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NASA Technical Reports Server (NTRS) 20000091021: Raman Gas Species Measurements in Hydrocarbon-Fueled Rocket Engine Injector Flows PDF

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Preview NASA Technical Reports Server (NTRS) 20000091021: Raman Gas Species Measurements in Hydrocarbon-Fueled Rocket Engine Injector Flows

AIAA 2000-3391 Raman Gas Species Measurements in Hydrocarbon- Fueled Rocket Engine Injector Flows J. Wehrmeyer Mechanical Engineering Department Vanderbilt University Nashville, TN 37235 R. Hartfield Aerospace Engineering Department Auburn University Auburn, AL 36849 H. Trinh, C. Dobson, and R. Eskridge Space Transportation Directorate NASA-Marshall Space Flight Center Huntsville, AL 35812 36 th AIAA/ASME/SAE/ASEE Joint Propulsion Conference & Exhibit 17-19 July 2000 Huntsville, Alabama Raman Gas Species Measurements in Hydrocarbon-Fueled Rocket Engine Injector Flows Joseph A. Wehrmeyer* Mechanical Engineering Department, Vanderbilt University, Nashville, TN 37235 Roy J. Hartfield, Jr] Aerospace Engineering Department, Auburn University, Auburn, AL 36849 Huu P. Trinh, _Chris C. Dobson, _and Richard H. Eskridge _ Space Transportation Directorate, NASA-Marshall Space Flight Center, Huntsville, AL 35812 Abstract Hardware associated with this effort includes Rocket engine propellent injector an optically-accessible high pressure combustion development at NASA-Marshall includes experimental chamber sized for single-element fuel injectors analysis using optical techniques, such as Raman, (Unielement Test Articlel and a newer, larger Modular fluorescence, or Mie scattering. For the application of Combustion Test Article (MCTA_ that can spontaneous Raman scattering to hydrocarbon-fueled accommodate multi-element fuel injector flows a technique needs to be developed to remove the configurations and that is also optically-accessible. intert'ering polycyclic aromatic hydrocarbon Optical accessibility allows laser-based methods, such fluorescence from the relatively weak Raman signals. as laser Mie scattering, fluorescence, and spontaneous A current application of such a technique is to the Raman scattering, to be applied. Raman spectroscopy analysis of the mixing and combustion performance of has been used to analyze an oxygen-rich gaseous multijet, impinging-jet candidate fuel injectors lbr the hydrogen/liquid oxygen (GH2/LOx) injector flow in the baseline Mars ascent engine, which will burn methane unielement test article (1) and most recently is being and liquid oxygen produced in-situ on Mars to reduce considered lbr use in the MCTA to analyze the mixing the propellent mass transported to Mars for future and combustion performance of multijet, impinging-jet manned Mars missions. The Raman technique takes candidate fuel injectors for the baseline Mars ascent advantage of the strongly polarized nature of Raman engine (2). This engine will burn methane (CH4) and scattering. It is shown to be discernable from LOx produced in-situ on Mars to reduce the propellent unpolarized fluorescence interference by subtracting mass transported to Mars for future manned Mars one polarized image from another. Both of these missions (3). polarized images are obtained from a single laser pulse by using a polarization-separating calcite rhomb Application of Raman spectroscopy to mounted in the imaging spectrograph. A hydrocarbon-fueled combustion brings the issue of demonstration in a propane-air flame is presented, as interference of the weak Raman scattering light signals well as a high pressure demonstration in the NASA- with strong laser-induced fluorescence. The Marshall Modular Combustion Test Artice, using the fluorescence interference can be from polycyclic liquid methane-liquid oxygen propellant system. aromatic hydrocarbons (PAH's) which are excited and fluoresce across the ultraviolet