Tina Kasper

Biofuel Combustion Chemistry: From Ethanol to Biodiesel

Biofuels, such as bio-ethanol, bio-butanol, and biodiesel, are of increasing interest as alternatives to petroleum-based transportation fuels because they offer the long-term promise of fuel-source regenerability and reduced climatic impact. Current discussions emphasize the processes to make such alternative fuels and fuel additives, the compatibility of these substances with current fuel-delivery infrastructure and engine performance, and the competition between biofuel and food production. However, the combustion chemistry of the compounds that constitute typical biofuels, including alcohols, ethers, and esters, has not received similar public attention. Herein we highlight some characteristic aspects of the chemical pathways in the combustion of prototypical representatives of potential biofuels. The discussion focuses on the decomposition and oxidation mechanisms and the formation of undesired, harmful, or toxic emissions, with an emphasis on transportation fuels. New insights into the vastly diverse and complex chemical reaction networks of biofuel combustion are enabled by recent experimental investigations and complementary combustion modeling. Understanding key elements of this chemistry is an important step towards the intelligent selection of next-generation alternative fuels.

Sampling Probe Influences on Temperature and Species Concentrations in Molecular Beam Mass Spectroscopic Investigations of Flat Premixed Low-pressure Flames

Abstract New operating regimes for engines and combustors and the advocated use of non-conventional transportation fuels demand investigation of the combustion chemistry of different classes of chemicals, especially under premixed conditions. Detailed species compositions during combustion are needed to estimate hazardous emissions, and models for their prediction must be validated for the intended combustion conditions.Molecular-beam mass spectrometry (MBMS) is a common technique to measure quantitative species concentrations in flames. It is widely employed to characterize the flame chemistry of laminar premixed combustion, and it has been complemented with optical measurements for the detection of a number of molecular species and radicals. Significant progress has been made in recent studies through the introduction of synchrotron-based MBMS instruments. They have improved the identification process by using tunable vacuum-ultraviolet radiation for photoionization of the species to be detected, and isomer-specific measurements are now almost routinely possible. Along with quantitative species measurements, the temperature profile is needed as input parameter for chemical kinetic modeling. It is usually determined either using thermocouples or laser spectroscopic techniques.It is an ongoing discussion how sampling probes affect these measurements, and how MBMS results can be compared to combustion modeling. The present article is intended to contribute to this discussion by providing optical and MBMS results obtained with several sampling configurations.

Isomer-specific influences on the composition of reaction intermediates in dimethyl ether/propene and ethanol/propene flame.

This work provides experimental evidence on how the molecular compositions of fuel-rich low-pressure premixed flames are influenced as the oxygenates dimethyl ether (DME) or ethanol are incrementally blended into the propene fuel. Ten different flames with a carbon-to-oxygen ratio of 0.5, ranging from 100% propene (phi = 1.5) to 100% oxygenated fuel (phi = 2.0), are analyzed with flame-sampling molecular-beam mass spectrometry employing electron- or photoionization. Absolute mole fraction profiles for flame species with masses ranging from m/z = 2 (H2) to m/z = 80 (C6H8) are analyzed with particular emphasis on the formation of harmful emissions. Fuel-specific destruction pathways, likely to be initiated by hydrogen abstraction, appear to lead to benzene from propene combustion and to formaldehyde and acetaldehyde through DME and ethanol combustion, respectively. While the concentration of acetaldehyde increases 10-fold as propene is substituted by ethanol, it decreases as propene is replaced with DME. In contrast, the formaldehyde concentration rises only slightly with ethanol replacement but increases markedly with addition of DME. Allyl and propargyl radicals, the dominant precursors for benzene formation, are likely to be produced directly from propene decomposition or via allene and propyne. Benzene formation through propargyl radicals formed via unsaturated C2 intermediates in the decomposition of DME and ethanol is negligibly small. As a consequence, DME and ethanol addition lead to similar reductions of the benzene concentration.

