) What parameters were assessed in the method validation?

(f) Why were particles with 300 Å pores used?

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