VGA-100 Instrument Detection Limits and Linearity

Similar documents
We don t have anything against mass spectrometry. We just think it s time for a worthy alternative.

The Analysis of Residual Solvents in Pharmaceutical Products Using GC-VUV and Static Headspace

VUV ANALYTICS VGA-100 GC DETECTOR Gas Chromatograph Agilent 6890 equipped with a 7683 model autosampler Restek 30m x 0.25mm x 0.

Characterisation of allergens in cosmetics by GC GC TOF MS with Select-eV variable-energy electron ionisation

Automated PIONA Analysis by ASTM D8071 and VUV PIONA+

Permanent Gas Analysis by Gas Chromatography Vacuum Ultraviolet Spectroscopy

We don t have anything against mass spectrometry. We just think it s time for a worthy alternative.

Characterisation of allergens in cosmetics by GC GC TOF MS with Select-eV variable-energy electron ionisation

Optimizing GC Parameters for Faster Separations with Conventional Instrumentation

Analysis of Biomarkers in Crude Oil Using the Agilent 7200 GC/Q-TOF

UNIQUE SOLUTION FOR FLAVOUR AND FRAGRANCE IDENTIFICATION BY MEANS OF GC-MS (TOF) / CONDENSED PHASE FTIR

HIGH SPEED GC-TOFMS FOR ESSENTIAL OILS PROFILING IN ROUTINE QUALITY ASSESSMENT

Analysis of allergens found in cosmetics using MDGC-GCMS (Multi-Dimensional Gas Chromatograph Mass Spectrometer)

Multi-residue Analysis for PAHs, PCBs and OCPs on Agilent J&W FactorFour VF-Xms

Spring 2010 updated March 24 Determination of Aromatics in Gasoline by Gas Chromatography- Mass Spectrometry: Comparison of Grades and Brands

Jack Cochran, Lindsey Shear-Laude, Alex Hodgson VUV Analytics Emerald Conference. #emeraldconference

Characterization of petroleum samples via thermal analysis coupled to APCI FTMS

Analysis of Terpenes in Cannabis Using the Agilent 7697A/7890B/5977B Headspace GC-MSD System

Residual Solvents in Pharmaceuticals by USP Chapter <467> Methodology

AppNote 7/2003. Coupling Retention Time Locked Methods and Libraries to Automated SPME or SBSE for Analysis of Flavors and Fragrances

Practical Faster GC Applications with High-Efficiency GC Columns and Method Translation Software

Chlorinated Compounds in Hydrocarbon Streams Using a Halogen Specific Detector (XSD)

AppNote 7/2003. Coupling Retention Time Locked Methods and Libraries to Automated SPME or SBSE for Analysis of Flavors and Fragrances KEYWORDS

Rely on Rxi -PAH Columns

This document is a preview generated by EVS

Ultrafast and sensitive analysis of sweeteners, preservatives and flavorants in nonalcoholic beverages using the Agilent 1290 Infinity LC system

Determination of 59 potential Allergens in Perfumes by twin-line fast GCMSMS

Applying the Technology of the TurboMatrix 650 ATD to the Analysis of Liquid Accelerants in Arson Investigation

U.S. EPA Method 8270 for multicomponent analyte determination

Simultaneous Compound Identification and Quantification with Parallel Polyarc /FID and MS

Separation and Characterization of Indian and Australian Sandalwood Oils

Application Note # Performance of Method 8270 Using Hydrogen Carrier Gas on SCION Bruker SCION GC-MS

GC Application Note. Dilution/standard addition: Efficient and traceable.

Sensitive and rapid determination of polycyclic aromatic hydrocarbons in tap water

A Newly Approved ASTM Standard For Analysis of Thiophene in Benzene Using a Pulsed Flame Photometric Detector (PFPD)

Determination of VOC in Artificial Runway by Multiple Headspace Extraction-GC/MS. Gas Chromatography/ Mass Spectrometry APPLICATION.

Analysis of Trace (mg/kg) Thiophene in Benzene Using Two-Dimensional Gas Chromatography and Flame Ionization Detection Application

Achieve confident synthesis control with the Thermo Scientific ISQ EC single quadrupole mass spectrometer

Application Note S/SL

Hydrogen as a Carrier Gas in the Analysis of Polar/Non-Polar Compounds Using the Polyarc System. Application Note. Author. Introduction.

