51 research outputs found
Oxidation Kinetics of Pure and Blended Methyl Octanoate/n-Nonane/Methylcyclohexane: Measurements and Modeling of OH*/CH* Chemiluminescence, Ignition Delay Times and Laminar Flame Speeds
The focus of the present work is on the empirical characterization and modeling of ignition trends of ternary blends of three distinct hydrocarbon classes, namely a methyl ester (C9H18O2), a linear alkane (n-C9H20), and a cycloalkane (MCH). Numerous surrogate biofuel formulations have been proposed in the literature, yet specific blending of these species has not been studied. Moreover, the effects of blending biofuel compounds with conventional hydrocarbons are not widely studied and a further point is the lack of studies paying specific attention to the effects of fuel variation within a given blended biofuel. To this end, a statistical Design of Experiments L9 array, comprised of 4 parameters (%MO, %MCH, pressure, and equivalence ratio) with 3 levels of variation, constructed in order to systematically study the effects of relative fuel concentrations within the ternary blend enabled variations in fuel concentration for methyl octanoate and MCH of 10% - 30% and 20% - 40%, respectively. Variation in pressure of 1 atm, 5 atm, and 10 atm and in equivalence ratio of 0.5, 1.0, and 2.0 were used, respectively. The fuel-volume percentage of n-nonane varied from 30% - 70%. In total, 10 ternary blends were studied.
Ignition delay times for the ternary blends and for the three constituents were obtained by monitoring excited-state OH or CH transitions, A2Epsilon+ -> X2Pi or A2Delta -> X2Pi, respectively, behind reflected shock waves using a heated shock tube facility. Dilute conditions of 99% Ar (vol.) were maintained in all shock tube experiments with the exception of a separate series of n-nonane and MCH experiments under stoichiometric conditions which used 4% oxygen (corresponding to ~ 95% Ar dilution). Temperatures behind reflected shock waves were varied over the range 1243 < T (K) < 1672. From over 450 shock tube experiments, empirical ignition delay time correlations were constructed for all three pure fuels and a master correlation equation for the blended fuels. Ignition experiments conducted on the pure fuels at 1.5 atm indicated the following ignition delay time order, from shortest to longest: methyl octanoate < n-nonane < MCH. With increased pressure to 10 atm (nominal) the order remained, in general, consistent. Under fuel-lean conditions, ignition trends between methyl octanoate and n-nonane exhibited overlap at temperatures below 1350 K, below which the trends diverged with methyl octanoate having shorter ignition delay times. Similar behavior was observed under fuel-rich conditions, yet with the overlap occurring above 1450 K. Stoichiometric ignition trends did not display overlapping behavior under either 1.5 atm or 10 atm pressure. Laminar flame speed measurements were performed at 1 atm and an initial temperature of 443 K on the pure fuel constituents. Additional flame speed measurements of MCH were conducted at 403 K to compare with literature values and were shown to agree strongly with experiments conducted in a constant-volume apparatus. The experiments conducted herein, for the first time, measure laminar flame speeds methyl octanoate.