and visible spectrum (4) Introduction and when using ultraviolet lasers can be due to the Technology development associated with hydroxyl radical (OH) and to vibrationally-excited 02, advanced space transportation propulsion systems both of which are present in combustion reaction zones includes design and analysis of new types of propellent (5). By taking advantage of the polarization properties injectors. An effort exists at NASA-Marshall to of Raman scattering, it is possible to discriminate the include experimentally-obtained reactant/product Raman signal from interfering fluorescence mixing/combustion intbrmation as part of the injector interference and hence apply Raman scattering to the analysis. analysis of hydrocarbon-fueled combustion. This can be done by obtaining two Raman images, one using a *Research Associate Prof., Senior Member, AIAA vertically polarized laser and one using a horizontally- Associate Prof., Senior Member, AIAA polarized laser, and then subtracting the intensity of - Engineer. Senior Member. AIAA one image from another to obtain a net Raman signal Physicist, Propulsion Research Center (6). A second method that lends itself to single-pulse IEngineer. Propulsion Research Center (and hence instantaneous_ measurements is to obtain Cop)right © 2000 by J. A. Wehrmeyer. Published by two simultaneous Raman images created from the same the American Institute of Aeronautics and laser pulse. One of these images is the vertically- Astronautics, Inc. with permission. polarized signal and one is for the horizontally- polarized signal. The difference between these images providesthenetRamansignal,freeof fluorescence fluorescence-free UV Raman measurements have been interferenceT.histechniquheasbeendemonstratfeodr obtained in an iso-octane fueled engine -'_by placing a a time-averageadpplication(7) andthis paper Glan prism at the focal plane of the imaging describeassingle-pulsaepplicatioonfthetechnique. spectrograph, and then refocusing the two polarized spectra onto two separate ICCD cameras. Another Single-Pulse Polarized UV Raman Measurements method uses a calcite rhomb located at the While visible lasers may be best at providing spectrograph entrance slit to displace the horizontally- interference-free Raman data for steady, laminar polarized light from the vertically polarized light and has been used to obtain time-averaged PAH flames, it may still be desirable to use a UV laser, when fluorescence-free UV Raman spectra in C3Hs-fueled probing turbulent flames, in order to obtain sufficient flames. 2s This latter method is described here, and signal strength for single-pulse measurements. By single-pulse UV Raman images in a C_Hs-air flame are exploiting the differences in polarization properties presented. bet_een Raman and PAH fluorescence, it is possible :o Figure 14 sho,xs the UV Raman system used obtain UV Raman signals in PAH-ridden for polarization-resolved measurements. It represents a environments. typical UV Raman system except /'or one unique In addition to laser wavelength, the signal feature: a calcite rhomb inserted just behind the strength of Raman scattering depends on two molecular entrance slit of the spectrograph. This optical element invariants, the square of the mean polarizability (a')-" displaces the horizontally polarized Raman image and the square of the anisotropic polarizability ('/'V. about 5 mm from the vertically polarized Raman These are used to determine a constant _, which can be image, which travels directly straight through the considered as the Raman scattering cross section for a rhomb. The length of the entrance slit is limited to 4 single molecule, not including the laser wavelength mm to keep the two polarized images from contribution. The value of qb also depends on the overlapping. Figure 15 shows a typical single-pulse polarization of the incident laser beam, the polarization