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Documentation in support of your JEOL product.

Introduction of latest GC/HR-TOFMS system: JMS-T200GC AccuTOF-GCx - High Mass Accuracy and Stability

JEOL has recently announced a 4th generation GC/HR-TOFMS system, the JMS-T200GC AccuTOF-GCx, in 2015. The AccuTOF-GCx offers high sensitivity, high mass resolving power, high mass accuracy, and a wide dynamic range in combination with high-speed data acquisition. In this application note, we show we show high mass accuracy and m/z stability using this latest GC/HR-TOFMS system.

Identification and distribution analysis of additives in a molded NBR by PY/GCxGC/HRTOFMS

The characteristics of polymeric materials vary depending on the additives. Consequently, a variety of additives can be added into the raw polymer resin in order to achieve the required characteristics for the product. PY/GC/MS is often used as an analytical method for the analysis of polymeric materials. However, PY/GC/MS is often insufficient for the chromatographic separation of additives and thermal decomposition products from the polymer. As a result, it is often difficult to assign compound identities. On the other hand, comprehensive two-dimensional gas chromatography/high resolution time-of-flight mass spectrometry (GCxGC/HRTOFMS) is a well-known technique that provides high chromatographic separation by using two different polarity GC columns. Additionally, when this technique is used with high resolution mass measurements, it can be a powerful tool for estimating elemental compositions of analytes found within a complex mixture. In this application note, the additives were identified within a commercially available molded polymer by using pyrolysis (PY)/GCxGC/HRTOFMS.

High-speed 50 Hz Data AcquisitionCapability for Comprehensive 2-dimensional GC Measurements

The comprehensive 2-dimensional GC (GC x GC) technique provides higher-separation capabilities for complex mixtures than the typical 1-dimensional GC measurements. However, the GC x GC technique requires high speed data acquisition, e. g. > 20 Hz, for the GC detectors due to the shorter 2nd GC column which elutes samples within just a few seconds (comparable to those used for the ultra-fast GC measurements). Recently, JEOL has developed a new generation GC-HRTOFMS system called the “AccuTOF GCv 4G”. The AccuTOF GCv 4G has high sensitivity, high resolution, high mass accuracy and high speed data acquisition, all simultaneously. In fact, this instrument can measure data using up to a 50 Hz data acquisition speed which is more than sufficient to do not only fast GC measurements but also GC x GC measurements.

Group-type Analysis of Crude Oil by Using GC/FI-TOFMS Part 2: Reproducibility of group-type analysis results

Field Desorption (FD) and Field Ionization (FI) are both techniques that ionize analytes by electron tunneling from the analyte molecules to a solid surface (emitter) in a high electric field. In the case of FD, the sample is applied directly onto the emitter and heated by applying an electric current through the emitter for desorption and ionization. In the case of FI, vaporized analyte molecules are introduced into the proximity of the emitter. Both FI and FD are soft ionization methods that generally yield intact molecular ions and, in most cases, produce very few fragment ions. Generally, these two techniques are used to ionize analytes that are easy to fragment and do not generally produce molecular ions during electron ionization (EI), such as hydrocarbons in crude oil.

Group-type Analysis of Crude Oil by Using GC/FI-TOFMS Part 1: Determination of average molecular weights

Field Desorption (FD) and Field Ionization (FI) are both techniques that ionize analytes by electron tunneling from the analyte molecules to a solid surface (emitter) in a high electric field. In the case of FD, the sample is applied directly onto the emitter and heated by applying an electric current through the emitter for desorption and ionization. In the case of FI, vaporized analyte molecules are introduced into the proximity of the emitter. Both FI and FD are soft ionization methods that generally yield intact molecular ions and, in most cases, produce very few fragment ions. Generally, these two techniques are used to ionize analytes that are easy to fragment and do not generally produce molecular ions during electron ionization (EI), such as hydrocarbons in crude oil.

GCxGC-EI and GCxGC-FI Measurements Using the EI-FI Combination Ion Source

Comprehensive 2-dimensional GC (GC x GC) provides higher-separation capabilities for complex mixtures than the typical 1-dimensional GC measurements. However, this technique requires high speed data acquisition, e. g. > 20 Hz, for the GC detectors due to the shorter 2nd GC column (comparable to those used for the ultra-fast GC measurements) which elutes samples within just a few seconds. Recently, JEOL has developed a new generation GC-HRTOFMS system called the “AccuTOF GCv 4G”. The AccuTOF GCv 4G has high sensitivity, high resolution, high mass accuracy and high speed data acquisition, all simultaneously. Also JEOL has developed a unique EI/FI combination ion source for this system which provides the capabilities of GC/EI and GC/FI measurements without having to break vacuum in order to switch between each ionization mode. Additionally, this combination is particularly powerful in that it provides library searchable fragmentation information by using EI and high mass accuracy molecular ion information by using FI.

GCxGC TOFMS Analysis of Base Oils with CI, PI, FI

Structural elucidation of hydrocarbon classes in petroleum products are always in high demand. Comprehensive two-dimensional gas chromatography time-of-flight mass spectrometry (GCxGC-TOFMS) with electron ionization (EI) is a powerful method for characterizing complex mixtures such as base oils. However, EI data can often lack a strong molecular ion signal. Therefore, it is necessary to measure samples with soft-ionization methods such as positive chemical ionization (PCI), field ionization (FI), or photo-ionization (PI) for the detection of molecular ions. Each technique is a little different so it is important to understand the characteristics of each soft ionization method. In this application note, we compare the mass spectra of a base oil analyzed by GCxGC-TOFMS with EI, PCI, FI, and PI.

Analysis of High Boiling Point Compounds - Cholesterol and Irganox® 1010

The high boiling point compounds cholesterol and Irganox® 1010, an anti-oxidant additive for polymers, were analyzed by GC/MS. The analyses were performed using electron ionization (EI) and field ionization (FI), which is a soft ionization method, to show the difference in mass spectral patterns that result from these two ionization techniques.

Features and Applications of Newly-Developed GC-TOFMS “The AccuTOF GC”

A gas-chromatograph mass spectrometer (GC-MS) is a combined analyzer that has superior ability in analyzing organic compounds qualitatively and quantitatively. The first part, gas chromatograph, separates the compounds included in a sample (mixture), then the second part, mass spectrometer, obtains mass spectra of the compounds to carry out qualitative analysis. Quantitative analysis can be carried out as well from the peak area of the mass chromatogram of the compound. As a mass spectrometer of a GC-MS system, several types of mass spectrometers are on the market, such as magnetic field, quadrupole (QMS), ion trap (ITD), and time-of-flight (TOF). Each mass spectrometer has its own features and applications.

Examining Selectivity by Using High Resolution Mass Chromatography

Transformer oil containing no PCBs was diluted 10,000 times, and then this solution was spiked with a mixture of commercially available PCBs (KC-500). The resulting sample was analyzed by using the JEOL AccuTOF-GC with FastGC/MS conditions. Afterwards, the data was examined by varying the mass range window (called "window width") used for the PCB reconstructed ion chromatogram (RIC) to determine if the effect of the background impurities can be eliminated so that the analyte peaks are easily observed in the resulting data.

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