2020
DOI: 10.1071/en19134
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Data quality improvement for field-portable gas chromatography-mass spectrometry through the use of isotopic analogues for in-situ calibration

Abstract: Environmental contextQuantitative field-based sampling of airborne volatile organics continues to be a challenge because of the absence of laboratory supplies and facilities. Approaches are required to overcome poor data arising from difficulties with calibration of fielded instruments. This method normalises responses across portable thermal desorption gas-chromatography mass spectrometers and requires no advance calibration, enabling accurate and precise use of previously established response factors ported … Show more

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Cited by 12 publications
(3 citation statements)
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“…Qualley, A., Hughes, G.T., and Rubenstein, M.H. report on a method of improving the data in field-portable GS-MS by using the “pre-incorporation of isotopic analogues (of the target analytes) onto thermal desorption tubes in advance of field distribution …” [ 346 ].…”
Section: Instrumental Analysis Of Explosivesmentioning
confidence: 99%
“…Qualley, A., Hughes, G.T., and Rubenstein, M.H. report on a method of improving the data in field-portable GS-MS by using the “pre-incorporation of isotopic analogues (of the target analytes) onto thermal desorption tubes in advance of field distribution …” [ 346 ].…”
Section: Instrumental Analysis Of Explosivesmentioning
confidence: 99%
“…Za prijenosne GC-MS uređaje obično se upotrebljavaju kraće kolone (duljine 5 -15 m, unutarnjeg promjera 0,10 -0,25 mm i debljine premaza 0,4 -0,1 µm). 21,22 Primjenjuju se različite tehnike ionizacije (kemijska ionizacija, ionizacija elektronima, elektroraspršenje), a kao metoda uvođenja uzorka najčešće se primjenjuje injektiranje tekućine s mikroekstrakcijom na čvrstoj fazi i toplinskom desorpcijom. 19,[23][24][25][26] Prijenosni GC-MS uređaji većinom rade na principu hvatanja iona (engl.…”
Section: Prijenosna Gc-ms Detekcijaunclassified
“…EME combined with HPLC-UV detection technique has been applied for the determination of melamine in the range of 7-8000 ng mL -1 (LOD of 2.0 -5.8 ng mL −1 ), with enrichment factor in the range of . In this approach, the extraction time was 15 min, which is much shorter when compared with the HF-LPME technique (60 min) that provided a detection limit of 0.003 mg kg -1 [72,73]. For exposed solvent microextraction modes, SDME and DLLME are among the popular techniques preferred by analytical chemists.…”
Section: Liquid-phase Microextraction Techniquesmentioning
confidence: 99%