A detailed chemical kinetics mechanism was compiled from three independent, well-validated models for the constituent fuels, where the sub-mechanisms for methyl octanoate and MCH were extracted for integration into a base n-nonane model. The compiled mechanism in the present study (4785 reactions and 1082 species) enables modeling of oxidation processes of the ternary fuel blends of interest. Calculations were performed using the compiled model relative to the base models to assess the impact of utilizing different base chemistry sets. In general, results were reproduced well relative to base models for both n-nonane and MCH, however results for methyl octanoate from both the compiled model and the base model are in disagreement with the results measured herein. Ignition delay times of the fuel blends are well-predicted for several conditions, specifically for blends at lean/high-pressure and stoichiometric/high-pressure conditions, however are not accurately modeled at fuel-rich, high-pressure conditions
Chemiluminescence and Ignition Delay Time Measurements of C9H20 Oxidation in O2-Ar Behind Reflected Shock Waves
Stemming from a continuing demand for fuel surrogates, composed of only a few species, combustion of high-molecular-weight hydrocarbons (>C5) is of scientific interest due to their abundance in petroleum-based fuels, which contain hundreds of different hydrocarbon species, used for military, aviation, and transportation applications. Fuel surrogate development involves the use of a few hydrocarbon species to replicate the physical, chemical, combustion, and ignition properties of multi-component petroleum-based fuels, enabling fundamental studies to be performed in a more controlled manner. Of particular interest are straight-chained, saturated hydrocarbons (n-alkanes) due to the high concentration of these species in diesel and jet fuels. Prior to integrating a particular hydrocarbon into a surrogate fuel formulation, its individual properties are to be precisely known. n-Nonane (n-C9H20) is found in diesel and aviation fuels, and its combustion properties have received only minimal consideration.
The present work involves first measurements of n-C9H20 oxidation in oxygen (O2) and argon (Ar), which were performed under dilute conditions at three levels of equivalence ratio (phi = 0.5, 1.0, and 2.0) and fixed pressure near 1.5 atm using a shock tube. Utilizing shock waves, high-temperature, fixed-pressure conditions are created within which the fuel reacts, where temperature and pressure are calculated using 1D shock theory and measurement of shock velocity. Of interest were measurements of ignition times and species time-histories of the hydroxyl (OH*) radical intermediate.
A salient pre-ignition feature was observed in fuel-lean, stoichiometric, and fuel-rich OH* species profiles. The feature at each equivalence ratio was observed above 1400 K with the time-of-initiation (post reflected-shock) showing dependence on phi as the initiation time shortened with increasing phi. Relative percentage calculations reveal that the fuel-rich condition produces the largest quantity of pre-ignition OH*. Ignition delay time measurements and corresponding activation energy calculations show that the phi = 1.0 mixture was the most reactive, while the phi = 0.5 condition was least reactive
Experimental and computational studies of Criegee Intermediate Reactions with NH<sub>3</sub> and CH<sub>3</sub>NH<sub>2</sub>
Direct kinetics study of CH2OO + methyl vinyl ketone and CH2OO + methacrolein reactions and an upper limit determination for CH2OO + CO reaction
Methyl vinyl ketone (MVK) and methacrolein (MACR) are important intermediate products in atmospheric degradation of volatile organic compounds, especially of isoprene. This work investigates the reactions of the smallest Criegee intermediate, CH2OO, with its co-products from isoprene ozonolysis, MVK and MACR, using multiplexed photoionization mass spectrometry (MPIMS), with either tunable synchrotron radiation from the Advanced Light Source or Lyman-alpha (10.2 eV) radiation for photoionization. CH2OO was produced via pulsed laser photolysis of CH(2)l(2) in the presence of excess O-2. Time-resolved measurements of reactant disappearance and of product formation were performed to monitor reaction progress; first order rate coefficients were obtained from exponential fits to the CH2OO decays. The bimolecular reaction rate coefficients at 300 K and 4 Torr are k(CH2OO + MVK) = (5.0 +/- 0.4) x 10(-13) cm(3) s(-1) and k(CH2OO + MACR) = (4.4 +/- 1.0) x 10(-13) cm(3) s(-1), where the stated +/- 2 sigma uncertainties are statistical uncertainties. Adduct formation is observed for both reactions and is attributed to the formation of a secondary ozonides (1,2,4-trioxolanes), supported by master equation calculations of the kinetics and the agreement between measured and calculated adiabatic ionization energies. Kinetics measurements were also performed for a possible bimolecular CH2OO + CO reaction and for the reaction of CH2OO with CF3CHCH2 at 300 K and 4 Torr. For CH2OO + CO, no reaction is observed and an upper limit is determined: k(CH2OO + CO) <2 x 10(-16) cm(3) s(-1). For CH2OO + CF3CHCH2, an upper limit of k(CH2OO + CF3CHCH2) <2 x 10(-14) cm(3) s(-1) is obtained.Peer reviewe
