Erratum to: High speed mixture fraction and temperature imaging of pulsed, turbulent fuel jets auto igniting in high temperature, vitiated co flows

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DOI 10.1007/s00348-015-2101-9 ERRATUM Erratum to: High speed mixture fraction and temperature imaging of pulsed, turbulent fuel jets auto igniting in high temperature, vitiated co flows Michael J. Papageorge 1 Christoph Arndt 2 Frederik Fuest 1 Wolfgang Meier 2 Jeffrey A. Sutton 1 Published online: 28 December 2015 Springer-Verlag Berlin Heidelberg 2015 Erratum to: Exp Fluids (2014) 55:1763 DOI 10.1007/s00348 014 1763 z In the original publication the experimental approach to simultaneously measure quantitative time-resolved image sequences of mixture fraction and temperature during pulsed fuel injection into a high-temperature, vitiated, oxidizer stream is presented. The methodology and scalar results (mixture fraction and temperature) as presented are correct, but unfortunately the fuel tube diameter of 2 mm for the DLR jet-in-hot-co-flow (JHC) is incorrect, which leads to errors in the presentation of results in the original publication. The correct fuel tube diameter is 1.5 mm, which changes the reported operating conditions and normalized spatial locations of the measurements. Many measurement locations (axial and radial) reported were normalized by the tube diameter (d). While the normalized spatial positions are incorrect, the absolute spatial positions are correct. In this erratum, the correct operating conditions are presented along with corrected figures and figure captions using absolute spatial position to avoid confusion. When referring to the original publication, any reported normalized spatial position (x/d or r/d) in the text should be multiplied by 2 to yield the correct spatial position in units of millimeters. Presentation of results Table 1 in the original publication contains operating conditions for five experimental test cases. The operating conditions (accounting for the correct fuel tube diameter) should have been presented as shown below (Table 1). The presentation of Figs. 3b, 6, 10, 11, 13, 14, 15, 16, 17, 18, and 19 is incorrect in the original publication. The correct figure presentation and figure captions are presented here (Figs. 3b, 6, 10, 11, 13, 14, 15, 16, 17, 18, 19). The online version of the original article can be found under doi:10.1007/s00348-014-1763-z. * Jeffrey A. Sutton sutton.235@osu.edu 1 2 Department of Mechanical and Aerospace Engineering, Ohio State University, Columbus, OH, USA Institute of Combustion Technology, German Aerospace Center (DLR), Stuttgart, Germany

14 Page 2 of 6 Table 1 Operating conditions Jet Co-flow Fuel U (m/s) Re φ Ṁ (kg/s) T ox (K) T ad (K) a XN b 2 XO b 2 XH b 2 O CH 4 177 15,400 0.029 0.465 4.8 10 3 1490 1563 0.719 0.102 0.178 CH 4 177 15,400 0.028 0.485 4.7 10 3 1520 1603 0.716 0.097 0.185 CH 4 177 15,400 0.027 0.506 4.5 10 3 1540 1646 0.714 0.093 0.192 DME 144 44,510 0.064 0.380 5.6 10 3 1330 1372 0.731 0.120 0.148 C 3 H 8 129 39,590 0.040 0.360 5.8 10 3 1274 1326 0.730 0.128 0.141 a Calculated with a reactant temperature of 290 K b Determined during data processing as described in Sect. 3.2 (a) (b) From HEPBLS Mixture Fraction (ξ) Mixture Fraction (ξ) x= 40 mm x= 40 mm CH 4 C 3 H 8 T(K) T(K) Hot coflow air Mixture Fraction (ξ) x= 40 mm Residence Time (ms) DME T(K) Fig. 3 a Schematic of the high-speed imaging setup used for the auto-ignition experiments. b Photograph of a Re = 44,510 DME flame (1330 K oxidizer) under steady operating conditions X fuel /X fuel,o Fig. 6 Results from a series of plug flow reactor (PFR) simulations showing the normalized fuel mole fraction (X fuel /X fuel,o ) as a function of mixture fraction/temperature and PFR residence time (τ R ). A value of X fuel /X fuel,o = 1 indicates that no reaction of the fuel has taken place at a given time, τ R. The white solid contour is an estimated maximum residence time for the cold jet-in-hot-co-flow conditions at an axial position of x = 40 mm. The white dotted line represents the stoichiometric mixture fraction,, value

