scholarly journals Rapid, low-cost, and in-situ analysis of per- and polyfluoroalkyl substances in soils and sediments by ambient 3D-printed cone spray ionization mass spectrometry

Chemosphere ◽  
2021 ◽  
Vol 272 ◽  
pp. 129708
Author(s):  
Hilary M. Brown ◽  
Patrick W. Fedick
2001 ◽  
Vol 81 (3) ◽  
pp. 249-254 ◽  
Author(s):  
Morris Schnitzer

Traditionally, studies on soil organic matter (SOM) begin with the extraction of SOM from soils, its fractionation into humic acid, fulvic acid, and humin, followed by de-ashing of each fraction. These are tedious, laborious and inefficient procedures that do not provide any chemical information on these materials. Instead, recently developed methods such as solid-state 13C NMR and pyrolysis – field ionization mass spectrometry (Py-FIMS) can now be used for the in situ analysis of SOM in soils. These methods identify the major chemical components of SOM without extractions and fractionations, and yield valuable information on the main chemical structures in these materials. A better knowledge of the structural chemistry of SOM will help SOM chemists and other soil scientists to better understand the complex chemical and biochemical reactions that occur in soils, and will enable them to develop practices that will improve soil management and soil productivity. Key words: Extraction, fractionation, solid state 13C NMR, pyrolysis-field ionization mass spectrometry, chemical composition


RSC Advances ◽  
2015 ◽  
Vol 5 (92) ◽  
pp. 75395-75402 ◽  
Author(s):  
Xiaoqin Zhong ◽  
Liang Qiao ◽  
Baohong Liu ◽  
Hubert H. Girault

Direct coupling of ESTASI-MS with both hydrophilic and hydrophobic TLC for ambient in situ analysis and imaging with ultralow sample consumption.


2009 ◽  
Vol 2 (1) ◽  
pp. 119-151 ◽  
Author(s):  
J. P. Kercher ◽  
T. P. Riedel ◽  
J. A. Thornton

Abstract. We report a new method for the simultaneous in situ detection of nitryl chloride (ClNO2) and dinitrogen pentoxide (N2O5) using chemical ionization mass spectrometry (CIMS). The technique relies on the formation and detection of iodide ion-molecule clusters, I(ClNO2)− and I(N2O5)−. The novel N2O5 detection scheme is direct. It does not suffer from high and variable chemical interferences, which are associated with the typical method of nitrate anion detection. We address the role of water vapor, electric field strength, and instrument zero determinations, which influence the overall sensitivity and detection limit of this method. For both species, the method demonstrates high sensitivity (>1 Hz/pptv), precision (~10% for 100 pptv in 1 s), and accuracy (~20%), the latter ultimately determined by the nitrogen dioxide (NO2) cylinder calibration standard and characterization of inlet effects. For the typically low background signals (<10 Hz) and high selectivity, we estimate signal-to-noise (S/N) ratios of 2 for 1 pptv in 60 s averages, but uncertainty associated with the instrumental zero currently leads to an ultimate detection limit of ~5 pptv for both species. We validate our approach for the simultaneous in situ measurement of ClNO2 and N2O5 while on board the Research Vessel (RV) Knorr as part of the ICEALOT 2008 Field Campaign.


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