Evaluation of a Commercial Mass Spectrometer for Its Potential To Measure Auto Exhaust Constituents in Real Time

1999 ◽  
Vol 38 (6) ◽  
pp. 2203-2209 ◽  
Author(s):  
Mark A. Dearth
Energies ◽  
2021 ◽  
Vol 14 (8) ◽  
pp. 2123
Author(s):  
Makuachukwu F. Mbaegbu ◽  
Puspa L. Adhikari ◽  
Ipsita Gupta ◽  
Mathew Rowe

Determining gas compositions from live well fluids on a drilling rig is critical for real time formation evaluation. Development and utilization of a reliable mass spectrometric method to accurately characterize these live well fluids are always challenging due to lack of a robust and effectively selective instrument and procedure. The methods currently utilized need better calibration for the characterization of light hydrocarbons (C1–C6) at lower concentrations. The primary goal of this research is to develop and optimize a powerful and reliable analytical method to characterize live well fluid using a quadruple mass spectrometer (MS). The mass spectrometers currently being used in the field have issues with detection, spectra deconvolution, and quantification of analytes at lower concentrations (10–500 ppm), particularly for the lighter (<30 m/z) hydrocarbons. The objectives of the present study are thus to identify the detection issues, develop and optimize a better method, calibrate and QA/QC the MS, and validate the MS method in lab settings. In this study, we used two mass spectrometers to develop a selective and precise method to quantitatively analyze low level lighter analytes (C1–C6 hydrocarbons) with masses <75 m/z at concentrations 10–500 ppm. Our results suggest that proper mass selection like using base peaks with m/z 15, 26, 41, 43, 73, and 87, respectively, for methane, ethane, propane, butane, pentane, and hexane can help detect and accurately quantify hydrocarbons from gas streams. This optimized method in quadrupole mass spectrometer (QMS) will be invaluable for early characterization of the fluid components from a live hydrocarbon well in the field in real time.


2021 ◽  
Author(s):  
Antonia Zogka ◽  
Manolis N. Romanias ◽  
Frederic Thevenet

Abstract. Formaldehyde (FM) and glyoxal (GL) are important atmospheric species of indoor and outdoor environments. They are either directly emitted in the atmosphere or they are formed through the oxidation of organic compounds by indoor and/or outdoor atmospheric oxidants. Despite their importance, the real-time monitoring of these compounds with soft ionization mass spectrometric techniques, e.g. proton transfer mass spectrometry (PTR-MS), remains problematic and is accompanied by low sensitivity. In this study, we evaluate the performance of a multi-ion selected ion flow tube mass spectrometer (SIFT-MS) to monitor in real-time atmospherically relevant concentrations of FM and GL under controlled experimental conditions. The SIFT-MS used is operated under standard conditions (SC), as proposed by the supplier, and customized conditions (CC), to achieve higher sensitivity. In the case of FM, SIFT-MS sensitivity is marginally impacted by RH, and the detection limits achieved are below 200 ppt. Contrariwise, in the case of GL, a sharp decrease of instrument sensitivity is observed with increasing RH when the H3O+ ion is used. Nevertheless, the detection of GL using NO+ precursor ion is moderately impacted by moisture with an actual positive sensitivity response. Therefore, we recommend the use of NO+ precursor for reliable detection and quantitation of GL. This work evidences that SIFT-MS can be considered as an efficient tool to monitor the concentration of FM and GL using SIFT-MS in laboratory experiments and potentially in indoor or outdoor environments. Furthermore, SIFT-MS technology still allows great possibilities for sensitivity improvement and high potential for monitoring low proton transfer affinity compounds.


BMC Chemistry ◽  
2019 ◽  
Vol 13 (1) ◽  
Author(s):  
Jenni Hawke ◽  
Graham Errington ◽  
Matthias Bente von Frowein

AbstractMainstream tobacco smoke is a complex and dynamic aerosol, consisting of particulate and vapour phases. Most approaches to determine mainstream smoke toxicant yields are based on offline techniques that limit the opportunity to observe in real time the processes leading to smoke formation. The recent development of online real-time analytical methods offers many advantages over traditional techniques. Here we report the LM2X-TOFMS (Borgwaldt GmbH, Germany), a commercial instrument that couples a linear smoking engine with a time-of-flight mass spectrometer for real-time per-puff measurement of the vapour phase of mainstream cigarette smoke. Total cigarette and puff-by-puff (μg/puff) yields were evaluated, in line with International Council of Harmonisation recommendations, for seven smoke toxicants: acetaldehyde, acetone, 1,3-butadiene, 2-butanone, benzene, isoprene and toluene. Measurements were unaffected by small system changes including replacing the sampling capillary or time of day (all P > 0.05), indicating that the LM2X-TOFMS is rugged. Control charts showed that the system has good stability and control. Analysis of certified gas mixtures of six concentrations of each analyte showed a highly linear response for all seven analytes (R2 = 0.9922–0.9999). In terms of repeatability, the lowest variation was observed for isoprene with a coefficient of variation (CV) of < 6% for each concentration. Acetaldehyde showed the highest CV, increasing from 8.0 to 26.6% with decreasing gas concentration. Accuracy was analysed in terms of relative error, which was ± 16% for six of the analytes; however, the relative error for acetaldehyde was (− 36.2%), probably due to its low ionisation efficiency under the instrument’s vacuum ultraviolet lamp. Three cigarette products (reference and commercial) with different ISO tar levels were analysed by the LM2X-TOFMS puff by puff under ISO regulatory smoking conditions. The relative standard deviation based on average yield per cigarette for each analyte in each product (summed puffs per product, n = 30) ranged from ≤ 9.3 to ≤ 16.2%. Measurements were consistent with published data per cigarette. In conclusion, the LM2X-TOFMS is suitable for determining the vapour-phase yields of seven analytes on a real-time, puff-by-puff basis, and can be utilised for both fast screening (qualitative) and quantitative measurements of mainstream cigarette smoke.


2014 ◽  
Vol 26 (2) ◽  
pp. 212-223 ◽  
Author(s):  
Ryan J. Bell ◽  
Nicholas G. Davey ◽  
Morten Martinsen ◽  
Christian Collin-Hansen ◽  
Erik T. Krogh ◽  
...  

2002 ◽  
Vol 21 (8) ◽  
pp. 515-525 ◽  
Author(s):  
Jorge Andres Diaz ◽  
Andres E.Mora Vargas ◽  
Franklin Chang Diaz ◽  
Jared P Squire ◽  
Verlin Jacobson ◽  
...  

2014 ◽  
Vol 568-570 ◽  
pp. 395-400
Author(s):  
Kai Ni ◽  
Xiang Yan ◽  
Quan Yu ◽  
Zu Hua Shi ◽  
Xin Qiong Lu ◽  
...  

Air core transformer is an essential part of mass spectrometer. Test coil is often used to measure its resonant frequency with the advantages of easy installation and high sensitivity. However, the influence of test coil while it is installed close to the working coils on the transformer is not studied before. To reveal the influence of test coil and determine the right position to install, two experiments using test coil and opened probe respectively for the measurement are conducted. Since the opened probe has little load effect on the original transformer impedance system, it can be used to validate the influence of test coil. By comparing the two experimental results, we find that the right position to install the test coil is on the further side of the primary coil to the secondary coil. This work allows us to integrate the test coil with the air core transformer to monitor the resonant frequency in real-time.


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