Two-wavelength mid-IR absorption diagnostic for simultaneous measurement of temperature and hydrocarbon fuel concentration

A two-wavelength mid-IR laser is used for time-resolved absorption-based measurements of temperature and n-heptane concentration in shock-heated gases. The novel difference-frequency-generation laser provides tunable mid-IR light from nonlinear conversion of near-IR light, enabling access to the strong hydrocarbon absorption bands between 3.3 and 3.5 μm associated with the CH stretching vibration. This laser was modified to alternate between two mid-IR wavelengths at 200 kHz, providing 5 μs time resolution for simultaneous monitoring of temperature and concentration in reactive flows and combustion systems. Temperature-dependent absorption spectra of n-heptane are first measured in a cell from 298 to 773 K using an FTIR spectrometer. These spectra are used to select candidate pairs of wavelengths with good sensitivity to temperature and concentration and to provide accurate temperature-dependent absorption cross-sections at the selected wavelengths. Laser absorption measurements of shock-heated n-heptane are then used to extend the cross-section data to 1300 K and to investigate the sensor accuracy and noise characteristics. The temperature and concentration inferred from the measurements are compared to known post-shock conditions, with a 4.5% RMS deviation from the calculated temperature and 1.7% RMS deviation from the calculated concentration. Finally, at high temperatures, the sensor is used to monitor decomposition of n-heptane, illustrating the potential of this diagnostic for hydrocarbon kinetics experiments in shock tubes. This new sensor concept should prove useful for simultaneous, time-resolved temperature and hydrocarbon concentration measurements in a variety of combustion and propulsion applications.     

Two-wavelength mid-IR diagnostic for temperature and n-dodecane concentration in an aerosol shock tube

A two-wavelength, mid-IR optical absorption diagnostic is developed for simultaneous temperature and n-dodecane vapor concentration measurements in an aerosol-laden shock tube. FTIR absorption spectra for the temperature range 323 to 773 K are used to select the two wavelengths (3409.0 and 3432.4 nm). Shock-heated mixtures of n-dodecane vapor in argon are then used to extend absorption cross section data at these wavelengths to 1322 K. The sensor is used to validate a model of the post-evaporation temperature and pressure of shock-heated fuel aerosol, which can ultimately be used for the study of the chemistry of low-vapor-pressure compounds and fuel blends. The signal-to-noise ratio of the temperature and concentration are ～20 and ～30, respectively, illustrating the sensitivity of this diagnostic. The good agreement between model and measurement provide confidence in the use of this aerosol shock tube to provide well-known thermodynamic conditions. At high temperatures, pseudo-first-order decomposition rates are extracted from time-resolved concentration measurements, and data from vapor and aerosol shocks are found to be in good agreement. Notably, the n-dodecane concentration measurements exhibit slower decomposition than predicted by models using two published reaction mechanisms, illustrating the need for further kinetic studies of this hydrocarbon. These results demonstrate the potential of multi-wavelength mid-IR laser sensors for hydrocarbon measurements in environments with time-varying temperature and concentration.     

Temperature-dependent mid-IR absorption spectra of gaseous hydrocarbons

Quantitative mid-IR absorption spectra (2500-3400 cm⁻¹) for 12 pure hydrocarbon compounds are measured at temperatures ranging from 25 to 500 °C using an FTIR spectrometer. The hydrocarbons studied are n-pentane, n-heptane, n-dodecane, 2,2,4-trimethyl-pentane (iso-octane), 2-methyl-butane, 2-methyl-pentane, 2,4,4-trimethyl-1-pentene, 2-methyl-2-butene, propene, toluene, m-xylene, and ethylbenzene. Room-temperature measurements of neat hydrocarbon vapor were made with an instrument resolution of both 0.1 and 1 cm⁻¹ (FWHM) to confirm that the high-resolution setting was required only to resolve the propene absorption spectrum while the spectra of the other hydrocarbons could be resolved with 1 cm⁻¹ resolution. High-resolution (0.1 cm⁻¹), room-temperature measurements of neat hydrocarbons were made at low pressure (∼1 Torr, 133 Pa) and compared to measurements of hydrocarbon/N₂ mixtures at atmospheric pressure to verify that no pressure broadening could be observed over this pressure range. The temperature was varied between 25 and 500 °C for atmospheric-pressure measurements of hydrocarbon/N₂ mixtures (X_hydrocarbon∼0.06-1.5%) and it was found that the absorption cross section shows simple temperature-dependent behavior for a fixed wavelength over this temperature range. Comparisons with previous FTIR data over a limited temperature range and with high-resolution laser absorption data over a wide temperature range show good agreement.     

