• Energy Research

Abstract Species concentration (e.g. CO) and temperature measurements in the combustion field require fast-response technique without interfering species. In the last decade, tunable diode lasers have been established as strong technique to measure species such as CO, CO2, and H2O as well as temperature with high sensitivity. The drawback is the degree of interference that might hamper the robustness of the technique. In this work simultaneous measurements of temperature and CO concentration were carried out using an interference-free mid-infrared laser-based absorption technique behind reflected shock waves. Two transition lines of CO (P(v″ = 0, J″ = 21) and P(v″ = 1, J″ = 21)) in the fundamental vibrational band near 4.87 and 4.93 μm, respectively, were selected. Absorbance interferences from CO2 and H2O at room and high temperatures were evaluated. Spectroscopic parameters for the development of the system were measured: line strengths and collisional broadening coefficients (in Ar) of both lines were obtained at 1020–1950 K by using the scanned-wavelength direct-absorption method. The technique was demonstrated for non-reactive and reactive mixtures. For the non-reactive case, temperature and CO concentration were measured at 1030–1910 K and 1.0–3.7 bar. For the reactive case, oxidation of i-C8H18/O2/Ar and i-C8H18/C2H5OH/O2/Ar mixtures were investigated at three equivalence ratios of 2.0, 1.0, and 0.5. The two newly adopted lines exhibited good performance in the detection of CO concentration and are immune to interferences from CO2 and H2O. In addition, the simulated data from the state-of-the-art isooctane/ethanol mechanisms in literature were compared with the measured data, showing overall good agreement.

Abstract Species concentration (e.g. CO) and temperature measurements in the combustion field require fast-response technique without interfering species. In the last decade, tunable diode lasers have been established as strong technique to measure species such as CO, CO2, and H2O as well as temperature with high sensitivity. The drawback is the degree of interference that might hamper the robustness of the technique. In this work simultaneous measurements of temperature and CO concentration were carried out using an interference-free mid-infrared laser-based absorption technique behind reflected shock waves. Two transition lines of CO (P(v″ = 0, J″ = 21) and P(v″ = 1, J″ = 21)) in the fundamental vibrational band near 4.87 and 4.93 μm, respectively, were selected. Absorbance interferences from CO2 and H2O at room and high temperatures were evaluated. Spectroscopic parameters for the development of the system were measured: line strengths and collisional broadening coefficients (in Ar) of both lines were obtained at 1020–1950 K by using the scanned-wavelength direct-absorption method. The technique was demonstrated for non-reactive and reactive mixtures. For the non-reactive case, temperature and CO concentration were measured at 1030–1910 K and 1.0–3.7 bar. For the reactive case, oxidation of i-C8H18/O2/Ar and i-C8H18/C2H5OH/O2/Ar mixtures were investigated at three equivalence ratios of 2.0, 1.0, and 0.5. The two newly adopted lines exhibited good performance in the detection of CO concentration and are immune to interferences from CO2 and H2O. In addition, the simulated data from the state-of-the-art isooctane/ethanol mechanisms in literature were compared with the measured data, showing overall good agreement.

Abstract This paper used the opposed-flow flame model and GRI 3.0 mechanism to investigate NO emission characteristics of H2-rich and H2-lean syngas under diffusion and premixed conditions, respectively, and analyzed influences of adding H2O, CO2 and N2 on NO formation from the standpoint of thermodynamics and reaction kinetics. For diffusion flames, thermal route is the dominant pathway to produce NO, and adding N2, H2O and CO2 shows a decreasing manner in lowering NO emission. The phenomenon above is more obvious for H2-rich syngas because it has higher flame temperature. For premixed flames, adding CO2 causes higher NO concentration than adding H2O, because adding CO2 produces more O radical, which promotes formation of NO through NNH + O = NH + NO, NH + O = NO + H and reversed N + NO = N2 + O. And in burnout gas, thermal route is the dominant way for NO formation. Under this paper's conditions, adding N2 increases the formation source of NO as well as decreases the flame temperature, and it reduces the NO formation as a whole. In addition, for H2-lean syngas and H2-rich syngas with CO2 as the diluent, N + CO2 = NO + CO plays as an important role in thermal route of NO formation.

