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Z705497 Sigma

Pitfalls and Errors of HPLC in Pictures, 2nd ed.

a practice-oriented guide for obtaining correct and reliable analytical results

  •  ISBN-10 3-52731372-9

  •  ISBN-13 978-3-52731372-3

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Related Categories Analytical/Chromatography, Applications, Books, Books and Software, Chromatography Books,
publication info   V. Meyer, John Wiley & Sons, 2006, 200 pp., soft cover
mfr. no.   Wiley

Description

General description

Every user of HPLC is confronted with a multitude of pitfalls and sources of error. Adding 12 new topics to this new, second edition, Veronika Meyer now offers almost 100 exemplary solutions for such problems. All examples are presented with a concise, instructive text and an informative figure.

These examples also include essential fundamentals as well as helpful strategies such as equipment tests or quality assurance strategies. A practice-oriented guide for obtaining correct and reliable analytical results.

Table of Contents

Part I: Fundamentals
1.1 Chromatography
1.2 Chromatographic Figures of Merit
1.3 The Resolution of Two Peaks
1.4 Reduced Parameters
1.5 The Van Deemter Curve
1.6 Peak Capacity and Number of Possible Peaks
1.7 Statistical Resolution Probability: Simulation
1.8 Statistical Resolution Probability: Example
1.9 Precision and Accuracy of an Analytical Result
1.10 Standard Deviation
1.11 Uncertainty Propagation
1.12 Reproducibility in Trace Analysis
1.13 Ruggedness
1.14 Calibration Curves
1.15 The HPLC Instrument
1.16 The Detector Response Curve
1.17 Noise
1.18 Causes and Effects Presented as an Ishikawa Diagram
1.19 The Possible and the Impossible

Part II: Pitfalls and Sources of Error

2.1 Mixing of the Mobile Phase
2.2 Mobile Phase pH
2.3 Adjustment of Mobile Phase pH
2.4 Inadequate Purity of a Mobile Phase Solvent
2.5 Inadequate Purity of a Mobile Phase Reagent
2.6 System Peaks and Quantitative Analysis
2.7 Sample Preparation with Solid Phase Extraction
2.8 Poor Choice of Sample Solvent: Peak Distortion
2.9 Poor Choice of Sample Solvent: Tailing
2.10 Sample Solvent and Calibration Curve
2.11 Impurities in the Sample
2.12 Formation of a By-Product in the Sample Solution
2.13 Decomposition by the Sample Vial
2.14 Artifact Peaks from the Vial Septum
2.15 Formation of an Associate in the Sample Solution
2.16 Precision and Accuracy with Loop Injection
2.17 Injection Technique
2.18 Injection of Air
2.19 Sample Adsorption in the Loop
2.20 Extra-Column Volumes
2.21 Dwell Volume
2.22 Elution at t0
2.23 Classification of C18 Reversed Phases
2.24 Different Selectivity of C18 Reversed Phases
2.25 Different Batches of Stationary Phase
2.26 Chemical Reaction within the Column
2.27 Recovery and Peak Shape Problems with Proteins
2.28 Double Peaks from Stable Conformers
2.29 Influence of Temperature on the Separation
2.30 Thermal Non-Equilibrium within the Column
2.31 Influence of the Volume Flow Rate on the Separation
2.32 Influence of Run Time and Volume Flow Rate on Gradient Separations
2.33 UV Spectra and Quantitative Analysis
2.34 UV Detection Wavelength
2.35 Fluorescence Quenching by Air
2.36 Detector Overload
2.37 Influence of the Retention Factor on Peak Height
2.38 Influence of the Volume Flow Rate on Peak Area
2.39 Leaks in the HPLC Instrument
2.40 Impairment of Precision as a Result of Noise
2.41 Determination of Peak Area and Height at High Noise
2.42 Peak Height Ratios
2.43 Incompletely Resolved Peaks
2.44 Area Rules for Incompletely Resolved Peaks
2.45 Areas for a 1 : 10 Peak Pair
2.46 Heights for a 1 : 10 Peak Pair
2.47 Quantitative Analysis of a Small Peak
2.48 Incompletely Resolved Peaks with Tailing
2.49
2.50
2.51
2.52

Part III:Useful Strategies.

3.1 Column Tests
3.2 Apparatus Tests
3.3 Wavelength Accuracy of the UV Detector
3.4 Internal Standards
3.5 A Linearity Test
3.6 Rules for Accurate Quantitative Peak Size Determination
3.7 High-Low Chromatography
3.8 Control Charts
3.9 Verification of the Analytical Result by Use of a Second Method
3.10 Description of Ruggedness
3.11 Rules for Passing On an HPLC Method
3.12
3.13
3.14
3.15
3.16
3.17
3.18
Index.

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