n-Dodecane oxidation at high-pressures: Measurements of ignition delay times and OH concentration time-histories

Ignition delay times and OH concentration time-histories were measured during n-dodecane oxidation behind reflected shocks waves using a heated, high-pressure shock tube. Measurements were made over temperatures of 727-1422 K, pressures of 15-34 atm, and equivalence ratios of 0.5 and 1.0. Ignition delay times were measured using side-wall pressure and OH^∗ emission diagnostics, and OH concentration time-histories were measured using narrow-linewidth ring-dye laser absorption near the R-branchhead of the OH A-X (0, 0) system at 306.47 nm. Shock tube measurements were compared to model predictions of four current n-dodecane oxidation detailed mechanisms, and the differences, particularly in the low-temperature negative-temperature-coefficient (NTC) region where the influence of non-ideal facility effects can be significant, are discussed. To our knowledge, the current measurements provide the first gas-phase shock tube ignition delay times (at pressures above 13 atm) and quantitative OH concentration time-histories for n-dodecane oxidation under practical engine conditions, and hence provide benchmark validation targets for refinement of jet fuel detailed kinetic modeling, since n-dodecane is widely used as the principal representative for n-alkanes in jet fuel surrogates.     

Methyl concentration time-histories during iso-octane and n-heptane oxidation and pyrolysis

Methyl radical concentration time-histories were measured during the oxidation and pyrolysis of iso-octane and n-heptane behind reflected shock waves. Initial reflected shock conditions covered temperatures of 1100-1560 K, pressures of 1.6-2.0 atm and initial fuel concentrations of 100-500 ppm. Methyl radicals were detected using cw UV laser absorption near 216 nm; three wavelengths were used to compensate for time- and wavelength-dependent interference absorption. Methyl time-histories were compared to the predictions of several current oxidation models. While some agreement was found between modeling and measurement in the early rise, peak and plateau values of methyl, and in the ignition time, none of the current mechanisms accurately recover all of these features. Sensitivity analysis of the ignition times for both iso-octane and n-heptane showed a strong dependence on the reaction C₃H₅ + H = C₃H₄ + H₂, and a recommended rate was found for this reaction. Sensitivity analysis of the initial rate of CH₃ production during pyrolysis indicated that for both iso-octane and n-heptane, reaction rates for the initial decomposition channels are well isolated, and overall values for these rates were obtained. The present concentration time-history data provide strong constraints on the reaction mechanisms of both iso-octane and n-heptane oxidation, and in conjunction with OH concentration time-histories and ignition delay times, recently measured in our laboratory, should provide a self-consistent set of kinetic targets for the validation and refinement of iso-octane and n-heptane reaction mechanisms.     