In situ flame chemistry tracing by imaging photoelectron photoion coincidence spectroscopy

Adaptation of a low-pressure flat flame burner with a flame-sampling interface to the imaging photoelectron photoion coincidence spectrometer (iPEPICO) of the VUV beamline at the Swiss Light Source is presented. The combination of molecular-beam mass spectrometry and iPEPICO provides a new powerful analytical tool for the detailed investigation of reaction networks in flames. First results demonstrate the applicability of the new instrument to comprehensive flame diagnostics and the potentially high impact for reaction mechanism development for conventional and alternative fuels. Isomer specific identification of stable and radical flame species is demonstrated with unrivaled precision. Radical detection and identification is achieved for the initial H-abstraction products of fuel molecules as well as for the reaction controlling H, O, and OH radicals. Furthermore, quantitative evaluation of changing species concentrations during the combustion process and the applicability of respective results for kinetic model validation are demonstrated. Utilization of mass-selected threshold photoelectron spectra is shown to ensure precise signal assignment and highly reliable spatial profiles.

Identification of tetrahydrofuran reaction pathways in premixed flames

Abstract Premixed low-pressure tetrahydrofuran/oxygen/argon flames are investigated by photoionization molecular-beam mass spectrometry using vacuum-ultraviolet synchrotron radiation. For two equivalence ratios (φ = 1.00 and 1.75), mole fractions are measured as a function of distance from the burner for almost 60 intermediates with molar masses ranging from 2 (H2) to 88 (C4H6O2), providing a broad database for flame modeling studies. The isomeric composition is resolved by comparisons between experimental photoionization efficiency data and theoretical simulations, based on calculated ionization energies and Franck-Condon factors. Special emphasis is put on the resolution of the first reaction steps in the fuel destruction. The photoionization experiments are complemented by electron-ionization molecular-beam mass-spectrometry measurements that provide data with high mass resolution. For three additional flames with intermediate equivalence ratios (φ = 1.20, 1.40 and 1.60), mole fractions of major species and photoionization efficiency spectra of intermediate species are reported, extending the database for the development of chemical kinetic models.

Contributions to the investigation of reaction pathways in fuel-rich flames

Development and validation of detailed reaction mechanisms for fuel-rich combustion have a continuing need for quantitative experimental flame data. In this study, an overview is presented of recent experimental investigations of a series of fuel-rich premixed low-pressure flames burning acetylene, propene, linear and cyclic C5-alkenes and C5-alkanes with a combination of laser spectroscopy and molecular beam mass spectrometry (MBMS). Particular attention was devoted to the reaction pathways leading to the first aromatic ring. Fuel-specific aspects with respect to benzene formation are discussed. The potential of resonance-enhanced multi-photon ionisation (REMPI) MBMS as a quantitative technique for the measurement of stable species is examined for benzene as an example. Also, first results of the investigation of a fuel-rich ethanol flame under similar conditions are given. Advantages and potential drawbacks of the applied diagnostic methods are discussed in view of the importance of reliable, quantitative measurements for the understanding of fuel-rich chemistry preceding polycyclic aromatic hydrocarbon (PAH) and soot formation as well as for the related modelling of these chemical processes.

Combination of Laser- and Mass-Spectroscopic Techniques for the Investigation of Fuel-Rich Flames

Abstract Soot is one of the most important pollutants originating from combustion. Despite recent advances in the measurement of size and composition of soot particles, their actual formation mechanism is still under debate. It depends on fuel, stoichiometry, temperature, flow conditions and the concentration of a large number of intermediate species. An adequate characterization of this complex reaction system generally requires the use of several complementary techniques. In this article, we present measurements aiming to study reactions in fuel-rich flames using several complementary techniques. Only with a combination of optical and mass-spectrometric measurements, important features of the early polyaromatic hydrocarbon (PAH) and soot formation chemistry are accessible in detail. Three different techniques are combined to investigate one-dimensional laboratory flames on the same low-pressure burner and their respective merits are discussed: (i) cavity ring-down spectroscopy (CRDS) for the detection of small radicals and measurement of the temperature, (ii) mass spectrometry with electron-impact (EI) ionization in order to measure species with molecular weights up to m/e = 90, and (iii) mass spectrometry with resonantly-enhanced multi-photon ionization (REMPI) to distinguish isomers with masses up to m/e = 178. Measurements of this type may prove a valuable input to improve kinetic and combustion models.

Noncatalytic thermocouple coatings produced with chemical vapor deposition for flame temperature measurements.