Page 3 of 6 14 T (K) T (K) 1600 1500 1400 1400 1300 1200 T ad T ad φ = 0.466 φ = 0.38 ξ /ξ cl 1.2 1.0 0.8 0.6 0.4 0.2 Cold Jet (Re = 10,000) Cold Jet ( Re = 30,000) CH4 (Tox = 1490K) C3H8 (Tox = 1280K) DME (Tox = 1320K) T (K) 1350 1250 φ = 0.36 1150-20 -10 0 10 20 T ad Radial Position (mm) Fig. 10 Radial profiles of the oxidizer temperature (no jet flow) at an axial position of 40 mm downstream of the fuel tube exit for three experimental cases shown in Table 1. The red line represents an instantaneous profile, and the black line represents the average from 100 profiles. The dashed line represents the adiabatic flame temperature, T ad, and is shown for reference 0.0 0 0.5 1 1.5 2 2.5 r/r 1/2 Fig. 13 Normalized mixture fraction (ξ/ξ cl ) profiles as a function of normalized radial position (r/r 1/2 ). The dashed lines correspond to T = 300 K, non-reacting propane jets issuing into air measured 160 mm downstream of an 8-mm tube. The solid lines correspond to the fuel jets in hot, vitiated co-flows as identified in Table 1, measured 40 mm downstream of the exit of the current 1.5-mm tube. Note all curves exhibit self-similarity and collapse upon one another 0.1 φ = 0.36 φ = 0.38 σ = 11.7 K σ = 13.2 K pdf (-) 0.01 φ = 0.466 σ = 25.8 K 0.001 1200 1300 1400 1500 1600 Temperature (K) Fig. 11 Probability density functions (pdf) of the measured oxidizer temperature for three experimental cases shown in Table 1. The pdf was constructed from a single, instantaneous image representing 15,000 data points from radial positions spanning 12 18 mm from centerline at axial locations spanning 34 46 mm downstream of the fuel tube exit. The standard deviation derived from each pdf is listed above the corresponding distribution

14 Page 4 of 6 Fig. 14 Example 10-kHz image sequence of the transient fuel injection of C 3 H 8 into a T = 1270 K co-flow at an axial position of 40 mm downstream of the fuel tube exit. The steadystate Reynolds number of the jet is 39,590 Fig. 15 Example image sequences of the 10-kHz OH* CL fields. The top rows of each sequence correspond to the OH* emission as viewed from OH* CL Camera 1 in Fig. 3a, and the bottom rows correspond to the OH* emission as viewed from OH* CL Camera 2 in Fig. 3a. a Initial kernel forms within the laser sheet used for planar Rayleigh scattering. b Initial kernel forms outside of the laser sheet

Page 5 of 6 14 Fig. 16 Example 10-kHz image sequences of mixture fraction (top), OH* CL (middle), and temperature (bottom) for the case of C3H8 auto-igniting in a T = 1270 K co-flow. The circled regions correspond to the spatial location of the initial ignition kernel formation and subsequent displacement Fig. 17 Example 10-kHz image sequences of mixture fraction (top), OH* CL (middle), and temperature (bottom) for the case of CH4 auto-igniting in a T = 1490 K co-flow. The circled regions correspond to the spatial location of the initial ignition kernel formation and subsequent displacement 13

14 Page 6 of 6 Fig. 18 Example ten-frame, 10-kHz image sequence of OH* CL (top) and temperature (bottom) for the case of DME auto-igniting in a T = 1330 K co-flow. The circled regions correspond to the spatial location of the initial ignition kernel formation and subsequent displacement 48 x (mm) 40 32-8 0 8 r (mm) Fig. 19 Example image sequence of the logarithm of the scalar dissipation rate for the case of DME auto-igniting in a T = 1330 K coflow. The five images correspond to frames 2 6 of Fig. 18. Overlaid on the scalar dissipation rate layers are the stoichiometric mixture fraction contour (, shown as blue solid line) and a T = 1380 K isocontour (red line) denoting the onset and initial displacement of the auto-ignition kernel