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Tenax ta sorbent

Manufactured by Merck Group
Sourced in Germany

Tenax TA is a porous polymer-based sorbent material used for the collection and analysis of volatile organic compounds (VOCs) in air and gas samples. It is a highly inert and thermally stable material, designed to provide efficient adsorption and desorption of a wide range of organic compounds. The core function of Tenax TA is to serve as a sample collection medium for analytical techniques, such as thermal desorption and gas chromatography, to enable the identification and quantification of VOCs in various environmental and industrial applications.

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2 protocols using tenax ta sorbent

1

Microfabricated Sorbent Chip for VOC Sampling

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We used a previously published microfabricated sorbent chip18 (link) in our newly described wearable system. Briefly, a chip is created using traditional photolithography and etching into a glass substrate. Resistive heaters are patterned onto the back side of the device allowing for rapid heating and desorption of VOCs. Tenax TA sorbent (Sigma-Aldrich, St. Louis, MO) is packed into the chip, which allows for broad spectrum sampling and quantification of many VOCs of interest. The chip can be tailored with other sorbents if specific chemical sampling is desired, which was outside the scope of this current work.
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2

Thermal decomposition of lignin

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The Shimadzu TD-20 thermal desorption system was used for the low-temperature, slow-heat-rate thermal decomposition of lignin. The GC/MS analysis of the lignin decomposition products was performed using a Shimadzu QP-2010 Plus gas chromatograph–mass spectrometer (Kyoto, Japan). The thermal desorption parameters were as follows: helium was used as the carrier gas flowing at 30 mLmin−1, and the volatile and semi-volatile products of lignin decomposition were trapped on the Tenax TA sorbent (Sigma Aldrich, Steinheim, Germany) in a cooling trap at −10 °C. The lignin sample weight was varied from 0.6 mg to 8.1 mg. Thermal decomposition was carried out in the range of 150–400 °C in 50 °C increments. The duration of the process was varied from 5 to 60 min.
The GC separation parameters were constant during all experiments. The GC was equipped with a HP-5MS fused-silica capillary column (30 m × 0.25 mm i.d., 0.25 µm f.t.). The gas flow was 1.0 mLmin−1 with the split ratio of 30:1. The GC oven temperature program began at 40 °C and then increased at a heating rate of 3 °C/min to 200 °C followed by a post-run program at 320 °C for 3 min. The MS was operated in EI mode (70 eV) at 230 °C. The components were identified using the NIST and Wiley libraries.
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