Direct Measurements of Unimolecular and Bimolecular Reaction Kinetics of the Criegee Intermediate (CH 3 ) 2 COO
The Criegee intermediate acetone oxide, (CH3)2COO, is formed by laser photolysis of 2,2-diiodopropane in the presence of O2 and characterized by synchrotron photoionization mass spectrometry and by cavity ring-down ultraviolet absorption spectroscopy. The rate coefficient of the reaction of the Criegee intermediate with SO2 was measured using photoionization mass spectrometry and pseudo-first-order methods to be (7.3 ± 0.5) Ă 10â11 cm3 sâ1 at 298 K and 4 Torr and (1.5 ± 0.5) Ă 10â10 cm3 sâ1 at 298 K and 10 Torr (He buffer). These values are similar to directly measured rate coefficients of anti-CH3CHOO with SO2, and in good agreement with recent UV absorption measurements. The measurement of this reaction at 293 K and slightly higher pressures (between 10 and 100 Torr) in N2 from cavity ring-down decay of the ultraviolet absorption of (CH3)2COO yielded even larger rate coefficients, in the range (1.84 ± 0.12) Ă 10â10 to (2.29 ± 0.08) Ă 10â10 cm3 sâ1. Photoionization mass spectrometry measurements with deuterated acetone oxide at 4 Torr show an inverse deuterium kinetic isotope effect, kH/kD = (0.53 ± 0.06), for reactions with SO2, which may be consistent with recent suggestions that the formation of an association complex affects the rate coefficient. The reaction of (CD3)2COO with NO2 has a rate coefficient at 298 K and 4 Torr of (2.1 ± 0.5) Ă 10â12 cm3 sâ1 (measured with photoionization mass spectrometry), again similar to rate for the reaction of anti-CH3CHOO with NO2. Cavity ring-down measurements of the acetone oxide removal without added reagents display a combination of first- and second-order decay kinetics, which can be deconvolved to derive values for both the self-reaction of (CH3)2COO and its unimolecular thermal decay. The inferred unimolecular decay rate coefficient at 293 K, (305 ± 70) sâ1, is similar to determinations from ozonolysis. The present measurements confirm the large rate coefficient for reaction of (CH3)2COO with SO2 and the small rate coefficient for its reaction with water. Product measurements of the reactions of (CH3)2COO with NO2 and with SO2 suggest that these reactions may facilitate isomerization to 2-hydroperoxypropene, possibly by subsequent reactions of association products
Products of Criegee intermediate reactions with NO2::experimental measurements and tropospheric implications
The reactions of Criegee intermediates with NO2 have been proposed as a potentially significant source of the important nighttime oxidant NO3, particularly in urban environments where concentrations of ozone, alkenes and NOx are high. However, previous efforts to characterize the yield of NO3 from these reactions have been inconclusive, with many studies failing to detect NO3. In the present work, the reactions of formaldehyde oxide (CH2OO) and acetaldehyde oxide (CH3CHOO) with NO2 are revisited to further explore the product formation over a pressure range of 4â40 Torr. NO3 is not observed; however, temporally resolved and [NO2]-dependent signal is observed at the mass of the CriegeeâNO2 adduct for both formaldehyde- and acetaldehyde-oxide systems, and the structure of this adduct is explored through ab initio calculations. The atmospheric implications of the title reaction are investigated through global modelling.</p
Release of Spring 2013 Spanish-Language MCAS Test Items
Trace atmospheric concentrations
of carboxylic acids have a potent
effect upon the environment, where they modulate aqueous chemistry
and perturb Earthâs radiative balance. Halogenated carboxylic
acids are produced by the tropospheric oxidation of halocarbons and
are considered persistent pollutants because of their weak tropospheric
and aqueous sinks. However, recent studies reported rapid reactions
between selected carboxylic acids and Criegee intermediates, which
may provide an efficient gas-phase removal process. Accordingly, absolute
rate coefficients of two Criegee intermediates, CH<sub>2</sub>OO and
(CH<sub>3</sub>)<sub>2</sub>COO, with a suite of carboxylic acids
(HCOOH, CH<sub>3</sub>COOH, CClF<sub>2</sub>COOH, CF<sub>3</sub>CF<sub>2</sub>COOH, and pyruvic acid) were measured with a view to develop
a structureâactivity relationship (SAR). This SAR is based
upon the dipole-capture model and predicts the reactivity of many
further combinations of Criegee intermediates and carboxylic acids.
