/*! This file is auto-generated */ .wp-block-button__link{color:#fff;background-color:#32373c;border-radius:9999px;box-shadow:none;text-decoration:none;padding:calc(.667em + 2px) calc(1.333em + 2px);font-size:1.125em}.wp-block-file__button{background:#32373c;color:#fff;text-decoration:none} Q3 TY 25-3 What length of column packe... [FREE SOLUTION] | 91Ó°ÊÓ

91Ó°ÊÓ

25-3 What length of column packed with2μmparticles is needed to yield the same plate number as in Fugure 25.12? How long woald the separation take?

Short Answer

Expert verified

10 cm, on which separation would take only 10/25 or 40% as much time.

Step by step solution

01

Defining interpretation

Interpretation:

The length of the column that has to be packed with particles to have the same plate number has to be identified and the time taken for separation has to be calculated.

Concept Introduction:

Plate number is measure of peak dispersion on a HPLC column. This reflects the column performance. We can also find the efficiency of the column with this. Plate number can be calculated using the formula given below,

N≈3000)⋅1.(cm)dp(μm)

where

L is the length of column

dpis the size of the particles that is packed.

02

Finding length of column

The length of the column to be packed is 10cm and the time taken for the separation is only 40%.

The plate number (N) is given as 15000. The size of the particle that is packed in the column is given as .The length of the column that has to be taken to give the same plate number can be calculated using the formula

N≈3000⋅1.(cm)dp(mm)15000≈3000⋅L(cm)2(μmi)L(cm)=15000⋅23000=300003000=10cm

The length of the column is found to be 10 cm.

The time taken for separation using the 10 cm column instead of 25 cm column can be found by finding the ratio

1025×100=40%

Therefore, the separation using a 10cm column will take 40% as much time as using a 25cm column.

Unlock Step-by-Step Solutions & Ace Your Exams!

  • Full Textbook Solutions

    Get detailed explanations and key concepts

  • Unlimited Al creation

    Al flashcards, explanations, exams and more...

  • Ads-free access

    To over 500 millions flashcards

  • Money-back guarantee

    We refund you if you fail your exam.

Over 30 million students worldwide already upgrade their learning with 91Ó°ÊÓ!

One App. One Place for Learning.

All the tools & learning materials you need for study success - in one app.

Get started for free

Most popular questions from this chapter

After poisonous melamine and cyanuric acid appeared in milk in China (Box11-3) in 2008, there was a flurry of activity to develop methods to measure these substances. An analytical method for milk is to treat 1volume of milk with 9 volumes of H2O2CH3CN(20:80vol/vol)to precipitate proteins. The mixture is centrifuged for 5minto remove precipitate. The supernatant liquid is filtered through a 0.5-μ³¾filter and injected into a HILIC liquid chromatography column (TSK gel Amide-stationary phase) and products are measured by mass spectrometry with selected reaction monitoring (Section 22-5). Melamine is measured in positive ion mode with the transition³¾/³ú127→85. Cyanuric acid is measured in negative ion mode with the transition m/2128→42.

(a) Write the formulas for the four ions and propose structures for all four ions.

(b) Even though milk is a complex substance, only one clean peak is observed for melamine and one for cyanuric acid spiked into milk. Explain why

The rate at which heat is generated inside a chromatographycolumn from friction of flowing liquid is power (watts, W=J/s)= volume flow raterole="math" localid="1656474760665" (m3/s)×pressure drop (pascals, role="math" localid="1656474828044" Pa=kg/[m?s2]).

(a) Explain the analogy between heat generated in a chromatography column and heat generated in an electric circuit (power = current×voltage).

(b) At what rate (watts = J/s) is heat generated for a flow of 1 mL/minwith a pressure difference of3500 bar between the inlet and outlet?

You will need to convert mL/min tom3/s.Also 1 bar=105Pa.

what are criteria for an adequate isocratic chromatographic separation?

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)explain how to measure k and resolution.

(b)state three method for measuring tmin reversed-phase chromatography.

(c)state three method for measuring tmin hydrophilic interaction liquid chromatography.

(d)Estimate tmfor 15×0.46column containing 5-μ³¾particles operating at a flow rate of 1.5mL/minEstimate tmif the particle size were 3.5-μ³¾ instead.

See all solutions

Recommended explanations on Chemistry Textbooks

View all explanations

What do you think about this solution?

We value your feedback to improve our textbook solutions.

Study anywhere. Anytime. Across all devices.