Expectations for GC-MS Lab

GAS CHROMATOGRAPHY MASS SPECTROMETRY. Pre-Lab Questions

A Fast, Simple FET Headspace GC-FID Technique for Determining Residual Solvents in Cannabis Concentrates

A New PEG GC Column with Improved Inertness Reliability and Column Lifetime Agilent J&W DB-WAX Ultra Inert Polyethylene Glycol Column

Chromatography & instrumentation in Organic Chemistry

This project has been funded with support from the European Commission. This publication reflects the views only of the authors, and the Commission

The GC-APCI Interface for the Agilent Q-TOF LC/MS System Improves Sensitivity, Mass Accuracy, and Speed for a Wide Range of GC Applications

Determination of Hydrocarbon Components in Petroleum Naphthas

Quantification of Pesticides in Food without Calibration using GC/FID with the Polyarc Reactor

Discovering the Scent of Celery: HS-SPME, GC-TOFMS, and Retention Indices for the Characterization of Volatiles

Katherine K. Stenerson, Michael Ye, Michael Halpenny, Olga Shimelis, and Leonard M. Sidisky. Supelco, Div. of Sigma-Aldrich Bellefonte, PA USA

Enhanced Simultaneous Total ion and Selective Multi-Ion GC/MS Using a Combination of New Software and Low-Bleed Columns

The Use of Tandem Quadrupole GC/MS/MS for the Determination of Polycyclic Aromatics Hydrocarbons (PAHs) in Food Products

Accelerated Solvent Extraction GC-MS Analysis and Detection of Polycyclic Aromatic Hydrocarbons in Soil

APPLICATION NOTE. A Capillary Approach to ASTM D3606: Test Method for Determination of Benzene and Toluene in Finished Motor and Aviation Gasoline

Application Note. Agilent Application Solution Analysis of PAHs in soil according to EPA 8310 method with UV and fluorescence detection.

A Fast, Simple FET Headspace GC-FID Technique for Determining Residual Solvents in Cannabis Concentrates

The Use of the ACQUITY QDa Detector for a Selective, Sensitive, and Robust Quantitative Method for a Potential Genotoxic Impurity

Chromatographic Methods of Analysis Section: 5 Gas Chromatography (GC) Prof. Tarek A. Fayed

Practical Faster GC Applications with High-Efficiency GC Columns and Method Translation Software

Reprinted from February Hydrocarbon

Analysis of Sulfur-Containing Flavor Compounds By GC/MS With A PFPD

Selection of a Capillary

Virtually Particle-Free Rt -Silica BOND Columns

Appendix 1: Polycyclic Aromatic Compounds: Nomenclature and Analysis

Fast Determination of Impurities in Propane- Propylene Streams Using a Pulsed Flame Photometric Detector (PFPD) and a New Capillary.

UNDERSTANDING SOIL TPH RESULTS Peter Robinson, Hill Laboratories, Hamilton, NZ

Application Note. Abstract. Introduction. Determination of Polycyclic Aromatic Hydrocarbons in Seafood by an Automated QuEChERS Solution

New ZB-5HT Inferno The World s Highest Temperature Non-Metal GC Column

Rapid Analysis of Food and Fragrances Using High-Efficiency Capillary GC Columns. Application. Authors. Abstract. Introduction

Application Note. Authors. Abstract. Energy & Chemicals, Biofuels & Alternative Energy

Application Note. Author. Abstract. Introduction. Hydrocarbon Processing

Analysis of Bakken Oil Samples

Liquid storage: Holds the solvent which is going to act as the mobile phase. Pump: Pushes the solvent through to the column at high pressure.

Quantification of Rice Aroma, 2-Acetyl-1-Pyrroline (2-AP), Using TurboMatrix Headspace Trap Coupled with GC/NPD and GC/MS

Case 1:13-cv WBH Document Filed 12/30/16 Page 406 of 519. Exhibit 53

UNIT 3 CHEMISTRY. Fundamental Principles in Chemistry

Fast, Quantitative Analysis of Residual Solvents in Cannabis Concentrates

Defense Technical Information Center Compilation Part Notice

Take Your Food Testing to the Next Level

Author. Abstract. Introduction

Developing Large Volume Injection (LVI) in Split / Splitless Inlets. Philip J. Koerner Phenomenex Inc. NEMC 2014

SERVOTOUGH SpectraScan

PAH Analyses with High Efficiency GC Columns: Column Selection and Best Practices