Experiments and modeling of ignition delay times, flame structure and intermediate species of EHN-doped stoichiometric n-heptane/air combustion

The combustion of stoichiometric Ethyl-hexyl-nitrate (EHN)-doped n-heptane/oxygen/argon and (EHN)-doped n-heptane/air mixtures, respectively, was investigated in a low-pressure burner with a molecular-beam mass spectrometer and ignition delay-time (τ_ign) measurements were performed in a high-pressure shock tube. The experiments with the low-pressure flame were used for the determination of the flame structure including concentration profiles of reactants, products and important intermediates in the flame. The shock tube experiments provided τ_ign for a temperature range of 690 K ? T ? 1275 K at a pressure of 40 ± 2 bar for stoichiometric and lean mixtures under engine relevant conditions. A chemical mechanism for n-heptane/EHN mixtures was developed from an automatically generated mechanism for n-heptane by manually adding reactions to describe the influence of EHN. This mechanism was validated against the shock-tube data for various temperatures, levels of EHN-doping and equivalence ratios by homogeneous reactor calculations.The ignition delay times predicted by the model agree well with the shock tube results for a large range of temperatures, equivalence ratios and EHN concentrations. The influence of EHN onto ignition delay was largest in the low-temperature regime (770-1000 K).Numerical analysis suggests that the prevalent reason for the ignition-enhancing effect of EHN is the formation of highly reactive heptyl radicals by thermal decomposition of EHN. Due to this comparatively simple and generic mechanism, EHN is expected to have a similar ignition-enhancing effect also for other hydrocarbon fuels.     

Autoignition and combustion of hydrocarbon-hydrogen-air homogeneous and heterogeneous ternary mixtures

A numerical simulation of the ignition and combustion of hydrocarbon-hydrogen-air homogeneous and heterogeneous (gas-drop) ternary mixtures for three hydrocarbon fuels (n-heptane, n-decane, and n-dodecane) is for the first time performed. The simulation is carried out based on a fully validated detailed kinetic mechanism of the oxidation of n-dodecane, which includes the mechanisms of the oxidation of n-decane, n-heptane, and hydrogen as constituent parts. It is demonstrated that the addition of hydrogen to a homogeneous or heterogeneous hydrocarbon-air mixture increases the total ignition delay time at temperatures below 1050 K, i.e., hydrogen acts as an ignition inhibitor. At low temperatures, even ternary mixtures with a very high hydrogen concentration show multistage ignition, with the temperature dependence of the ignition delay time exhibiting a negative temperature coefficient region. Conversely, the addition of hydrogen to homogeneous and heterogeneous hydrocarbon-air mixtures at temperatures above 1050 K reduces the total ignition delay time, i.e., hydrogen acts as an autoignition promoter. These effects should be kept in mind when discussing the prospects for the practical use of hydrogen-containing fuel mixtures, as well as in solving the problems of fire and explosion safety.     

Measurements of near-UV absorption spectra of acetone and 3-pentanone at high temperatures

Gas phase acetone and 3-pentanone absorption cross sections have been measured in shock-heated gases in the wavelength range from 220 to 340 nm (the n−π^* system) at temperatures between 300 and 1100 K. Absorption measurements using a deuterium source and a kinetic spectrograph enable accurate, broadband measurements of absorption cross sections while simultaneously observing decomposition at elevated temperatures, thus minimizing errors due to product formation. The absorption spectra of both ketones increase in strength and shift to the red with increasing temperature. The spectra are fitted to a parameterized Gaussian curve to allow for calculations of the cross sections as a function of temperature and wavelength.     

Mid-infrared laser-absorption diagnostic for vapor-phase fuel mole fraction and liquid fuel film thickness

A novel two-wavelength mid-infrared laser-absorption diagnostic has been developed for simultaneous measurements of vapor-phase fuel mole fraction and liquid fuel film thickness. The diagnostic was demonstrated for time-resolved measurements of n-dodecane liquid films in the absence and presence of n-decane vapor at 25°C and 1 atm. Laser wavelengths were selected from FTIR measurements of the C–H stretching band of vapor n-decane and liquid n-dodecane near 3.4 μm (3000 cm⁻¹). n-Dodecane film thicknesses <20 μm were accurately measured in the absence of vapor, and simultaneous measurements of n-dodecane liquid film thickness and n-decane vapor mole fraction (300 ppm) were measured with <10% uncertainty for film thicknesses <10 μm. A potential application of the measurement technique is to provide accurate values of vapor mole fraction in combustion environments where strong absorption by liquid fuel or oil films on windows make conventional direct absorption measurements of the gas problematic.     

