2015
DOI: 10.1016/j.fuel.2015.08.038
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The oxidative stability of synthetic fuels and fuel blends with monoaromatic blending components

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Cited by 11 publications
(5 citation statements)
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“…Refer to Table for fuel identification. Errors for the stability techniques have been determined in previous work. , …”
Section: Resultsmentioning
confidence: 99%
See 1 more Smart Citation
“…Refer to Table for fuel identification. Errors for the stability techniques have been determined in previous work. , …”
Section: Resultsmentioning
confidence: 99%
“…Two separate techniques were used to assess the oxidative stability of the neat fuels. These were both static, isothermal, oxygen headspace methods that have been previously demonstrated to be a measure of the oxidative stability of middle distillate fuels. The neat fuel samples were subjected to oxidative stability testing, in order to quantitatively assess the stability of the fuels.…”
Section: Experimental Sectionmentioning
confidence: 99%
“…Aromatics generally exhibit a higher oxidative stability than cyclo-paraffins and paraffins. For example, certain monoaromatics (1,3,5-trimethylbenzene) benefit the oxidative stability of synthetic fuels [121]; the addition of diaromatics can significantly improve the oxidative stability of HEFA [109]. From Fig.…”
Section: Oxidative Stabilitymentioning
confidence: 99%
“…The branching effect on a hydrocarbon core, such as carbon chain length and carbon type, influences the oxidation stability characteristic, where the oxidation stability reduces with the carbon chain length, and the carbon type, where quaternary carbon > primary carbon > secondary carbon > tertiary carbon. , The worst oxidation stability of the tertiary carbon is due to the weaker C–H bond dissociation energy favoring hydrogen abstraction reactions, and the quaternary carbon is the most stable on which there is no more hydrogen atom to abstract . In order to minimize the tendency of oxidation, a molecular structure with more quaternary carbons and less tertiary carbons should be designed, e.g.…”
Section: Introductionmentioning
confidence: 99%
“…14,15 The worst oxidation stability of the tertiary carbon is due to the weaker C−H bond dissociation energy favoring hydrogen abstraction reactions, and the quaternary carbon is the most stable on which there is no more hydrogen atom to abstract. 16 In order to minimize the tendency of oxidation, a molecular structure with more quaternary carbons and less tertiary carbons should be designed, e.g., a fuel molecule with methyl substituents on the tertiary carbons of the polycyclic hydrocarbon core is expected to possess high oxidation stability.…”
Section: Introductionmentioning
confidence: 99%