Measurement of Hydroxy Carbonyls and Other Carbonyls in Ambient Air Using Pentafluorobenzyl Alcohol as a Chemical Ionization Reagent

1999 ◽  
Vol 71 (16) ◽  
pp. 3420-3427 ◽  
Author(s):  
Reggie S. Spaulding ◽  
Paul Frazey ◽  
Xin Rao ◽  
M. Judith Charles
1989 ◽  
Vol 24 (6) ◽  
pp. 435-438 ◽  
Author(s):  
R. Srinivas ◽  
M. Vairamani ◽  
G. K. Viswanadha Rao ◽  
U. A. Mirza

2020 ◽  
Author(s):  
Yi Ji ◽  
L. Gregory Huey ◽  
David J. Tanner ◽  
Young Ro Lee ◽  
Patrick R. Veres ◽  
...  

Abstract. A new ion source (IS) utilizing vacuum ultraviolet (VUV) light is developed and characterized for use with iodide-chemical ionization mass spectrometers (I−-CIMS). The VUV-IS utilizes a compact krypton lamp that emits light in two wavelength bands corresponding to energies of ~10.0 and 10.6 eV. The VUV light photoionizes either methyl iodide (ionization potential, IP = 9.54 ± 0.02 eV) or benzene (IP = 9.24378 ± 0.00007 eV) to form cations and photoelectrons. The electrons react with methyl iodide to form I− which serves as the reagent ion for the CIMS. The VUV-IS is characterized by measuring the sensitivity of a quadrupole CIMS (Q-CIMS) to formic acid, molecular chlorine, and nitryl chloride under a variety of flow and pressure conditions. The sensitivity of the Q-CIMS, with the VUV-IS, reached up to ~700 Hz pptv−1, with detection limits of less than 1 pptv for a one minute integration period. The reliability of the Q-CIMS with a VUV-IS is demonstrated with data from a month long ground-based field campaign. The VUV-IS is further tested by operation on a high resolution time-of-flight CIMS (TOF-CIMS). Sensitivities greater than 25 Hz pptv−1 were obtained for formic acid and molecular chlorine, which were similar to that obtained with a radioactive source. In addition, the mass spectra from sampling ambient air was cleaner with the VUV-IS on the TOF-CIMS compared to measurements using a radioactive source. These results demonstrate that the VUV lamp is a viable substitute for radioactive ion sources on I−-CIMS systems for most applications. In addition, the VUV-IS can likely be extended to other reagent ions, such as SF6− which are formed from high IP electron attachers, by the use of absorbers such as benzene to serve as a source of photoelectrons.


1990 ◽  
Vol 25 (10) ◽  
pp. 497-502 ◽  
Author(s):  
Charles Allgood ◽  
Yi Lin ◽  
Yee-Chung Ma ◽  
Burnaby Munson

1982 ◽  
Vol 54 (7) ◽  
pp. 1245-1247 ◽  
Author(s):  
W. D. Reents ◽  
R. C. Burnier ◽  
Robert B. Cody ◽  
Ben S. Freiser

2012 ◽  
Vol 26 (8) ◽  
pp. 940-942 ◽  
Author(s):  
Putuma P. Gqamana ◽  
Penggao Duan ◽  
Mingkun Fu ◽  
Vanessa Gallardo ◽  
Hilkka I. Kenttämaa

2009 ◽  
Vol 7 (3) ◽  
pp. 312-316 ◽  
Author(s):  
Fadel Alwedian ◽  
Khalid Abu-Shandi

AbstractThe selective enhancement of membrane introduction mass spectrometry for non-polar alkanes, alkenes, and aromatic hydrocarbon compounds by the application of acetonitrile as a chemical ionization reagent was investigated. Acetonitrile Cl is able to produce specific fragment ions for many of the compounds test and this can be used to identify and quantify the parent neutrals. This method provided relatively high detection limits of the test compounds. This method could potentially be useful for analytical applications such as the detection of non-polar hydrocarbons for environmental studies if CH3CN Cl/MIMS is coupled with a preconcentration method.


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