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Rxi 624sil

Manufactured by Restek
Sourced in United States

The Rxi-624Sil is a capillary gas chromatography column designed for the separation and analysis of a wide range of volatile organic compounds. It features a 624-type stationary phase that provides excellent peak shape and resolution for a variety of analytes, including alcohols, ketones, and halogenated compounds. The column is inert, thermally stable, and suitable for use with a variety of sample types and detection methods.

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5 protocols using rxi 624sil

1

Comprehensive Volatile Analysis by GC×GC-TOF MS

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The analyses of volatile molecules were carried out using a Pegasus 4D (LECO Corp., St. Joseph, MI, United States) GC×GC time-of-flight (TOF) MS instrument with an Agilent 6890 GC, and equipped with an MPS autosampler (Gerstel, Linthicum Heights, MD, United States). The first dimension column was an Rxi-624Sil (60 m × 250 μm × 1.4 μm (length × internal diameter × film thickness)) connected in series with a Stabilwax secondary column (1 m × 250 μm × 1.4 μm), both from Restek (Bellefonte, PA, USA). The carrier gas was helium, at a flow rate of 2 mL/min. The primary oven temperature program was 35°C (hold 1 min) ramped to 230°C at a rate of 3.5°C/min. The secondary oven and the thermal modulator were offset from the primary oven by +5°C and +25°C, respectively. A modulation period of 2.0 s (alternating 0.5 s hot and 0.5 s cold pulses) was used. The transfer line temperature was set at 250°C. A mass range of m/z 30 to 500 was collected at a rate of 200 spectra/s following a 2.5 min acquisition delay. The ion source was maintained at 200°C. Data acquisition and analysis were performed using ChromaTOF software, version 4.50 (LECO Corp).
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2

GC×GC-TOF MS Volatilome Analysis

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The TD tubes were desorbed into a Pegasus 4D (LECO Corporation, St. Joseph, MI) GC × GC-TOF MS instrument with an Agilent 7890 GC equipped with a TD unit, cooled injection system (CIS), and a Multi-Purpose Sampler (MPS) autosampler (Gerstel, Linthicum Heights, MD). The solvent venting time was 10 min (30 °C; 60 ml min−1), cryofocusing time was 5 min (−100 °C), sample desorption time was 180 s, CIS temperature was 330 °C, and the injection mode was splitless. Chromatographic analysis was performed using an Rxi-624Sil (60 m × 250 μm × 1.4 μm) as the first dimension (1D)-GC column and a Stabilwax (1.5 m × 250 μm × 0.5 μm) as second dimension (2D)-GC column, both purchased from Restek (Bellefonte, PA, US). The modulation time was 2 s total and helium as the carrier gas (flowrate: 2 ml min−1). TOF MS was employed as a detector, with the following parameters: electron impact at 70 eV; acquisition range: 30–500 mz−1; acquisition rate: 200 spectra/s; and ion source temperature: 200 °C. Data acquisition and analysis was performed using ChromaTOF software, version 4.50 (LECO Corporation).
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3

Comprehensive GC×GC-TOF-MS Analysis of Complex Samples

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A Pegasus 4D (LECO Corporation, St. Joseph, MI) GC ×GC time-of-flight (TOF) MS instrument with an Agilent 6890N GC, and an MPS autosampler (Gerstel, Linthicum Heights, MD, USA) equipped with a cooled sampler tray (4 °C), was used. The primary column was an Rxi-624Sil (60 m ×250 μm ×1.4 μm) connected in series with a Stabilwax secondary column (1 m ×250 μm ×1.4 μm) from Restek (Bellefonte, PA, USA). The carrier gas was helium, at a flow rate of 2 ml min−1. The primary oven temperature program was 35 °C (hold 1 min) ramped to 230 °C at a rate of 5 °C min−1. The secondary oven and the thermal modulator were offset from the primary oven by +5 °C and +25 °C, respectively. A modulation period of 2.5 s (alternating 0.75 s hot and 0.5 s cold) was used. The transfer line temperature was set at 250 °C. A mass range of m/z 30 to 500 was collected at a rate of 200 spectra/s following a 3 min acquisition delay. The ion source was maintained at 200 °C. Data acquisition and analysis was performed using ChromaTOF software, version 4.50 (LECO Corp.).
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4

GC-GCxToF-MS Analysis of Breath Volatiles

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One liter Tedlar bags (SKC Inc, Eighy Four, PA, US) were used for the collection of breath [22] .
A three-bed TD tube containing Carbopack Y, X, and Carboxen 1000 (Supelco, Bellefonte, PA), a sorbent combination previously optimized for the collection of a wide range of breath molecules, was used to concentrate and store volatile molecules [15] . TD tubes were desorbed in a Pegasus 4D (LECO Corporation, St. Joseph, MI) GC×GC-ToFMS instrument with an Agilent 7890 GC equipped with a TDU, CIS, and MPS autosampler (Gerstel, Linthicum Heights, MD). Solvent venting time: 10 min (30°C; 60 mL/min); cryofocusing time: 5 min (-100°C), sample desorption time: 180s; CIS temperature: 330°C; injection mode: splitless. Chromatographic analysis was performed using a Rxi-624Sil (60m×250μm×1.4μm) as 1 D-GC column and a Stabilwax (1.5m×250μm×0.5μm) as 2 D-GC column, both purchased from Restek (Bellafonte, PA, US).
Modulation time was 2 sec total and helium as carrier gas (flow-rate: 2 mL/min). For detecting breath molecules, a ToFMS was employed, with the following parameters: electron impact at 70 eV; acquisition range: 30-500 m/z; acquisition rate: 200 spectra/s; ion source temperature: 200°C.
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5

GC×GC-TOF-MS Analysis of Complex Samples

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A Pegasus 4D (LECO Corporation, St. Joseph, MI) GC×GC time-of-flight (TOF) MS instrument with an Agilent 7890 GC, and an MPS autosampler (Gerstel, Linthicum Heights, MD, USA) equipped with a cooled sampler tray (4 °C), was used. The primary column was an Rxi-624Sil (60 m × 250 µm × 1.4 µm) connected in series with a Stabilwax secondary column (1 m × 250 µm × 1.4 µm) from Restek (Bellefonte, PA, USA). The carrier gas was helium, at a flow rate of 2 mL/min. The primary oven temperature program was 35 °C (hold 1 min) ramped to 230 °C at a rate of 5 °C/min. The secondary oven and the thermal modulator were offset from the primary oven by +5 °C and +25 °C, respectively. A modulation period of 2.5 s (alternating 0.75 s hot and 0.5 s cold) was used. The transfer line temperature was set at 250 °C. A mass range of m/z 30 to 500 was collected at a rate of 200 spectra/s following a 3 min acquisition delay. The ion source was maintained at 200 °C. Data acquisition and analysis was performed using ChromaTOF software, version 4.50 (LECO Corp.).
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