ENVIRONMENTAL analysis

Quantification of growth promoters olaquindox and carbadox in animal feedstuff with the Agilent 1260 Infinity Binary LC system with UV detection

Characterisation of the Aerosol Collection Module (ACM) Dagmar Trimborn, John Jayne, Thorsten Hohaus

Selection of a Capillary GC Column

Determination of 24 PAHs in Drinking Water

Fast and Accurate Analysis of PBDEs in a Single Run, Including BDE-209

Analysis of Polyphenols in Saffron Petal Extracts with UHPLC/UV/MS

Analysis of Ethanol and Isotopomers by 240 Quadrupole Ion Trap GC/MS

SEAMLESS INTEGRATION OF MASS DETECTION INTO THE UV CHROMATOGRAPHIC WORKFLOW

Fast and Accurate Analysis of PBDEs in a Single Run, Including

is given for the isotopic fingerprinting methodology.

Analyzing Residual Solvents in Pharmaceutical Products Using GC Headspace with Valve-and-Loop Sampling

STANDARD OPERATING PROCEDURES SOP: 1828 PAGE: 1 of 14 REV: 0.0 DATE: 05/12/95 ANALYSIS OF METHYL PARATHION IN CARPET SAMPLES BY GC/MS

Introduction to GC/MS

CALIBRATION OF GC/MS METHOD AND VALIDATION OF THE MODIFIED SAMPLE PREPARATION FOR DETERMINATION OF POLYCYCLIC AROMATIC HYDROCARBONS

Transcription:

VGA-100 Instrument Detection Limits and Linearity The VGA-100 is the world s first benchtop vacuum ultraviolet (VUV) spectrometer for gas chromatography (GC). It is a universal GC detector that provides both qualitative and quantitative data. The strong absorption of gas phase molecules in the VUV region of the ultraviolet spectrum (120 240 nm) provide excellent sensitivity, and the compound-specific absorption spectra provide unparalleled selectivity. VUV spectroscopy follows first principles detection and provides a predictable linear response that eliminates the need for continuous calibration. Analyte concentration can be easily determined by the Beer-Lambert Law used commonly in UV-VIS spectroscopy applications. Demonstrated Instrument Performance Quantitative analysis of compounds important to many industries including food & beverage, flavors & fragrances, petrochemical, and fuel refining was performed using the VGA-100 Gas Chromatography (GC) detector. Instrument detection limit (IDL) and linearity measurements of these compounds used a concentration range of 20 pg-50 ng. The VGA-100 IDLs averaged between 20-60 picograms (pg) on column with excellent linearity across three orders of magnitude.

Experimental Conditions The following concentrations, sample replicates, GC settings, and data processing conditions were used unless otherwise noted. Instrument detection limit (IDL) and linearity measurements were taken across a concentration range of 20 pg-50 ng. Detection limits were calculated based upon a determination of the statistical variance in eleven replicate measurements at a low but detectable amount on column. A spectral filter of 140 160 nm was applied post-data acquisition to optimize for signal to noise. VGA 100 Data acquisition rate: 4.5Hz GC Oven: 70 o C, hold 0.1 minutes; ramp at 20 o C/min to 330 o C, hold until last compound elutes GC Injection volume: 1µl, 275 o C Split injections, 4mm Precision split liner with wool Paraffins Paraffins are used in a variety of consumer products and separated in oil refineries by fractional distillation. This study measured n-decane, n-eicosane, n-triacontane, and n-tetracontane at concentrations between 50 pg-50 ng on column. Paraffin IDLs averaged 41 pg on column with an R 2 of 0.9945. Experimental A Restek certified reference material (Catalog # 31266) was used in the experiment. Detection limits were calculated based upon a determination of the statistical variance in ten replicate measurements at a low but detectable amount on column. Figure 1: n-decane, n-eicosane, n-triacontane, and n-tetracontane IDL linearity data results from measurement with a VGA-100