Chemical vapor deposition (CVD) and metal-organic chemical vapor deposition (MOCVD) have been employed to develop alumina thin films in order to protect thermocouples from catalytic overheating in flames and to minimize the intrusion presented to the combustion process. Alumina films obtained with a CVD process using AlCl(3) as the precursor are dense, not contaminated, and crystallize in the corundum structure, while MOCVD using Al(acetyl acetone)(3) allows the growth of corundum alumina with improved growth rates. These films, however, present a porous columnar structure and show some carbon contamination. Therefore, coated thermocouples using AlCl(3)-CVD were judged more suitable for flame temperature measurements and were tested in different fuels over a typical range of stoichiometries. Coated thermocouples exhibit satisfactory measurement reproducibility, no temporal drifts, and do not suffer from catalytic effects. Furthermore, their increased radiative heat loss (observed by infrared spectroscopy) allows temperature measurements over a wider range when compared to uncoated thermocouples. A flame with a well-known temperature profile established with laser-based techniques was used to determine the radiative heat loss correction to account for the difference between the apparent temperature measured by the coated thermocouple and the true flame temperature. The validity of the correction term was confirmed with temperature profile measurements for several flames previously studied in different laboratories with laser-based techniques.

Buoyancy induced limits for nanoparticle synthesis experiments in horizontal premixed low-pressure flat-flame reactors

Premixed low-pressure flat-flame reactors can be used to investigate the synthesis of nanoparticles. The present work examines the flow field inside such a reactor during the formation of carbon (soot) and iron oxide (from Fe(CO)5) nanoparticles, and how it affects the measurements of nanoparticle size distribution. The symmetry of the flow and the impact of buoyancy were analysed by three-dimensional simulations and the nanoparticle size distribution was obtained by particle mass spectrometry (PMS) via molecular beam sampling at different distances from the burner. The PMS measurements showed a striking, sudden increase in particle size at a critical distance from the burner, which could be explained by the flow field predicted in the simulations. The simulation results illustrate different fluid mechanical phenomena which have caused this sudden rise in the measured particle growth. Up to the critical distance, buoyancy does not affect the flow, and an (almost) linear growth is observed in the PMS experiments. Downstream of this critical distance, buoyancy deflects the hot gas stream and leads to an asymmetric flow field with strong recirculation. These recirculation zones increase the particle residence time, inducing very large particle sizes as measured by PMS. This deviation from the assumed symmetric, one-dimensional flow field prevents the correct interpretation of the PMS results. To overcome this problem, modifications to the reactor were investigated; their suitability to reduce the flow asymmetry was analysed. Furthermore, ‘safe’ operating conditions were identified for which accurate measurements are feasible in premixed low-pressure flat-flame reactors that are transferrable to other experiments in this type of reactor. The present work supports experimentalists to find the best setup and operating conditions for their purpose.

Partial Oxidation of Methane at Elevated Pressures and Effects of Propene and Ethane as Additive: Experiment and Simulation

Abstract Partial homogeneous oxidation of methane (CH4) within stationary engines may be one concept for conversion of available energy to alternatively mechanical energy, heat, and additional useful chemicals like syngas (CO/H2), formaldehyde (CH2O), methanol (CH3OH) or hydrocarbons (e.g. C2H4). The present study investigates the formation reactions of chemicals experimentally and theoretically. Methane oxidation is studied under fuel-rich conditions (ϕ = 17.50–22.25) at high pressures (6 bar) and high temperatures (T  max  = 1030 K) for long residence times in a tubular reactor. The gas composition is determined experimentally by time-of-flight mass spectrometry for different reactor temperatures. Through variation of reactor temperature an overview of the maximum mole fractions of target chemicals, the temperature of observed reaction onset, and the optimal temperature to increase target yields can be determined. The experimental results are compared to kinetic simulations of the methane conversion using literature mechanisms to assess how well the data are reproduced for these uncommon reaction conditions. The potential of activating the conversion reactions with ethane (C2H6) and propene (C3H6) as additives is investigated. Methanol is chosen as one target compound. Its yield is increased by both additives. In addition, propene as additive reduces the temperature of reaction onset in the experiments and in the simulation. CH2O and C2H4 can be identified as other useful chemicals produced in the experiments and the influence of the additives on the yields is discussed.