Influence of Biodiesel on Base Oil Oxidation as Measured by FTICR Mass Spectrometry

被引:14
作者
Jones, Hugh E. [1 ,2 ]
Lozano, Diana Catalina Palacio [2 ]
Huener, Chris [3 ]
Thomas, Mary J. [1 ,2 ]
Aaserud, David J. [4 ]
DeMuth, J. Corinne [4 ]
Robin, Mathew P. [3 ]
Barrow, Mark P. [2 ]
机构
[1] Univ Warwick, Mol Analyt Sci Ctr Doctoral Training, Coventry CV4 7AL, W Midlands, England
[2] Univ Warwick, Dept Chem, Coventry CV4 7AL, W Midlands, England
[3] Lubrizol Ltd, Derby DE56 4AN, England
[4] Lubrizol Corp, Wickliffe, OH 44092 USA
基金
英国工程与自然科学研究理事会;
关键词
THERMOOXIDATIVE STABILITY; ELECTROSPRAY-IONIZATION; CHROMATOGRAPHY; ANTIOXIDANTS; DEGRADATION; GENERATION; LUBRICANTS;
D O I
10.1021/acs.energyfuels.1c01240
中图分类号
TE [石油、天然气工业]; TK [能源与动力工程];
学科分类号
0807 ; 0820 ;
摘要
Internal combustion engine lubricants are subject to thermo-oxidative degradation during use and must be designed to withstand oxidation in order to extend their useful life. Understanding the complex chemical process of thermo-oxidative degradation is essential to designing higher performing engine lubricants. In this study base oil samples composed of a Group II base oil, doped with three different levels of biodiesel (B0, B15, and B100), were subjected to benchtop oxidation testing of up to 168 h, which mimics the conditions experienced in an internal combustion engine. The resulting samples were analyzed by Fourier transform ion cyclotron resonance mass spectrometry (FTICR MS) for ultrahigh-resolution characterization to monitor oxidation as a function of time and biofuel content. Both negative-ion nanoelectrospray ionization and positive-ion atmospheric pressure photoionization were utilized. Most of the oxidation products were found to be polyoxygenated species containing 1-8 oxygen atoms, with the number of detected species increasing with oxidation time. Assessment of the maximum carbon number of protonated classes indicated the involvement of oligomerization reactions; additionally, modeling of mean double bond equivalents (DBE) for each protonated class suggests increasing carbonyl content for each particular class with increasing oxidation time. The oxidations of B15 and B100 doped samples were compared to that of B0. BIS samples were found to correspond closely to B0 samples, with a similar number of species detected. B100 samples showed a significant increase in number of species generated at 24-72 h relative to B0 and B15; however, a similar number of species were observed at 168 h for all samples, indicating a similar level of base oil oxidation at the final oxidation point. FTICR MS is shown to afford new insights into base oil oxidation as a function of time and biofuel content.
引用
收藏
页码:11896 / 11908
页数:13
相关论文
共 60 条
  • [11] Rapid analysis of lubricants by atmospheric solid analysis probe-ion mobility mass spectrometry
    Barrere, Caroline
    Hubert-Roux, Marie
    Afonso, Carlos
    Racaud, Amandine
    [J]. JOURNAL OF MASS SPECTROMETRY, 2014, 49 (08): : 709 - 715
  • [12] Petroleum crude oil analysis using low-temperature plasma mass spectrometry
    Benassi, Mario
    Berisha, Arton
    Romao, Wanderson
    Babayev, Elbay
    Roempp, Andreas
    Spengler, Bernhard
    [J]. RAPID COMMUNICATIONS IN MASS SPECTROMETRY, 2013, 27 (07) : 825 - 834
  • [13] Generation of engine oils with defined degree of degradation by means of a large scale artificial alteration method
    Besser, Charlotte
    Agocs, Adam
    Ronai, Bettina
    Ristic, Andjelka
    Repka, Martin
    Jankes, Erik
    McAleese, Colin
    Doerr, Nicole
    [J]. TRIBOLOGY INTERNATIONAL, 2019, 132 : 39 - 49
  • [14] Bouillon V., 2018, TRIBOL SCHMIERUNGSTE, V65, P38
  • [15] Braun J., 2017, LUBRICANTS LUBRICATI, P88
  • [16] Composition and oxidation stability of SAE 15W-40 engine oils
    Cerny, J
    Strnad, Z
    Sebor, G
    [J]. TRIBOLOGY INTERNATIONAL, 2001, 34 (02) : 127 - 134
  • [17] Application of FT-ICR MS Equipped with Quadrupole Detection for Analysis of Crude Oil
    Cho, Eunji
    Witt, Matthias
    Hur, Manhoi
    Jung, Maeng-Joon
    Kim, Sunghwan
    [J]. ANALYTICAL CHEMISTRY, 2017, 89 (22) : 12101 - 12107
  • [18] Devlin C. C., 2008, SAE TECH PAP SER, DOI [10.4271/2008-01-2375, DOI 10.4271/2008-01-2375]
  • [19] Edmisten W. C., 1970, SAE TECHNOL PAP SER, DOI [10.4271/700509, DOI 10.4271/700509]
  • [20] Fang H. L., 2006, SAE TECH PAP SER, V724, P776