Method conditions Excellent resolution and fast run times 2 x OligoPore, 4.6 x 250 mm columns gave excellent oligomeric resolution for the PS 580 sample.

Slides:



Advertisements
Similar presentations
Introduction to Chromatography
Advertisements

Gas Chromatography Introduction 1.) Gas Chromatography
Gas Chromatography There an be many parts to a gas chromatography system but the basic components include: An injection system. A column (controllable.
Foundation GPC Part 4 – Organic Gel Permeation Chromatography Columns and Applications.
Foundation GPC Training Course Theory. Nomenclature Gel Permeation ChromatographyGPC Size Exclusion ChromatographySEC Gel Filtration ChromatographyGFC.
1 HPLC Lecture Mobile Phase Selection in Partition Chromatography Optimization of the mobile phase composition and polarity is vital for obtaining.
HPLC 1. Introduction 1.Introduction CHROMATOGRAPHY Chromatography basically involves the separation of mixtures due to differences in the distribution.
1 1. Introduction H: High P : Performance (Pressure) L : Liquid C : Chromatography GC : Gas chromatography TLC: Thin layer chromatography IC : Ion chromatography.
Gradient Manipulation and 1.8 µm LC Columns for High Resolution Analysis of Herbal Supplements John W Henderson Jr, Thierry Faye, Ulrik Witteg, Maureen.
Introduction to Chromatographic Separations Due to lack of analytical specificity, separations are often necessary Chromatography is about separations.
Results Initial chromatographic conditions [Figure 2a caption] for the separation of the degradation products of aspirin were problematic due to the long.
Chapter 32 HIGH-PERRORMANCE LIQUID CHROMATOGRAPHY High-performance liquid chromatography (HPLC) is the most versatile and widely used type of elution chromatography.
The geometry of capillary columns is fairly simple, consisting of length, internal diameter, and stationary phase thickness. Nevertheless, there are endless.
Advanced GPC Part 1 – GPC and Viscometry
Column Chromatography. Types of columns: 1- Gravity Columns: The mobile phase move through the stationary phase by gravity force. 2- Flash Columns (Air.
High Performance Liquid Chromatography. HPLC originally refered to: High Pressure Liquid Chromatography currently refers to: High Precision Liquid Chromatography.
Gel Filtration Chromatography.
CHAPTER 29 Supercritical Fluid Chromatography The mobile phase is a supercritical fluid (a fluid above its critical T and critical pressure) Supercritical.
An Extended Range of Columns for Aqueous Size Exclusion Chromatography Greg Saunders, Graham Cleaver and Ben MacCreath, Varian, Inc., Church Stretton,
Chapter 6 - Chromatography
Introduction to High Performance Liquid Chromatography.
High Performance Liquid Chromatography
Chromatography Separates components in mixture: Based on - polarity
ADVANCED BIO-FRIENDLY POLYMERS Igor Lacík Gel permeation chromatography – a tool for determination of molar mass of polymers.
1.1 General description - Sample dissolved in and transported by a mobile phase - Some components in sample interact more strongly with stationary phase.
By: Thilag.k & Stephen. What is Hpcl??? Hplc or high performance liquid chromatography is the most widely used analytical separation technique. The difference.
Chapter 33 Supercritical-Fluid Chromatography
Varian 920-LC Integrated Analytical HPLC
Using Linear Scale-up Principles and the Varian 940-LC with Scale-Up Module for the Isolation of 5-Hydroxytryptophan from Griffonia Simplicifolia Dennis.
Simple Scale-up on a 940-LC Analytical to Preparative HPLC
History of Chromatography n Early LC carried out in glass columns n diameters: 1-5 cm n lengths: cm n Size of solid stationary phase n diameters:
Gihan Gawish.Dr High Performance Liquid Chromatography.
Chem. 230 – 9/23 Lecture.
INTRODUCTION TO CHROMATOGRAPY
CHROMATOGRAPHY Chromatography basically involves the separation of mixtures due to differences in the distribution coefficient.
Gas Chromatography Lecture 38.
HPLC – High Performance Liquid Chromatography
Chapter 29 Supercritical Fluid Chromatography and Extraction.
Simulation of gel permeation (size exclusion) chromatography Jetse Reijenga 1, Wieb Kingma 1, Dušan Berek 2, Milan Hutta 3 1 Eindhoven University of Technology.
1 Gas Chromatography Lecture Liquid Stationary Phases In general, the polarity of the stationary phase should match that of the sample constituents.
Introduction to Chromatography. Introduction Chromatography permit the scientist to separate closely related components of complex mixtures. In all chromatographic.
The Chromatogram  Terms:  Retention time  Peak area  Peak width (at half height, at base)  Peak height  Void time/volume  Adjusted retention time.
Created with MindGenius Business 2005® Instrumentation (1) Instrumentation (1) Origins Preparative column chromatography (Glass columns) Internal diameter:
Chromatography High Performance Liquid Chromatography HPLC Chapter Dr Gihan Gawish.
HPLC.
