Literature DB >> 31392701

An Automated Method for Chemical Composition Analysis of Lubricant Base Oils by Using Atmospheric Pressure Chemical Ionization Mass Spectrometry.

Jeremy Manheim1, Yuyang Zhang1, Jyrki Viidanoja2,3, Hilkka I Kenttämaa4.   

Abstract

Since its invention in the 1950s, field ionization mass spectrometry (FI MS) has been, and currently is, the go-to technique employed by the petrochemical industry for the identification of the different types of nonvolatile compounds in their products. Unfortunately, FI MS has several inherent drawbacks, such as poor reproducibility. The performance of positive-ion mode atmospheric pressure chemical ionization mass spectrometry (APCI MS) with O2 gas as the sheath/auxiliary gas and a saturated hydrocarbon solvent/reagent was recently compared with that of FI MS and found to show promise as an alternative, highly reproducible method for lubricant base oil analysis. We report here on the automation of the APCI/O2/saturated hydrocarbon MS method. Isooctane was chosen as the optimal APCI solvent/reagent for base oil ionization due to the low level of fragmentation it provided for model compound mixtures. Three minutes was determined to be the shortest possible cleaning time between samples, regardless of the base oil viscosity. The total analysis time for each sample was 5 min. The reproducibility of the method was assessed by determining within-day and between-day precisions and total precision for hydrocarbon class distributions measured for three different base oils. All total precision values were found to be better than 6.2%, suggesting that the automated (+)APCI/O2/isooctane method is reproducible and robust.

Entities:  

Keywords:  APCI; Automated; Base oils; Carbenium ions; Hydrocarbons; Linear quadrupole ion trap

Year:  2019        PMID: 31392701     DOI: 10.1007/s13361-019-02284-6

Source DB:  PubMed          Journal:  J Am Soc Mass Spectrom        ISSN: 1044-0305            Impact factor:   3.109


  7 in total

1.  Carbon disulfide reagent allows the characterization of nonpolar analytes by atmospheric pressure chemical ionization mass spectrometry.

Authors:  Benjamin C Owen; Jinshan Gao; David J Borton; Lucas M Amundson; Enada F Archibold; Xiaoli Tan; Khalid Azyat; Rik Tykwinski; Murray Gray; Hilkka I Kenttämaa
Journal:  Rapid Commun Mass Spectrom       Date:  2011-07-30       Impact factor: 2.419

2.  Comparison of Atmospheric Pressure Chemical Ionization and Field Ionization Mass Spectrometry for the Analysis of Large Saturated Hydrocarbons.

Authors:  Chunfen Jin; Jyrki Viidanoja; Mingzhe Li; Yuyang Zhang; Elias Ikonen; Andrew Root; Mark Romanczyk; Jeremy Manheim; Eric Dziekonski; Hilkka I Kenttämaa
Journal:  Anal Chem       Date:  2016-10-12       Impact factor: 6.986

3.  How to improve estimates of imprecision.

Authors:  J S Krouwer; R Rabinowitz
Journal:  Clin Chem       Date:  1984-02       Impact factor: 8.327

4.  Analysis of base oil fractions by ClMn(H2O)+ chemical ionization combined with laser-induced acoustic desorption/fourier transform ion cyclotron resonance mass spectrometry.

Authors:  Penggao Duan; Kuangnan Qian; Steven C Habicht; David S Pinkston; Mingkun Fu; Hilkka I Kenttämaa
Journal:  Anal Chem       Date:  2008-02-22       Impact factor: 6.986

5.  Atmospheric pressure chemical ionization of alkanes, alkenes, and cycloalkanes.

Authors:  S E Bell; R G Ewing; G A Eiceman; Z Karpas
Journal:  J Am Soc Mass Spectrom       Date:  1994-03       Impact factor: 3.109

6.  High molecular weight non-polar hydrocarbons as pure model substances and in motor oil samples can be ionized without fragmentation by atmospheric pressure chemical ionization mass spectrometry.

Authors:  Nadim Hourani; Nikolai Kuhnert
Journal:  Rapid Commun Mass Spectrom       Date:  2012-10-15       Impact factor: 2.419

7.  A mass spectrometry study of alkanes in air plasma at atmospheric pressure.

Authors:  Ester Marotta; Cristina Paradisi
Journal:  J Am Soc Mass Spectrom       Date:  2008-12-13       Impact factor: 3.109

  7 in total

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