Simultaneous phosphor and CARS thermometry at the wall-gas interface within a combustor

Phosphor thermometry and vibrational coherent anti-stokes Raman spectroscopy (CARS) were applied simultaneously to examine gas-solid interfaces in a generic combustor. For this purpose, an internally air-cooled obstacle was installed within an optically accessible, pressurized combustion chamber. During the operation of a turbulent, swirled n-heptane flame, the obstacle’s surface temperature and the surface-normal gas temperature distribution were measured. The surface temperature was determined by Thermographic Phosphors, materials whose phosphorescence decay times depend on their temperature. Following a pulsed UV laser excitation (355 nm), the 659 nm emission band of Mg₄FGeO₆:Mn was monitored by a photomultiplier tube.Non-invasive temperature measurements in the flue gas region of the n-heptane spray flame near the surface were performed pointwise by vibrational CARS of diatomic nitrogen. Beams from a frequency doubled Nd:YAG laser (532 nm) and a modeless broadband dye laser (607 nm) were phase-matched within a surface-parallel, planar BOXCARS configuration. This allowed gas phase thermometry as close as 30 μm to the surface.The thermal boundary layer and wall temperature measurements were consistent with each other. This demonstrates the potential of spectrocopic techniques to study gas-solid interfaces with high temporal and spatial resolution. Using the interior surface temperature within the cooling channel measured by a thermocouple, the heat flux through the wall and the local heat transfer coefficient at the front side of the obstacle were estimated.     

A widely tunable (5-12.5 μm) continuous-wave mid-infrared laser spectrometer based on difference frequency generation in AgGaS2

A widely tunable (5-12.5 μm) continuous-wave (cw) mid-infrared (mid-IR) laser spectrometer based on difference frequency generation (DFG) by mixing an external-cavity diode laser (ECDL) with a Ti:Sapphire laser in an AgGaS₂ crystal is described. The wide tunability was achieved by tuning laser wavelength associated with crystal angle tuning under type II phase matching condition. A maximum output power of about 66 nW was obtained at 8.06 μm. High resolution spectrum of methane (CH₄) over more than 10 cm⁻¹ near 7.7 μm has been recorded to evaluate the performance of the developed DFG-based mid-IR laser spectrometer.     

Tunable and switchable dual-wavelength passively mode-locked fiber ring laser with high-energy pulses at a sub-100 kHz repetition rate

We demonstrate a tunable and switchable dual-wavelength passively mode-locked fiber ring laser in the anomalous dispersion regime that generates high-energy pulses at a sub-100 kHz repetition rate. The nonlinear polarization rotation (NPR) technique is employed in this configuration to allow for passively mode-locked operation. By exploiting the intensity-dependent loss caused by NPR, the mode competition could be efficiently alleviated. Moreover, taking advantage of the intrinsic spectral filter induced by the intracavity birefringence, the dual-wavelength separations as well as the wavelength lasing locations could be flexibly tuned by properly rotating the polarization controller. With a repetition rate of 85.8 kHz, the laser delivers the single pulse energy of 198 nJ at a pump power of 250 mW. The combination of high per-pulse energy and flexible tunability in this fiber laser is useful for practical applications.     

Switchable and tunable dual-wavelength ultrashort pulse generation in a passively mode-locked erbium-doped fiber ring laser

A simple switchable and tunable dual-wavelength passively mode-locked erbium-doped fiber ring laser based on nonlinear polarization rotation (NPR) effect is proposed and experimentally demonstrated. The NPR effect effectively induces wavelength- and intensity-dependent loss to readily implement stable dual-wavelength passively mode-locked operation. The wavelength switching and tuning of the dual-wavelength ultrashort pulse laser are achieved only by appropriately rotating the polarization controllers. The side-mode suppression ratio of the output pulse is larger than 41 dB over a wavelength-tuning range of 43.4 nm. Moreover, triple-wavelength ultrashort pulse can also be observed.     