Chapter 28 High Performance Liquid Chromatography.
LC/MS Chromatography Systems 212-LC. 2 The Complete Solution Varian LC components, pumps, autosamplers and the New MS Workstation SW (V6.6) can be used.
Liquid Chromatography 2: New Technology Lecture Date: April 3 rd, 2007.
Selling Restek LC Solutions for Analytical Scale Laboratories Rick Lake Product Line Manager Liquid Chromatography x 2379
Lecture 10 ANALYTICAL METHOD DEVELOPMENT AND VALIDATION IN HPLC AND GC. Lecture 10 – Chromatography, Dr. Rasha Hanafi 1© Dr. Rasha Hanafi, GUC.
Instrumental Analysis (I) HPLC Tutorial 8. Graded presentation Students in groups of 4-5 individuals are asked to prepare a presentation (weight=5% of.
Instrumental Analysis (I)  HPLC Tutorial #7 PHCMt561 – 5 th Sem. Pharm.
Maggi Tebrake– Early Pharmaceutics & Technology, 3M Health Care Ltd, Loughborough Lindsey Gunby– Industrial Placement Student (EP&T ), 3M Health.
PREPARED BY VAISHNANI BHAVIN M.PHARMA-I (Q.A.). Qualitative error sources in HPLC: Poor separation power. Some special substances from the samples can.
Evolution GC-MS/MS: Pesticide analysis in canola oil Evolution GC-MS/MS: Pesticide analysis in canola oil Vivian Watts 1, Ingo Christ 1, Mark Misunis 2.
Experiments in Analytical Chemistry
1.1 General description - Sample dissolved in and transported by a mobile phase - Some components in sample interact more strongly with stationary phase.
Laboratory class on next Wednesday
High Performance Liquid Chromatography Presented by Dr. Kamal Modi 2 nd Year Resident.
Gel Permeation Chromatography Size Exclusion Chromatography
Chem. 133 – 5/9 Lecture.
Chem. 133 – 5/11 Lecture.
Size Exclusion Chromatography (SEC)
Gel Filtration Chromatography.
BASICS OF SUPERCRITICAL FLUID CHROMATOGRAPHY
Chromatography Daheeya Alenazi.
Principle of separation of different components:
High-Performance Liquid Chromatography
High performance liquid chromatography (HPLC)
High-Performance Liquid Chromatography
Presentation transcript:

Method conditions Excellent resolution and fast run times 2 x OligoPore, 4.6 x 250 mm columns gave excellent oligomeric resolution for the PS 580 sample. Resolution was largely maintained at the 1.2 mL/min flow rate, where run time was less than 6 minutes. Figure 1: PS 580 run on 2 x OligoPore, 4.6 x 250 mm, columns at 0.3 (bottom trace), 0.6 (middle trace), and 1.2 mL/min (top trace). Normalized retention time. 2 x MesoPore 4.6 x 250 mm, columns gave excellent resolution for the oligomers in epoxy resin samples. Some exclusion was observed for higher molecular weights. Figure 2: Epikote 1004 (bottom trace), 1007 (middle trace) and 1009 (top trace) run on 2 x MesoPore, 4.6 x 250 mm, columns at 0.3 mL/min. Again, this resolution was largely maintained at the highest flow rate – and run time of less than 6 minutes. Figure 3: Epikote 1004 run on 2 x MesoPore, 4.6 x 250 mm, columns at 1.2 mL/min. Additional reduction in solvent consumption The lower flow rate required for GPC/SEC columns with an internal diameter of 4.6 mm gives a 70% saving in solvent consumption compared to 7.5 mm id. If the column internal diameter is reduced to 2.1 mm this saving becomes 94%. As is the case with UHPLC, using 2.1 mm id columns careful control of system dispersion, which includes the detector flow cell volume, is critical. Resolution was achieved with 2 x MesoPore, 2.1 x 250 mm, columns at all flow rates. This resolution could be improved by further reduction of system dispersion volume. Figure 4: Epikote 1004 run on 2 x MesoPore 2.1 x 250 mm, columns at 0.06 (bottom trace), 0.12 (middle trace), and 0.24 mL/min (top trace). Normalized run time. Investigating Miniaturization in GPC/SEC Stephen Luke, Peter Cooke, and Graham Cleaver EN Agilent Technologies, UK Introduction Conclusions Experimental Results and Discussion 2015 ParameterChangeBenefitConsideration Flow rateLower Decreased solvent consumption Pump flow rate precision Peak volumeLower Increased sensitivity System dispersion volume Peak widthNarrowerHigher resolution Detector data (sampling) rate SampleColumns PS x Agilent OligoPore, 4.6 x 250 mm Linear MW range up to 3,300 g/mol SampleColumns Epikote 1004 Epikote 1007 Epikote x Agilent MesoPore, 4.6 x 250 mm Linear MW range up to 25,000 g/mol Column Set0.3 mL/min0.6 mL/min1.2 mL/min 2 x OligoPore, 4.6 x 250 mm28 bar56 bar112 bar 2 x MesoPore, 4.6 x 250 mm41 bar82 bar170 bar Column Set0.06 mL/min0.12 mL/min0.24 mL/min 2 x OligoPore, 2.1 x 250 mm21 bar42 bar84 bar 2 x MesoPore, 2.1 x 250 mm30 bar20 bar125 bar Experimental Column:4.6 x 250 mm2.1 x 250 mm Run Time Mobile phase:THF Flow rate: 0.3 mL/min 0.6 mL/min 1.2 mL/min 0.06 mL/min 0.12 mL/min 0.24 mL/min 24 minutes 12 minutes 6 minutes Sample conc.:1 mg/mL Inj. volume:2 μL0.5 μL Temperature: 50 °C SampleColumns PS x Agilent OligoPore, 2.1 x 250 mm Linear MW range up to 3,300 g/mol SampleColumns