image obtained from the experimental system, and this of the detected Raman signal, and the angle of detected image shows the relative strength of vertically Raman signal with respect to incoming laser beam. polarized signal compared to horizontally polarized For a 90°collection angle and for the Raman and laser signal. The H20 Raman signal (from air humidity) is beams both in a horizontal plane, the value of ¢_ for almost completely polarized, while the N, signal is vertically polarized Raman scattering is:22 slightly depolarized and the O, signal is more depolarized than N,. This corresponds to others" O0= (a'}'- + 1/45 (7'_: experimental or._servat-m-ns. 8.26 Spatially-integrated single-pulse Raman and for horizontally polarized Raman scattering ¢_is: spectra are shown in Fig. 16, obtained from a slightly premixed C3Hs-air bunsen flame. One of these spectra (b = t/60 (7')2 is the vertically polarized Raman-fluorescence signal. The horizontally polarized signal shows essentially Usually a'-" and y': are similar in magnitude only the fluorescence signal, that has two contributions. and the vertically polarized light is almost two orders A broadband component is caused by PAH of magnitude greater than the horizontally polarized fluorescence, extending from below 255 nm to above light. Thus the Raman scattering signal essentially 275 nm. A second contribution to the fluorescence retains the polarization of the incoming laser beam. background is the OH fluorescence from about 265 to Ho_e',er a fluorescence light emission process does 270 nm. caused by tuning the laser slightly onto a not retain the laser polarization because of the strong OH transition. This is done to demonstrate the relatively long time the molecule exists in the excited ability of the technique to simultaneously measure state before fluorescing. During this time the molecule Raman spectra and OH fluorescence. Before rotates, eliminating any correlation between the subtracting the horizontally polarized signal from the polarization of absorbed and emitted photons. vertical it is first multiplied by a factor of 2.22 to By providing two laser pulses, one account for the ratio in transmission efficiency (for the horizontally polarized and the other vertically spectrometer/calcite rhomb) between the vertically and polarized, two signal spectra can be obtained, with one horizontally polarized signals. The net signal shows a containing both Raman and fluorescence and one fluorescence-flee Raman spectrum that reveals the containing essentially only fluorescence. This method simultaneous occurrence of CO2 and H_,O (products of has been used to obtain fluorescence-tree, time- combustion). CO and H: (intermediate products), and averaged UV Raman measurements in hydrocarbon unburned C_Hs. Information about the spatial structure flames, s-'3 Single-pulse, polarization-resolved. of the flame can be revealed in the single-pulse image ofFig.17.ThisimagsehowusnburneCd3Ho8ccurring operational sequence is to introduce CI-I4 without 02. nearthe0mmposition.Thecoolerd,enseurnburned This shows as a strong CH4 Raman signal occurring in gasmixturealsoprovideasstrongeNr_R, amasnignal the image for 1.8 sec. Alter injection of CI-L comes nearthatlocationA. t~1.5mmtheC3Hp8yrolizeisnto injection of 02 to commence main stage combustion. otherhydrocarboninsc,ludingPAH'sthatcausaestrip The images obtained during this part of the sequence ofbroadbanfdluorescentcoeappeaartthislocation. are all similar to the lower right one in Fig. 2 in that Fartherintotheflamechemicarleactionisnvolving there is significant broadband emission occurring oxidationtakeplace,creatingtheOHintermediate. across most of the spectrum, and the Raman signals for ThisshowsupinFig.17bythereplacemeonftPAH the reactants and products have all diminished because fluorescenwceithOHfluorescenacteflamepositions of the increased temperature and reduced