First-time lidar measurement of water vapor flux in a volcanic plume

The CO₂ laser-based lidar ATLAS has been used to study the Stromboli volcano plume. ATLAS measured water vapor concentration in cross-sections of the plume and wind speed at the crater. Water vapor concentration and wind speed were retrieved by differential absorption lidar and correlation technique, respectively. Lidar returns were obtained up to a range of 3 km. The spatial resolution was 15 m and the temporal resolution was 20 s. By combining these measurements, the water vapor flux in the Stromboli volcano plume was found. To our knowledge, it is the first time that lidar retrieves water vapor concentrations in a volcanic plume.     

Experimental study of H2O spectroscopic parameters in the near-IR (6940-7440 cm) for gas sensing applications at elevated temperature

Tunable diode laser (TDL) absorption sensors of water vapor are attractive for temperature, gas composition, velocity, pressure, and mass flux measurements in a variety of practical applications including hydrocarbon-fueled combustion systems. Optimized design of these sensors requires a complete catalog of the assigned transitions with accurate spectroscopic data; our particular interest has been in the 2ν₁, 2ν₃, and ν₁+ν₃ bands in the near-IR where telecommunications diode lasers are available. In support of this need, fully resolved absorption spectra of H₂O vapor in the spectral range of 6940-7440 cm⁻¹ (1344-1441 nm) have been measured as a function of temperature (296-1000 K) and pressure (1-800 Torr), and quantitative spectroscopic parameters inferred from these spectra compared to published data from Toth, HITRAN 2000 and HITRAN 2004. The peak absorbances were measured for more than 100 strong transitions at 296 and 828 K, and linestrengths determined for 47 strong lines in this region. In addition to reference linestrengths S(296 K), the air-broadening coefficients γ_air(296 K) and temperature exponents n were inferred for strong transitions in five narrow regions, near 7185.60, 7203.89, 7405.11, 7426.14 and 7435.62 cm⁻¹ that had been targeted as attractive for future diagnostics applications. Most of the measured results, determined within an accuracy of 5%, are found to be in better agreement with HITRAN 2004 than with earlier editions of this database. Large discrepancies (>10%) between measurements and HITRAN 2004 database are identified for some of the probed transitions. These new spectroscopic data for H₂O provide a useful test of the sensor design capabilities of HITRAN 2004 for combustion and other applications at elevated temperatures.     

Criteria for selection of components for surrogates of natural gas and transportation fuels

The present paper addressed the production of soot precursors, acetylene, benzene and higher aromatics, by the paraffinic (n-, iso-, and cyclo-) and aromatic components in fuels. To this end, a normal heptane mechanism compiled from sub-models in the literature was extended to large normal-, iso-, and cyclo-paraffins by assigning generic rates to reactions involving paraffins, olefins, and alkyl radicals in the same reaction class. Lumping was used to develop other semi-detailed sub-models. The resulting mechanism for components of complex fuels (named the Utah Surrogate Mechanism) includes detailed sub-models of n-butane, n-hexane, n-heptane, n-decane, n-dodecane, n-tetradecane and n-hexadecane, and semi-detailed sub-models of i-butane, i-pentane, n-pentane, 2,4-dimethyl pentane, i-octane, 2,2,3,3-tetramethyl butane, cyclohexane, methyl cyclohexane, tetralin, 2-methyl 1-butene, 3-methyl 2-pentene and aromatics. Generic rates of reaction classes were found adequate to generate reaction mechanisms of large paraffinic components. The predicted maximum concentrations of the fuel, oxidizer, and inert species, major products and important combustion intermediates, which include critical radicals and soot precursors, were in good agreement with the experimental data of three premixed flames of composite fuels under various conditions. The relative importance in benzene formation of each component in the kerosene surrogate was found to follow the trend aromatics > cyclo-paraffins > iso-paraffins > normal-paraffins. In contrast, acetylene formation is not that sensitive to the fuel chemical structure. Therefore, in formulation of surrogate fuels, attention should be focused on selecting components that will yield benzene concentrations comparable to those produced by the fuel, with the assurance that the acetylene concentration will also be well approximated.     