Epikote x Agilent MesoPore, 2.1 x 250 mm Linear MW range up to 25,000 g/mol GPC/SEC is an important liquid chromatographic technique for determining the molecular weight distribution and averages of a polymer and for comparing batch-to-batch polymer quality. Miniaturization, the use of smaller column dimensions, has been a popular approach in many liquid chromatographic techniques. The benefits of miniaturization include reduced solvent costs, higher throughput, increased detector response, and taking full advantage of the latest advances in liquid chromatography instrument design. In this work we investigate how miniaturization can be applied to gel permeation chromatography, discuss critical considerations, and determine what benefits the approach brings for size based separations. Miniaturization Conventional analytical-scale GPC/SEC separations are performed using columns with a length of 300 mm and internal diameter between 7.5 and 8.0 mm. Optimum linear velocities in GPC are relatively low and as a result flow rates of 1.0 mL/min are used. To achieve acceptable resolution, multiple columns are often connected in series leading to typical run times of 45 to 60-minutes per analysis with solvent consumption of up to 60 mL. The impact of GPC/SEC miniaturization is summarized below. GPC/SEC columns with a length of 250 mm and an internal diameter of 4.6 mm, for example PLgel MiniMIX, have been available for some time. This work investigates what is now possible with high performance GPC/SEC columns, new column formats, and the latest advances in liquid chromatography instrument design. GPC/SEC instruments An Agilent 1260 Infinity GPC/SEC system with 1290 Infinity II µRID was used. The Agilent 1260 Infinity Isocratic Pump features virtually pulse-free and stable solvent flow, making it the ideal pump for GPC/SEC applications where run-to-run and day-to-day precision of retention times is important. The 1290 Infinity II µRID is optimized for use with fast separations on narrow internal diameter columns, optimized fluidic connections, 2.1 µL flow cell volume, and a maximum data rate of 148 Hz. Data were collected and processed using Agilent GPC/SEC software version 1.2. High performance GPC/SEC columns High performance columns that deliver significantly increased resolution compared to a conventional GPC/SEC column set allow the use of fewer columns in series and higher linear velocities, without sacrificing separation quality. To clearly demonstrate the performance of miniaturization we used polystyrene and epoxy resin samples with columns that would resolve numerous oligomer peaks. Further miniaturization and faster separations We also investigated the use of further miniaturization with even narrower internal diameter columns. To investigate how fast miniaturized GPC/SEC separations can be, each sample was run at three different flow rates; from the normal linear velocity (equivalent to 1.0 mL/minute on a 7.5 mm id column) to 4x this flow. Reproducible and reliable results Reproducible retention times are critical for accurate and reliable GPC/SEC. 2 x MesoPore 2.1 x 250 mm, columns show retention time precision of 0.04% RSD even at the lowest flow rate of 0.06 mL/min. Figure 5: PS 580 run six times on 2 x OligoPore, 2.1 x 250 mm, columns at 0.06 mL/min. The PS/DVB particles packed in OligoPore and MesoPore high performance columns are a proven technology for GPC/SEC, meaning that methods can be transferred with confidence without the risk of absorbance effects or other interactions between the analytes and stationary phase. High pressure rating not required As discussed, GPC/SEC miniaturization does require the careful control of system dispersion volume that is a feature of UHPLC instruments. However, it does not require the very high pressures that these instruments are designed to support. Pressures generated by the different column/flow rate combinations were all well within the 600 bar pressure limit of the Agilent 1260 Infinity GPC/SEC system. Table 1: Pressures at each column/flow rate combination In combination with a low volume detector flow cell and high detector data rate, miniaturized high performance GPC/SEC columns are capable of generating excellent resolution and fast run times. Miniaturization to high performance GPC/SEC columns with a 2.1 mm internal diameter allows solvent consumption to be reduced by 94% compared to 7.5 mm columns. Providing high precision solvent delivery is available at low flow rates, highly reproducible results can be obtained with miniaturized high performance GPC/SEC columns. Miniaturized high performance GPC/SEC columns packed with proven PS/DVB particles do not require very high pressure to operate even at elevated flow rates and thus, provided that other dependencies discussed are met, can be used on existing instruments.