density greatetrhan-2.5mm.Bysubtractinthgescaleudpper during main stage combustion. partof Fig.17(horizontallpyolarizedfluorescence signal)fromthebottompart(verticallypolarized The question as to whether the broadband signal)a,ndb?summintghenetRamasnignafloreach emission is caused by laser-induced fluorescence, by location(wavelengitnhtegrationa)qualitativpeicture direct flame emission, or by a combination was ofthestructuroeftheflamecanbediscerneads,inFig. answered by the results of one of the other tests, the 18.ThisfigureshowtshedropinC3Hssignaalndthe one wich did not have a laser beam entering the concurrenitncreasein H20signal,showingthe combustion chamber. The images obtained during that formationofthatproducotccurringclosetothefuel test had about one half of the emission intensity as zone.Inthesameregionthe H2 and CO signals are from Test 25, indicating that constant flame emission generally higher than in the fuel zone or in the OH contributes about half of the interference background. reaction zone past 2.5 ram. The exposure time used for the camera was 200 nsec and could be reduced down to 20 nsec, the time span of Hot-fire tests from Modular Combustion Test the laser pulse. Doing so would reduce the detected Article (MCTA) burning liquid CH4&.__&_O, flame luminosity by a factor of ten. The polarization-resolved UV Raman spectroscopy system has been applied to the analysis of Other parts of the hot fire test sequence are liquid-CH4/LOx combustion in the modular shown in the remaining images of Fig. 3. These are for combustion test article (MCTA) at Test Stand 115 of the following events: LOx valve closing, LOx valve NASA-Marshall.. completely off, and both propellents off with only the N2 purge remaining at the end of the test. Three hot fire tests were performed that involved use of the Raman system. Of these three, The utility of the polarization resolved only one provided Raman data in conjunction with a imaging becomes important when trying to detect hot fire test. One test resulted in an early cut and thus Raman signals among the unpolarized interference never provided main stage operation. One test was a background. However when the vertical polarized successful run of the MCTA, but the Raman system imaged is scaled (to account for transmission efficiency laser beam did not enter the test article during the test differences in the spectrogaph and calcite crystal) and because a mirror directing the beam into the test article subtracted from the horizontally polarized imaged, no was wrongly oriented. However the images obtained net Raman signal is left for the main stage images, one during this test did provide some useful intbrmation, as of which is shown in Fig. 4. The problem occurs mentioned below. because there is approximately the same amount of Raman signal occurring in the vertically polarized Figures 2 and 3 show selected Raman images image as for the horizontally polarized image, for both from the successful test. These images are taken from N,_ and for CHa, and probably ['or the other species" a group of I(X), which were obtained at 5 Hz over a Raman signals. This is completely unexpected, since total time of 20 sec. The Raman images were initiated the Raman images of Ref. 1, and Raman theory, both at the beginning of the test, however the Raman images show that significantly less Raman signal should exist can be correlated to the known events occurring during at one polarization compared to the other. the test sequence. The first Raman image at time 0 sec {an arbitrary ret'erence timel shows the N_,purge as the The absence of a net Raman signal for the only gas present just before ignition. The next image main stage Raman images is a result of at least two in Fig. 2, at 0._ see.. shoves combustion of H_,and O,_ problems that must be surmounted. The first one occurring as the igniter becomes operational. This is