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Then, 1 mL of gas from the gas vial was transferred to the test/reference vial.
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In this work, a highly reproducible standard gas generating vial is proposed.
The upper toluene phase containing the fatty acid methyl esters was collected and stored in a gas chromatograph vial at −20°C for analysis.
Samples were centrifuged and the upper hexane layer containing the FAME extract was transferred to a gas chromatography vial for analysis (Velasquez-Orta et al.2012).2012
Finally, the top phase (2/3) was removed and transferred into a gas chromatography vial and injected.
Microdissected tissues were transferred to a 2 ml glass gas chromatography vial using a pipette tip that had been dipped in water to reduce static.
Undiluted samples withdrawn for total dissolved inorganic carbon analysis, ∑CO2 aq), were immediately stored by filling gas tight vials to prevent equilibration with air at room temperature.
Blood and beverage samples were mixed with IS (n-propanol) at a ratio of 0.2/0.8 in the head space gas chromatography vials for ethanol testing.
The fatty acid methyl esters contained in the upper benzene phase were transferred to gas chromatography vials and stored at 4°C until injection into the chromatograph.
This was observed by mounting the electrochemical setup in a gas-tight vial.
Samples were evaporated to 1 mL and transferred to the gas chromatograph vials, which were previously spiked with recovery standards.
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