Limits of identification using VUV spectroscopy applied to C8H18 isomers isolated by GC×GC.

The vacuum ultraviolet detector for gas chromatography can be used to identify structural differences between isomers with similar chromatographic elution times, which adds detail to characterization, valuable for prescreening of sustainable aviation fuel candidates. Although this capability has been introduced elsewhere, vacuum ultraviolet spectroscopy for saturated hydrocarbons has been examined minimally, as the similarities between their spectra are much less significant than their aromatic counterparts. The fidelity with which structural differences can be identified has been unclear. In this work, all possible structural isomers of C8H18 are measured and determined to have unambiguously unique vacuum ultraviolet spectra. Using a statistically based residual comparison approach, the concentration limits at which the spectral differences are interpretable are tested in both a controlled study and a real fuel application. The concentration limit at which the spectral differences between C8H18 isomers are unambiguous is below 0.40% by mass and less than 0.20% with human discretion in our experimental configuration.

A Data Set Comparison Method Using Noise Statistics Applied to VUV Spectrum Match Determinations.

It has been demonstrated that a pair of spectra exhibiting a coefficient of determination (R2) as low as 0.976 can originate from the same chemical species in one example, while a different pair of spectra exhibiting an R2 up to 0.9997 can originate from different chemical species. The R2 between spectra overlays depends on the signal-to-noise ratio, while the residual between any two spectra should look like noise only when the two spectra originate from the same chemical species. Numerical characteristics of the residual between two high-resolution spectra are invaluable toward the definitive elimination of many plausible matches of reference spectra to the sample spectra of analytes eluted from two-dimensional gas chromatography. Additionally, numerical characteristics beyond R2 facilitate a logical ranking of all plausible matches, making positive identification of a single-component analyte possible provided a reference spectrum exists for all plausible matches. Specifically, the experimental background noise is shown to follow a Gaussian distribution at all wavelengths, and a method is described to normalize the data such that the numerically adjusted noise distributions are independent of wavelength. The differences between matching spectra are further shown to exhibit numerical characteristics consistent with the background noise's Gaussian distribution, common to all wavelengths. Seven criteria are described for judging the similarity between spectra: R2 between the two spectra, R2 of a Q-Q plot with one axis being ideal Gaussian quantiles and the other axis being the distribution of the numerically adjusted residual quantiles, the maximum count of consecutive (by wavelength) signs in the residual, and the first four moments of the residuals. One exemplar application of the methodology is a definitive match of n-undecane, n-dodecane, and n-tridecane sample spectra to their corresponding reference spectrum, which is among the most challenging set of species within the volatility range of jet fuel to differentiate by spectral methods. While this example is a significant stress test of the approach, the utility of the methodology generally is in the subtle math and transparent criteria that unambiguously identify mismatches because the distributions of residuals between mismatching spectra are very clearly not Gaussian and have a high consecutive sign count, even in cases where the R2 between the compared spectra is ambiguous.

Toward net-zero sustainable aviation fuel with wet waste-derived volatile fatty acids.

With the increasing demand for net-zero sustainable aviation fuels (SAF), new conversion technologies are needed to process waste feedstocks and meet carbon reduction and cost targets. Wet waste is a low-cost, prevalent feedstock with the energy potential to displace over 20% of US jet fuel consumption; however, its complexity and high moisture typically relegates its use to methane production from anaerobic digestion. To overcome this, methanogenesis can be arrested during fermentation to instead produce C2 to C8 volatile fatty acids (VFA) for catalytic upgrading to SAF. Here, we evaluate the catalytic conversion of food waste-derived VFAs to produce n-paraffin SAF for near-term use as a 10 vol% blend for ASTM "Fast Track" qualification and produce a highly branched, isoparaffin VFA-SAF to increase the renewable blend limit. VFA ketonization models assessed the carbon chain length distributions suitable for each VFA-SAF conversion pathway, and food waste-derived VFA ketonization was demonstrated for >100 h of time on stream at approximately theoretical yield. Fuel property blending models and experimental testing determined normal paraffin VFA-SAF meets 10 vol% fuel specifications for "Fast Track." Synergistic blending with isoparaffin VFA-SAF increased the blend limit to 70 vol% by addressing flashpoint and viscosity constraints, with sooting 34% lower than fossil jet. Techno-economic analysis evaluated the major catalytic process cost-drivers, determining the minimum fuel selling price as a function of VFA production costs. Life cycle analysis determined that if food waste is diverted from landfills to avoid methane emissions, VFA-SAF could enable up to 165% reduction in greenhouse gas emissions relative to fossil jet.

