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Rt q bond

Manufactured by Restek
Sourced in United States, Canada

RT-Q-Bond is a fused silica-based capillary column designed for gas chromatography applications. It features a bonded stationary phase that provides high thermal stability and inertness, allowing for the separation of a wide range of analytes.

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3 protocols using rt q bond

1

Photocatalytic Degradation of Pollutants

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Photocatalytic runs were carried out in a 250 mL Pyrex photoreactor equipped with a mechanic agitator (500 rpm) and a gas inlet and outlet for gas sampling and purge. A 18W PL-L lamp (Philips, Amsterdam, The Netherlands), placed below the photoreactor, was chosen as the UVA source with a UV band of 350-410 nm centred at 370 nm (irradiance of 5 mW.cm−2).
We introduced 100 mL of a 1.0 vol% PA solution containing 50 mg of photocatalyst into the reactor. A continuous flow of argon (70 mL.min−1) was applied through a bubbler for 6 h into the system to fully remove the ambient air. After the purge, the photoreactor was sealed and irradiated with UVA light. Every 65 min, a 2 mL aliquot of photoproduced gases in the headspace was carried by vacuum pumping into a Clarus 500 GC FID-PDHID (PerkinElmer, Waltham, MA, USA) for analysis. Products were firstly separated though a RT-Q-Bond (Restek–30 m × 0.53 mm × 20 μm) column before FID with a Polyarc methanization module. For PDHID, a RT-M5A molecular sieve (Restek–30 m × 0.32 mm × 30 μm) was added. The carrier gas was helium N60 grade (Messer, Bad Soden, Germany). For each gaseous analysis, the oven temperature was set at 50 °C rising at 20 °C/min to reach a maximum temperature of 150 °C maintained for an additional 55 min. Tests were repeated twice to ensure reproducibility.
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2

Investigating Multiplex Injector Configurations

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The instrumentation used for the investigation of different multiplex injector configurations was a GC-2010 Plus gas chromatograph with a Tracera BID barrier-discharge ionization detector equipped with an external 6-port switching valve from Shimadzu (Kyoto, Japan). The column was a DB-5MS (5% phenyl-95% methyl-polysiloxane) 30 m × 0.25 mm × 0.25 μm from Agilent J&W. A GC-MS-QP2010 Plus instrument (Shimadzu) equipped with a Rt-Q-BOND (100% divinylbenzene, Restek, Bellefonte, PA, USA) PLOT (porous layer-open tubular) column of 30 m × 0.32 mm × 10 μm dimension equipped with a particle trap and a guard column was used for real sample analysis. For the laboratory-made injector, an Arduino Leonardo ETH board (RS Components, Frankfurt am Main, Germany) with a code written in-house for Arduino Software (IDE) v1.8.9 (https://www.arduino.cc/en/main/software, accessed on 30 December 2023) was used for the control of the solenoid valves. The normally open 2-way, normally closed 2-way and 3-way solenoid valves used for the work were purchased from Bürkert Austria GmbH (Vienna, Austria). Tee connectors were from VICI Valco (Schenkon, Switzerland).
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3

Quantification of N2O by GC-MS

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N 2 O concentration was analyzed using a gas chromatograph (GC Clarus 680) coupled to a mass spectrometer (Clarus SQ 8T; Perkin Elmer, USA). The GC was calibrated at the beginning of each day with certified calibration gas mixture of N 2 O at 2 ppmv (BOC GAZ, Canada) and each of the four unknown samples. The samplers were placed in the thermostated oven compartment for 2 min at 50 °C. Afterwards, the samples were pressurized for 2 min at 110.32 kPa. A gas sample volume of 100 μl was injected into an analytical column Rt-Q-bond (30 m × 0.25 mm i.d., 8-μm film, Restek, Canada) using 0.9 ml/min of He as carrier gas. The temperature in the GC injector was kept at 100 °C and the temperature in the oven was 30 °C for 4 min, then it was increased to 150 °C at 100 °C/min and kept constant for 1 min. For these conditions, the N 2 O peak was observed at 3.42 min. The interface temperature between column and MS detector was 150 °C. An electron impact ionization of 70 eV and an ion source temperature of 220 °C were used. The mass spectrometer was used in SIM mode.
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