involves the presence of Raman signals in both shown by the presence of their Raman signals in polarization images. This problem must be solved addition to the purge Raman signal. Next in the because the fundamental way that Raman signals are extractedfrominterferingbackgrounids by their Thermal and Fluids Analysis Workshop, highl?polarizecdharacteristicTsh.eseconpdroblem sponsored by NASA-Marshall Space Flight isthattheRamansignalsareweakcomparetdothe Center, Huntsville, AL, Sept. 13-17. back_oundR. amasnignasltrengtmhustbeimproved 3. Nandula, S. P., Brown, T. M., Pitz, R. W., and relativetobackgrounindterferencdeuringahotfire DeBarber, P. A., "Single-Pulse, Simultaneous test.Onewaytodothisistoreducteheexposurtieme Multipoint Multispecies Raman Measurements in ofthecamerdaowntothelaseprulselengthw,hichhas Turbulent Nonpremixed Jet Flames," Optics alreadybeenmentionedA. lsothesetestswereall Letters, Vol. 19, No. 6, 1994, pp. 414-416. performewdithanunfocuseladsebreamw, hichhasa 4. Reckers, W., Hiiwel, L., GrtineMd, G., and crosssectionof I cmby2 cm. Thebeamwasleft Andresen, P., "'Spatially Resolved Multispecies unfocusetodeliminatethepossibilitoyflasedramage and Temperature Analysis in Hydrogen Flames," totheMCTAopticawl indowsw,hichwasaproblem Applied Optics, Vol. 32, No. 6, 1993, pp. 907-918. whentheRamasnystemwasapplietdotheUnielement 5. Chen, Y.-C., and Mansour, M. S., "'Measurements TestArticle(Ref.1t. Bylightlyfocusindgownto,say acrosssectionof2 mmx 1mm,theRamansignal of the Detailed Flame Structure in Turbulent H,_- Air Jet Diffusion Flames with Line- strengtwhillbeimproverdelativetothebackgrounbdy asignificanatmounat,tleasat factoorftenbecausthee Raman/Rayleigh/LIPF-OH Technique," Twenty- Ramansignalwill occurovera narrowbandof Sixth Symposium (International) on Combustion, wavelengthinssteadof a broadwavelengtrhegion. Combustion Inst., Pittsburgh, PA, 1996, pp. 97- TheRamadnetectiosnystemcanalsobeplacedcloser 103. to theMCTAopticalwindowto increaseit light 6. Tacke, M. M., Cheng, T. C., Hassel, E. P., and gatherinpgower.Thisshouldresulitnabouatfactoorf Janicka. J., "'Study of Swirling Recirculating four increase in signal since it was approximately 20 Hydrogen Diffusion Flame Using UV Raman inches away and the lens system is designed for a Spectroscopy," Twent3.,-Sixth Symposium minimum distance of 10 inches between the sample (International) on Combustion, Combustion Inst.. volume and the first light collection lens. Pittsburgh, PA, 1996, pp. 169-175. 7. Frank, J. H., Lyons, K. M., Marran, D. F., Long, Conclusions and Future Work M. B., Stgrner, S. H., and Bilger, R. W., "Mixture The critical issue still unresolved, after the Fraction Imaging in Turbulent Nonpremixed first application of polarization-resolved UV Raman to Hydrocarbon Flames," Twenty-Fifth Symposium high pressure combustion, is the polarization of the (International) on Combustion, Combustion Inst., Raman signal. Do the polarization characteristics of Pittsburgh, PA, 1995, pp. 1159-1164. Raman scattering change as pressure is increased'? In 8. Schefer, R. W., Namazian, M., and Kelley, J., order to determine the effects of pressure on Raman •"CH, OH, and CH4 Concentration Measurements scattering polarization, a high pressure sample cell is in a Lifted Turbulent-Jet Flame," Twent3"-Third being constructed that can be used to both determine Symposium (International) on Combustion, the influence of gas pressure and glass properties upon Combustion Inst., Pittsburgh, PA, 1990, pp. 669- detected Raman signal polarization. 676. 9. Yeralan, S., Pal, S., and Santoro, R. J., "Major Acknowled2ments Species and Temperature Profiles of LOx/GH: This research is funded by NASA-Marshall Combustion," AIAA paper 97-2940, 1997. through a 1999 Summer Faculty Research Fellowship 10. Grtinefeld, G.. Beuhausen, V., and Andresen, P., and through Contract # H35139D. "'Interference-Free UV-Laser-Induced Raman and References Rayleigh Measurements in Hydrocarbon Combustion Using Polarization Properties," I. Wehrmeyer, J. A.. J. M. Cramer. R. H. Eskridge, C. C. Dobson. 