Abstract This paper used the opposed-flow flame model and GRI 3.0 mechanism to investigate NO emission characteristics of H2-rich and H2-lean syngas under diffusion and premixed conditions, respectively, and analyzed influences of adding H2O, CO2 and N2 on NO formation from the standpoint of thermodynamics and reaction kinetics. For diffusion flames, thermal route is the dominant pathway to produce NO, and adding N2, H2O and CO2 shows a decreasing manner in lowering NO emission. The phenomenon above is more obvious for H2-rich syngas because it has higher flame temperature. For premixed flames, adding CO2 causes higher NO concentration than adding H2O, because adding CO2 produces more O radical, which promotes formation of NO through NNH + O = NH + NO, NH + O = NO + H and reversed N + NO = N2 + O. And in burnout gas, thermal route is the dominant way for NO formation. Under this paper's conditions, adding N2 increases the formation source of NO as well as decreases the flame temperature, and it reduces the NO formation as a whole. In addition, for H2-lean syngas and H2-rich syngas with CO2 as the diluent, N + CO2 = NO + CO plays as an important role in thermal route of NO formation.

Abstract The oxidation of CH4/diethyl ether mixtures was studied with laser absorption-based time-resolved temperature and CO concentration measurements behind reflected shock waves. Fuel-rich (equivalence ratio ϕ = 2.0) mixtures were studied because of their relevance for mechanism development for partial oxidation reactions in the context of polygeneration processes and measurements at ϕ = 0.5 and 1.0 were used to verify the mechanism performance in an extended range of equivalence ratios. Temperature and CO concentration were measured via absorption using two fundamental vibrations of CO (ν" = 0, P20 and ν" = 1, R21) with two mid-IR quantum-cascade lasers near 4.8546 and 4.5631 µm. Interference from broadband absorption of CO2 in the region near 4.56 µm was quantified based on measured temperature-dependent CO2 absorption cross-sections and mechanism-based prediction of CO2 concentrations. The measured temporal CO-concentration and temperature profiles were compared with simulations based on two mechanisms (Fikri et al., 2017; Yasunaga et al., 2010). For mixtures with ϕ = 0.5, the two mechanisms show similar results, and well reproduce the experimental data. At ϕ = 1.0 and 2.0, the Fikri et al. mechanism shows very good agreement with the experiments whereas the Yasunaga et al. mechanism predicts a too fast CO-concentration and temperature rise.

Abstract The oxidation of CH4/diethyl ether mixtures was studied with laser absorption-based time-resolved temperature and CO concentration measurements behind reflected shock waves. Fuel-rich (equivalence ratio ϕ = 2.0) mixtures were studied because of their relevance for mechanism development for partial oxidation reactions in the context of polygeneration processes and measurements at ϕ = 0.5 and 1.0 were used to verify the mechanism performance in an extended range of equivalence ratios. Temperature and CO concentration were measured via absorption using two fundamental vibrations of CO (ν" = 0, P20 and ν" = 1, R21) with two mid-IR quantum-cascade lasers near 4.8546 and 4.5631 µm. Interference from broadband absorption of CO2 in the region near 4.56 µm was quantified based on measured temperature-dependent CO2 absorption cross-sections and mechanism-based prediction of CO2 concentrations. The measured temporal CO-concentration and temperature profiles were compared with simulations based on two mechanisms (Fikri et al., 2017; Yasunaga et al., 2010). For mixtures with ϕ = 0.5, the two mechanisms show similar results, and well reproduce the experimental data. At ϕ = 1.0 and 2.0, the Fikri et al. mechanism shows very good agreement with the experiments whereas the Yasunaga et al. mechanism predicts a too fast CO-concentration and temperature rise.