Complementary synchrotron-based photoionization mass spectrometry
measurements demonstrate that these reactions produce stable ester
adducts, with a reaction coordinate involving transfer of the acidic
hydrogen from the carboxylic acid to the terminal oxygen of the Criegee
intermediate. The adduct products are predicted to have low vapor
pressures, and coupling of this chemistry with a global atmospheric
chemistry and transport model shows significant production of secondary
organic aerosol at locations rich in biogenic alkene emissions
Chemical kinetics modeling of n-nonane oxidation in oxygen/argon using excited-state species time histories
International audienc
Shock-Tube Combustion Studies Of Atomized Fuels In The Reflected-Shock Region
A liquid-spray injection system has been implemented at the University of Central Florida Gas Dynamics Laboratory to study fundamental combustion phenomena including ignition delay time measurements, soot production, and activation energies of petroleum-based and synthetic hydrocarbon fuels. The current approach uses a finely atomized jet of fuel that is injected from the endwall of a shock tube. The micron-scale fuel droplets are heated and combusted behind the reflected shock wave at elevated temperatures. Repeatability and initial characterization of the electronically controlled, autonomous system has been performed using ignition delay time measurements of kerosene droplets over consistent temperature (1260 K) and pressure (1.4 atm) conditions behind the reflected shock. Details on the first phase of the design and implementation of the technique are provided along with ignition delay time measurements of kerosene at low pressures
Effect Of Ceria Nanoparticles On Soot Inception And Growth In Toluene-Oxygen-Argon Mixtures
Soot formation from the combustion of toluene (C6H 5CH3) and of two concentrations of nano-sizedceria-laden toluene was monitored using a shock tube to observe the effect of the organometallic additive on the formation of soot from its point of inception. Two concentrations of ceria, of chemical composition CeO1.63, were employed to examine the effect on soot production of toluene over the range of temperature 1588-2370 K using two levels of inert gas dilution in which reflected-shock pressure was maintained near 1.5 atm. The ceria nanoparticles were synthesized using a microemulsion technique which employs sodium dioctyl sulfosuccmate (AOT), a surfactant, to retard agglomeration. Introduction of the nanoparticles into the shock tube is achieved using a novel, two-stage injection procedure. Soot yield measurements reveal that the presence of ceria has no direct implications on peak soot concentration near 1950 K. A shift in the parabolic soot profile of toluene in the direction of increased temperature was observed for each concentration of ceria with a larger shift occurring for increased concentration of ceria, although the same effect was exhibited for the toluene-AOT mixtures in absence of ceria, supporting an inefficaciousness of ceria on soot suppression on kinetic timescales. It is evidenced in measured soot delay times that the presence of the surfactant in absence of ceria significantly slows the rate of soot growth for T \u3c 2000 K, while the presence of ceria has a relatively negligible impact. Under conditions of higher fuel concentration, a remarkable decrease in soot accumulation on the shock tube walls was observed in experiments using the ceria-toluene mixtures over that yielded by pure toluene combustion. In the present paper, the authors report the first measurements of nanoparticle-influenced combustion of a hydrocarbon as performed in a shock tube. © 2009 The Combustion Institute. Published by Elsevier Inc. All rights reserved
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