(a) What types of solutes are typically separated with a poly(dimethylsiloxane)-coated open tubular column?

(b) What types of solutes are typically separated with a poly(ethylene glycol)-coated open tubular column?

(c) What types of solutes are typically separated with a porous-layer open tubular column?

Short Answer

Expert verified

(a.)

Selecting a liquid stationary phase depends on the rule "like dissolves like". This signifies that the Polarity of the column must be the same as that of the solute

(b.) Solutes that are typically separated with a poly(dimethylsiloxane)-coated open tubular column are the following (based on Table 24-1)

(c.) Porous-layer columns contain porous solid particles with large surface area that adhere to the column wall. The highly retentive surface of the particles serve as the active stationary phase. Solutes that are typically separated with a porous-layer open tubular column areHe,Ar2O2,N2,CH4andCO. Furthermore, porous polymers, high-surface-area carbon , and alumina (Al2O3)can separate hydrocarbons in gas-solid adsorption chromatography.

Step by step solution

01

To find the types of solutes are typically separated with a poly(dimethylsiloxane)-coated open tubular column 

(a)

Selecting a liquid stationary phase depends on the rule "like dissolves like". This signifies that the Polarity of the column must be the same as that of the solute

02

find the types of solutes are typically separated with a poly(ethylene glycol)-coated open tubular column

03

Step 3: types of solutes are typically separated with a porous-layer open tubular column

(C)

Porous-layer columns contain porous solid particles with large surface area that adhere to the column wall. The highly retentive surface of the particles serve as the active stationary phase. Solutes that are typically separated with a porous-layer open tubular column areHe,Ar2O2,N2,CH4andCO. Furthermore, porous polymers, high-surface-area carbon , and alumina (Al2O3)can separate hydrocarbons in gas-solid adsorption chromatography.

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Most popular questions from this chapter

The graph shows van Deemter curves for n-nonane at . in the 3.0-m-long microfabricated column in Box 24-2 with a -thick stationary phase.

van Deemter curves. [Data from G. Lambertus, A. Elstro, K. Sensenig, J. Potkay, M. Agah, S. Scheuening, K. Wise, F. Dorman, and R. Sacks, "Design, Fabrication, and Evaluation of Microfabricated Columns for Gas Chromatography," Anal. Chem. 2004, 76, 2629.]

(a) Why would air be chosen as the carrier gas? What is the danger of using

air as carrier gas?

(b) Measure the optimum velocity and plate height for air and for carrier

gases.

(c) How many plates are there in the 3 -m-long column for each carrier gas at

optimum flow rate?

(d) How long does unretained gas take to travel through the column at

optimum velocity for each carrier gas?

(e) If stationary phase is sufficiently thin with respect to column diameter, which of the two mass transfer terms (23-40 or 23-41) becomes negligible?

Why?

(f) Why is the loss of column efficiency at high flow rates less severe for

than for air carrier gas?

(a) If retention times are 1.0 min for CH4, 12.0 min for octane, 13.0 min for unknown, and 15.0 min for nonane, find the Kovats retention index for the unknown. (b) What would be the Kovats index for the unknown if the phase ratio of the column were doubled? (c) What would be the Kovats index for the unknown if the length of the column were halved

(a) How can you improve the resolution between two closely spaced peaks in gas chromatography?

(b) What approach from (a) would be most cost effective (not involve a purchase)?

(a) Write the meaning of the retention factor, , in terms of time spent by solute in each phase. (b) Write an expression in terms of for the fraction of time spent by a solute molecule in the mobile phase. (c) The retention ratio in chromatography is defined as

R=timeforsolventtimeforsolutetopassthroughcolumn=tmtrShow that is related to the retention factor by the equationR=1/k+1

State the order of decisions in method development for gas chromatography.

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