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Tg 5silms column

Manufactured by Thermo Fisher Scientific
Sourced in Italy

The TG-5SILMS column is a gas chromatography column designed for the separation and analysis of a wide range of organic compounds. It features a 5% phenyl-methylpolysiloxane stationary phase, which provides excellent selectivity and peak shape for a variety of analytes. The column has a length of 30 meters, an internal diameter of 0.25 millimeters, and a film thickness of 0.25 micrometers. The TG-5SILMS column is suitable for use in various applications, including environmental analysis, food testing, and pharmaceutical research.

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5 protocols using tg 5silms column

1

Gas Chromatography-Mass Spectrometry Protocol

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Gas-chromatographic separations were executed on a Trace 1310 (Thermo Scientific) equipped with TriPlus RSH auto sampler (Thermo Scientific) and coupled with a TSQ 8000 electron impact (EI) triple quadrupole mass spectrometer (Thermo Scientific). We used a TG-5SILMS column (Thermo Scientific) with the following dimensions: length 30 m; 0.25-mm inner diameter and 0.25-μm film. The column was operated with helium carrier gas using a PTV injector operating with a column flow 1.2 ml min−1 and a split less injection for 1 min. After initial 60 °C the temperature was raised to 320 °C at a rate of 14.5 °C min−1 and then held for 2 min. For cleaning, the temperature was increased to 350 °C and held for 5 min with a flow of 50 ml min−1. After split less time, the split flow was set to 20 ml min−1. The syringe was cleaned twice with 5 μl n-hexane each before injection and rinsed with 1 μl sample before the injection was done. After injection, the syringe was washed five times with ethyl acetate and five times with n-hexane (5 μl each). The GC oven program started at 100 °C for 1 min and the temperature was increased to 320 °C at 5 °C min−1, and held for 3 min. Measurement using the mass spectrometer was begun after 10 min of monitoring. The mass range between 50 and 650 m/z were monitored. The MS transfer line was set to 300 °C as well as the ion source temperature.
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2

GC-MS Analysis of Essential Oils

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Essential oils extracted after hydro-distillation, as well as all SPME samples, were run on a GC-MS system. GC-MS analysis was carried out using a Trace GC Ultra gas chromatograph coupled with a triple quadrupole mass spectrometer (TSQ Quantum XLS, Thermo Fisher Scientific, Milan, Italy). Injections were performed in split mode (1:50), and volatile compounds were chromatographed on a TG-5SILMS column (30 m × 0. 25 mm × 0. 25 μm) provided by Thermo Fisher Scientific (Milan, Italy), with helium as the carrier gas at a constant flow of 1.0 mL/min. The oven temperature was maintained at 40 °C for 3 min, and then increased to 200 °C at a rate of 5 °C/min, before being subsequently increased to 250 °C at a rate of 10 °C/min, and then finally held at 250 °C for 3 min. The inlet and ion source temperatures were both set at 230 °C, and MS was scanned at 70 eV in the electronic ionization mode. The mass spectra were acquired using the full-scan-monitoring mode, with a mass-scan range of m/z 29–448, equipped using the Xcalibur software (v. 2.2, Thermo Fisher Scientific).
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3

Pyrolysis-GC/MS Analysis of Lignin

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Py-GC/MS experiments
were conducted using a pyrolysis unit (GERSTEL PYRO with thermal desorption
unit GERSTEL TDU) which used a pulsed pyrolysis at temperatures ranging
from 350 to 1000 °C coupled with GC/MS Thermo Scientific Trace
1310 with a Thermo Scientific ISQ mass spectrometer using a TG-5SILMS
column (30 m × 250 μm × 0.25 μm). The pyrolysis
of the sample was performed in a quartz tube inside the heating chamber
under the helium atmosphere. The obtained pyrolysis gas was directly
transferred to the GC using a heated transfer line. No concentration
methods such as thermal desorption or cryo focusing were used. About
0.5 mg of lignin particles were loaded into the quartz pyrolysis tube
and the pyrolysis temperature was set to 450 or 600 °C. In the
pulse mode, the sample was placed on a cold pyrolysis probe, which
was rapidly (typically in the milliseconds range) heated to a predetermined
pyrolysis temperature and maintained for 0.33 min at that temperature.
The thermal desorption unit temperature was set to 280 °C like
the transfer temperature. GC column temperature program started at
45 °C for 5 min, followed by a gradient of 4 °C to the final
temperature of 280 °C and held for 15 min.
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4

Quantitative GC-MS Analysis of 2,3-DBPA

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Sample data were acquired using a Thermo ScientificTM ISQTM 7000 GC-MS system programed according to the method detailed by Surma et al., 2017 [28 (link)]. In brief, the carrier gas was helium and the injection port temperature was set to 260 °C. A 1.0 µL injection volume was volatilized for sample loading onto the TG5-SilMS column (Thermo Scientific cat. #26096-1420, 0.25 mm I.D., 0.25 µm film thickness, 30 m length), which was held at 60 °C for one min, then ramped 20 °C/min to 200 °C, held for 3 min at 200 °C, then ramped 30 °C/min to 250 °C, and held for 5 min at 250 °C. The GC-MS sample injector and detector interface temperatures were held at 260 °C. A calibration curve was generated for 2,3-DBPA (Alfa AesarTM, USA, 97%) over a concentration range of 1 µg/kg to 1000 mg/kg to assess the limit of detection and limit of quantitation of the instrument. An extracted ion analysis protocol was applied using the ChromeleonTM 7.2 software with a determined LOD of 1090 μg/kg and LOQ of 3310 μg/kg.
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5

Metabolic Profiling via GC-MS

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GC separation was conducted on a Thermo Trace 1300 GC fitted with a TraceGold TG-5SilMS column. 1 μl of derivatized sample was injected into the GC operating under the following conditions: split ratio = 20-1, split flow = 24 μl/min, purge flow = 5 ml/min, carrier mode = Constant Flow, and carrier flow rate = 1.2 ml/min. The GC oven temperature gradient was as follows: 80 °C for 3 min, increasing at a rate of 20 °C/min to 280 °C, and holding at a temperature at 280 °C for 8 min. For metabolic profiling, metabolites were detected using a Thermo ISQ 7000 mass spectrometer operated from 3.90 to 21.00 min in EI mode (−70eV) using select ion monitoring (SIM). For tracing, metabolites were detected in CI mode using SIM.
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