Simultaneous measurements of refractive index, surface tension, and evaporation rate of Jet A fuel.

Simultaneous measurements of refractive index, surface tension, and evaporation rate in pendant droplets have been conducted in water, ethanol, n-heptane, diesel, and Jet A fuel in a temperature range of 20°C-50°C at atmospheric pressure. The dispersion of the refractive indices has been determined by means of rainbow refractometry. The surface tensions have been measured based on the pendant droplet shape analysis. The Young-Laplace equation and the numerical model have been applied to precisely obtain surface tension from the balance between the droplet distortion of gravity and restoring the force of surface tension. The evaporation of the fuels has also been studied with pure droplets of a few millimeters in diameter in a temperature-controlled environment. The shadowgraph technique has been performed for the precise measurement of the droplet size change with a long-working-distance objective (10× magnification). The evaporation rate has been determined by the temporal rate of droplet diameter change extracted from the subsequent images. The experimental data in this work is compared with the previous work to validate the accuracy and estimate uncertainty. Furthermore, the simultaneous multi-property measurement of Jet A fuel (POSF 4658) has been conducted. These properties of the aviation fuel can be used in computation and modeling to further improve the knowledge of jet injection (atomization and evaporation) and practical combustion processes.

Dehydration rate measurements for tertiary-butanol in a variable pressure flow reactor.

Fundamentally, the dehydration reaction of tertiary-butanol is frequently used as an internal standard for relative rate studies of other decomposition reactions. We report here a study using radical trappers to isolate this path in tertiary-butanol pyrolysis experiments conducted in the Princeton variable pressure flow reactor between 658 and 980 K. A novel technique that determines the rate constant value by applying a global least-squares fit incorporating all experimental species (tertiary-butanol, isobutene, and water) evolution data is developed and applied to yield six rate constant values at two reaction pressures (6.1 and 18 atm) and at temperatures between 949 and 980 K. Data from previously reported studies are reanalyzed to evaluate their "absolute" uncertainties, and new Arrhenius parameters are derived based upon the present and previous measurements. The recommended rate constant (uncertainties) for the dehydration reaction is k = 2.88(0.91) × 10(7)T(2.21(0.10)) s(-1) exp(-62.4(0.9) kcal mol(-1)/RT). The new correlation is in excellent agreement with other independent experimental and theoretical studies appearing in the literature.

Uncertainty analysis in the use of chemical thermometry: a case study with cyclohexene.

A general method to evaluate the absolute uncertainties in temperatures derived using chemical thermometry is developed and applied to the retro Diels-Alder reaction of cyclohexene. Experiments from previous studies of this reaction are reanalyzed to establish the minimum absolute uncertainty limit. Chemical thermometry results are compared with thermocouple measurements in experiments performed in a flow reactor at 6.1 atm pressure and at temperatures from 957 to 978 K . Using conservative uncertainty estimates, our analysis yields absolute (1σ) uncertainties of temperature through chemical thermometry using this reaction greater than ±20 at 1000 K. Neither more refined experimental techniques nor computational theory is likely to refine rate correlation parameters sufficiently to reach the absolute temperature uncertainties often reported in the literature for chemical thermometry using the retro Diels-Alder reaction of cyclohexene. Published chemical thermometry uncertainty estimates typically have not quantitatively considered the absolute uncertainties of the original data from which the reference rate correlations were based.