Figure 2: n-decane linearity plot showing VGA-100 measurement performance from 50 pg-50 ng on column Polycyclic Aromatic Hydrocarbons Polycyclic Aromatic Hydrocarbons (PAH) are ubiquitous, toxic compounds comprised of multiple aromatic rings. They commonly result from the incomplete combustion of organic matter and transformation of organic sediments into fossil fuels. This study measured Acenaphthylene, Fluorene, Benzo[a]pyrene, and Benzo[g,h,i]perylene at concentrations between 20 pg-20 ng and 20 pg-50 ng on column. PAH IDLs averaged 28 pg on column with an R 2 of 0.9936. Experimental A Restek certified reference material (Catalog # 31011) was used in the experiment. Detection limits were calculated based upon a determination of the statistical variance in twelve replicate measurements at a low but detectable amount on column. A spectral filter of 170 240 nm was applied post-data acquisition to optimize for signal to noise. Figure 3: Acenaphthylene, Fluorene, Benzo[a]pyrene, and Benzo[g,h,i]perylene IDL and linearity data results from measurement with a VGA-100

Figure 4: Fluorene linearity plot showing VGA-100 measurement performance from 20 pg-50 ng on column Terpenes Terpenes are commonly found in conifer plants and are key ingredients in flavor, fragrance, and alternative medicine applications. This experiment measured alpha- Pinene, gamma-terpinene, Geraniol, and alpha-bisabolol. Terpene IDLs averaged 28 pg on column with an R 2 of 0.9971. Experimental A Restek certified reference material (Catalog # 34095) was used in the experiment. GC Oven: 40 o C, hold 0.1 minutes; ramp at 15 o C/min to 250 o C, hold until last compound elutes Figure 5: alpha-pinene, gamma-terpinene, Geraniol, and alpha-bisabolol linearity data results from measurement with a VGA-100

Figure 6: alpha-pinene linearity plot showing VGA- 100 measurement performance from 20 pg-50 ng on column FAMEs Fatty acids and their corresponding methyl esters (FAMEs) are important analytes for consideration in terms of food science, nutrition, and bio-based fuels. This experiment measured Methyl Decanoate, Methyl Laurate, Geraniol, Methyl Palmitate, and Methyl Docosanoate at concentrations between 20 pg-50 ng and 50 pg-50 ng on column. FAME IDLs averaged 34 pg on column with an R 2 of 0.9940. Experimental A Sigma Aldrich certified reference material (Catalog # 49453-U) was used in the experiment. GC Oven: 70 o C, hold 0.1 minutes; ramp at 20 o C/min to 300 o C, hold until last compound elutes Figure 7: Methyl Decanoate, Methyl Laurate, Methyl Palmitate, and Methyl Docosanoate linearity data results from measurement with a VGA-100

Figure 8: Methyl Decanoate linearity plot showing VGA-100 measurement performance from 20 pg-50 ng on column Fragrance Allergens Cosmetic products are typically required to label fragrance compounds having concentrations exceeding 100 ppm. This study measured standard mixtures Fragrance Allergen [A], [B], and [C] from Restek at concentrations between 20 pg-20 ng on column. Fragrance allergen [A], [B], and [C] IDLs averaged 35, 44, and 36 pg on column with R 2 of 0.9938, 0.9952, 0.9910, respectively. Fragrance Allergen [A] Experimental A Restek certified reference material (Catalog # 33102) was used in the experiment. Figure 9: Phenylacetaldehyde, Lilial, alpha-amylcinnamaldehyde, and alpha- Hexylcinnamaldehyde linearity data results from measurement with VGA-100

Figure 10: Phenylacetaldehyde linearity plot showing VGA-100 measurement performance from 20 pg-20 ng on column Fragrance Allergen [B] Experimental A Restek certified reference material (Catalog # 33103) was used in the experiment. Figure 11: Citronellol, Geraniol, Eugenol, and Methyl Eugenol linearity data results from measurement with VGA-100 Figure 12: Citronellol linearity plot showing VGA-100 measurement performance from 20 pg-20 ng on column

Fragrance Allergen [C] Experimental A Restek certified reference material (Catalog # 33104) was used in the experiment. Figure 13: Camphor, Coumarin, Iso-alpha-Methylionone, and Benzyl Cinnamate linearity data results from measurement with VGA-100 Figure 14: Coumarin linearity plot showing VGA-100 measurement performance from 20 pg-20 ng on column www.vuvanalytics.com 2017 VUV Analytics Inc. All rights reserved. Publication No. VUV100-IDL0001. VGA-100 and VUV Analytics are registered trademarks and are the property of VUV Analytics Inc. All other trademarks are the property of their respective owners. This information is provided for reference only. Although this information is believed to be accurate and reliable at the time of publication, VUV Analytics assumes no responsibility for errors or omissions.