Open-path ozone detection by quantum-cascade laser

Open-path ozone measurements performed by mid-IR differential absorption spectroscopy are reported. Ozone spectrum was taken by fast repetitive sweeping of a quantum-cascade laser wavelength over a spectral feature from the ν₃ absorption band of ozone, centered at 1031.2 cm^-1. Short (100 ns) sweeping times were essential to prevent line-distortions caused by atmospheric turbulence. For fast wavelength sweeping, a technique that employed the thermal chirp during 140 ns excitation pulses was used. The lowest detection limit of 0.3 ppm.m was estimated from the minimum detectable differential absorption. We present the results from cell and open-path measurements over 440 and 5800 m, together with experimental data regarding the tuning range, the tuning rate and the tuning linearity of the QCL while operated with 140 ns excitation pulses. PACS 42.62.Fi; 82.80.Gk; 92.60.Sz     

Measurement of UV absorption of single living cell for cell manipulation using NIR femtosecond laser

Optical UV absorption of single human living cells ranging from 200 nm to 360 nm was measured in situ for the study of cell manipulation using the near-infrared (NIR) femtosecond laser. Human breast living cells of MCF-10A, MCF-7, and MDA-MB-231 were used in this experiment. The selective photo-disruptions of single living cell and its sub-organelle (nucleus) were also demonstrated using the tightly focused 790 nm wavelength femtosecond laser with pulse duration of 110 fs. It was found that each living cell has its own absorption spectrum in UV wavelength ranges. It was also inferred that intrinsic absorption spectrum is attributed to the amount of DNA and protein of living cell. For the study of photo-disruption of single cell using the multi-photon absorption excited by the NIR femtosecond laser pulse, the origin UV absorption spectrum of targeted living cell is important and fundamental information to understand nonlinear interaction between NIR ultrashort, high-intensity laser light and transparent living cell.     

Low-temperature absorption edge and photoluminescence in layered structured Tl2Ga2S3Se single crystals

The absorption edge of undoped Tl₂Ga₂S₃Se crystals have been studied through transmission and reflection measurements in the wavelength range 440–1100 nm and in the temperature range 10–300 K. The absorption edge was observed to shift toward lower energy values with increasing temperature. As a result, the rate of the indirect band gap variation with temperature γ=−2.6×10⁻⁴ eV/K and the absolute zero value of the band gap energy E_gi(0)=2.42 eV were obtained.     

Autoignition of gasoline surrogate mixtures at intermediate temperatures and high pressures: Experimental and numerical approaches

Ignition-delay times were measured in shock-heated gases for a surrogate gasoline fuel comprised of ethanol/iso-octane/n-heptane/toluene at a composition of 40%/37.8%/10.2%/12% by liquid volume with a calculated octane number of 98.8. The experiments were carried out in stoichiometric mixtures in air behind reflected shock waves in a heated high-pressure shock tube. Initial reflected shock conditions were as follows: Temperatures of 690-1200 K, and pressures of 10, 30 and 50 bar, respectively. Ignition delay times were determined from CH^∗ chemiluminescence at 431.5 nm measured at a sidewall location. The experimental results are compared to simulated ignition delay times based on detailed chemical kinetic mechanisms. The main mechanism is based on the primary reference fuels (PRF) model, and sub-mechanisms were incorporated to account for the effect of ethanol and/or toluene. The simulations are also compared to experimental ignition-delay data from the literature for ethanol/iso-octane/n-heptane (20%/62%/18% by liquid volume) and iso-octane/n-heptane/toluene (69%/17%/14% by liquid volume) surrogate fuels. The relative behavior of the ignition delay times of the different surrogates was well predicted, but the simulations overestimate the ignition delay, mostly at low temperatures.