1997. UV Raman Diagnostics for Applied Physics B, Vol. 61, 1995, pp. 473-478. Rocket Engine Injector Development. AIAA II. Masri, A. R., Bilger, R. W., and Dibble, R. W., Paper 97-2843 presented at the AIAA 33rd Joint "'Fluorescence" Interference with Raman Propulsion Conference, Seattle, WA, July 6-9 Measurements in Nonpremixed Flames of Methane," Combustion and Flame, Vol. 68, 1987, V_ehrmeyer, J. A., and H. P, Trinh. 1999. Raman pp. 109-119. Spectroscopy fi)r Instantaneous Multipoint. 12. Rabenstein, F., and Leipertz, A., "'One- Multispecies Gas Concentration and Temperature Dimensional, Time-Resolved Raman Measurements in Rocket Engine Propellent Measurements in a Sooting Flame Made with 355- Injector Flows. Paper presented at the 10a' nmExcitation," Applied Optics, Vol. 37, No. 21, Volume Fraction," Applied Physics B, Vol. 59, 1998, pp. 4937-4943. 1994, pp. 1994. 13. Takagi, Y., "'A New Era in Spark-Ignition Engines 21. Will, S., Schraml, S.. and Leipertz, A., "Two- Featuring High-Pressure Direct Injection," Dimensional Soot-Particle Sizing by Time- Twenty-Seventh Symposium (International) on Resolved Laser Induced Incandescence." Optics Combustion, Combustion Inst., Pittsburgh, PA, Letters, Vol. 20, 1995, pp. 2342-2344. 1998, pp. 2055-2068. 22. Wehrmeyer, J. A., Yeralan, S., and Tecu, K. S., 14. Kee, R. J., Rupley, F. M., Miller, J. A., Coltrin, M. "'Multispecies Raman Imaging in Flames by Use E., Grcar, J. F., Meeks. E., Moffat, H. K., Lutz, A. of an Unintensified Charge-Couple Device," E., Dixon-Lewis, G., Smooke, M. D., Warnatz, J., Optics Letters, Vol. 20. No. 8, 1995, pp. 934-936. Evans, G. H., Larson, R. S., Mitchell, R. E., 23. Miles, P. 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W., "'The Sensitive Systems: Spray Flame and Four-Cylinder In-Line Structure of Partially Premixed Methane-Air vs. Engine," Applied Physics B, Vol. 58, No. 4, 1994, Air Counterflow Flames," Twenty-Sixth pp. 333-342. Symposium (International) on Combustion, 26. Knapp, M., Luczak, A.. Beuhausen, V., Hentschel, Combustion Inst., Pittsburgh, PA, 1996, pp. 1121- W., Manz, P., and Andresen, P., "'Polarization 1128. Separated Spatially Resolved Single Laser Shot 17. Petarca, L., and Marconi, F., "Fluorescence Multispecies Analysis in the Combustion Chamber Spectra and Polycyclic Aromatic Species in a N- of a Realistic SI Engine with a Tunable KrF Heptane Diffusion Flame," Combustion and Excimer Laser." Twenty-Sixth Symposium Flame Vol. 78. 1989. pp. 308-325. (International) on Combustion, Combustion Inst., 18. Beretta, F.. Cincotti. V., D'Alessio. A., and Pittsburgh, PA, 1996. pp. 2589-2596. Menna. P.. "'Ultraviolet and Visible Fluorescence 27. Hartfield, R., Dobson. C., Eskridge. R., and in the Fuel Pyrolysis Regions of Gaseous Wehrmeyer. J., "'Development of a Technique for Diffusion Flames," Combustion and Flame Vol. Separating Raman Scattering Signals from 61, 1985, pp. 211-218. Back_ound Emission with Single-Shot 19. Miller, J. H., Mallard, W. G., and Smyth, K. C., Measurement Potential," AIAA Paper 97-3357, "'The Observation of Laser-Induced Visible 1997. Fluorescence in Sooting Diffusion Flames," 28. Penney, C. M., Goldman, L. M., and Lapp, M., Combustion and Flame Vo[. 47, 1982, pp. 205- "'Raman Scattering Cross Sections." Nature 214. PhvsicalScience, Vol. 235. 1971, pp. I10-112. 20. Vander Wal, R. L., and Weiland, K. J., "'Laser- Induced Incandescence: Development and Characterization Towards a Measurement of Soot- o_G_"rA_-CAME'RA W_.TH / GATED IHTEN'_F_ER mFOC&L LENGTH LENS puLSE9 U_ C_.LCITE RHOMB _l.v_ I_'T_ j J" j1_. z./ ,,=, N a,. --I < I--N o 255 WAVELENGTH, nm 277 -ifN_l@ o t 2 3 _mm 704e * l _P&IVlBJEkIOT_ nm

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