Article

Superlinear Enhancement of Discharge Driven Electric Oxygen-Iodine Laser by Increasing g0Lg_{0}{L}

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Abstract

Continuing experiments with electric oxygen-iodine laser (ElectricOIL) technology have significantly increased laser power output by increasing the product of gain and gain-length, g0Lg_{0}L. The authors report on progress with recent ElectricOIL devices utilizing a new concentric discharge geometry with improved O2(a1Δ){\rm O}_{2}(a^{1}\Delta) production at higher discharge operating pressure at higher system flow rates. O2(a1Δ){\rm O}_{2}(a^{1}\Delta) produced in flowing radio-frequency discharge in O2-He-NO{\rm O}_{2}\hbox{-}{\rm He}\hbox{-}{\rm NO} gas mixture is used to pump I(2P1/2)I(^{2}P_{1/2}) by near-resonant energy transfer, and laser power is extracted on the I(2P1/2)I(2P3/2)I(^{2}P_{1/2})\rightarrow I(^{2}P_{3/2}) transition at 1315 nm. Advancements in heat exchanger design reduce O2(a1Δ){\rm O}_{2}(a^{1}\Delta) wall loss without sacrificing significant cooling efficiency improving best gain performance from 0.26 to 0.30% cm1{\rm cm}^{-1}. Modeling of recent data is presented. By increasing the gain length (system size) by a factor of 3, a 5-fold increase in laser output on the 1315-nm transition of atomic iodine was achieved. Flow conditions with g0L=0.042g_{0}L=0.042 were used to extract a continuous wave average total laser power of 481 W. A low frequency ±11.9%{\pm}{11.9\%} oscillation in the total power was observed giving a peak outcoupled power of 538 W.

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... Since the first reporting of a viable electric discharge driven oxygen-iodine laser system (also often referred to as ElectricOIL or DOIL in the literature), there have been a number of other successful demonstrations of gain and laser power; Ionin [Ionin, 2007] and Heaven [Heaven, 2010a] provide comprehensive topical reviews of discharge production of O2(a) and various EOIL studies. The highest EOIL output power reported to date is > 500 W and the technology shows superlinear scaling with g0L [Benavides, 2012]. Computational modeling of the discharge and post-discharge kinetics [Stafford, 2004;Palla, 2006;Palla, 2007;Palla, 2010] has been an invaluable tool in EOIL development, allowing analysis of the production and depletion of various discharge species [such as O2(a), O2(b 1 ), O-atoms, and O3] and determination of the influence of NOX species on system kinetics. ...
... During the evolution of the EOIL technology development it became clear that it was critical to create post-discharge heat exchangers (HXs) that would significantly cool the gas flow while simultaneously (i) minimizing any loss of the critical O2(a), (ii) significantly reducing the detrimental O-atoms, and (iii) minimizing pressure drop for downstream pressure recovery reasons. This led to a series of BLAZE studies in which different geometries of cross-flow HXs were tested to guide the design of the HX to be utilized in the 7 th generation EOIL cavity (CAV7) [Benavides, 2012;Benavides, 2014]. While a diamond shaped tube provided the best characteristics in the original survey [Benavides, 2014], a simple circular tube was found to provide adequate performance and was much more affordable to manufacture. ...
... Classic shock diamonds are present inside the nozzle, Fig. 10; the simulations are in excellent agreement with the experimental data including the predicted total outcoupled power of 200 mW, which is in excellent agreement with the 220 mW measured experimentally. While these simulations were performed for relatively early EOIL experiments, the hardware has since been dramatically improved to attain a gain of 0.30% cm -1 and laser power > 500 W [Benavides, 2012]. Figure 1 shows plasma simulations of the concentric EOIL discharge tubes used in Cav7 [Benavides, 2012], as well as 3D nozzle simulations illustrating the O2(a) concentration and the lasing mode of an earlier Cav5 system [Zimmerman, 2009]. ...
... Influence of molecular oxygen on iodine atoms production in an RF discharge P A Mikheyev 1,2 , N I Ufimtsev 1 , A V Demyanov 3 , I V Kochetov 3 , V N Azyazov 1,2 and A P Napartovich 3 Second, I 2 strongly deactivates I * , leading to energy loss, limiting the optimal [I] and small-signal gain. In the absence of I 2 , the optimal [I] and gain in the active medium could be increased. ...
... Glow discharges had proved to be suitable for atomic iodine production out of different precursor molecules both in dc and pulsed regimes [3][4][5][6][7]. An advantage of using precursors instead of molecular iodine is a small fraction of I 2 at the discharge generator outlet, because it is formed in discharge plasma only through the recombination of iodine atoms. ...
... Diffusion frequencies ( = × v D r 5.78 2 , where D-diffusion coefficient, r-tube radius) for I, O atoms and CH 3 radicals in Ar mixtures were equal to ~300, 800 and 630 s −1 , and in He-900, 1600 and 1400 s −1 , correspondingly. The probability of surface recombination for I atoms, CH 3 and O was chosen to be 1, although there are indications that on a clean surface for I atoms it might be considerably smaller [46] down to 10 −3 ÷ 10 −4 . Also, processes (15)-(16), (62)-(63), (96)-(97) and (99) with participation of CH 2 I 2 ; processes (17)-(21), (68)-(72), (78)-(79) with participation of C 2 H 6 and CH 4 and process (73) were added. ...
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The results of the experiments and modeling of CH3I dissociation in a 40 MHz RF discharge plasma are presented. A discharge chamber of an original design, consisting of quartz tubes between two planar electrodes, permitted us to produce iodine atoms with a number density up to 2 × 1016 cm-3. In this discharge chamber, contrary to the previous experiments with a DC discharge and RF discharge with bare planar electrodes, contamination of the walls of the tubes did not disturb discharge stability, thus increasing iodine production rate. A substantial increase in CH3I dissociation efficiency due to the addition of oxygen into Ar(He) : CH3I mixtures was observed. Complete CH3I dissociation in the Ar : CH3I : O2 mixture occurred at 200 W discharge power, while a fraction of discharge power spent on iodine atoms production at 0.17 mmol s-1 CH3I flow rate amounted to 16%. Extensive numerical modeling showed satisfactory agreement with the experiments and permitted us to estimate a previously unknown rate of constants for the processes: Ar∗ + CH2I2 → Ar + CH2 + I + I - 1.5 × 10-11 cm3 s-1; Ar∗ + CH2I2 → Ar + CH2I+ + I + e - 10-11 cm3 s-1. Also, the cross section for the process CH2I2 + e → CH2 + I + I + e was estimated to be five times smaller than for the analogous process with CH3I.
... Influence of molecular oxygen on iodine atoms production in an RF discharge P A Mikheyev 1,2 , N I Ufimtsev 1 , A V Demyanov 3 , I V Kochetov 3 , V N Azyazov 1,2 and A P Napartovich 3 Second, I 2 strongly deactivates I * , leading to energy loss, limiting the optimal [I] and small-signal gain. In the absence of I 2 , the optimal [I] and gain in the active medium could be increased. ...
... Glow discharges had proved to be suitable for atomic iodine production out of different precursor molecules both in dc and pulsed regimes [3][4][5][6][7]. An advantage of using precursors instead of molecular iodine is a small fraction of I 2 at the discharge generator outlet, because it is formed in discharge plasma only through the recombination of iodine atoms. ...
... Diffusion frequencies ( = × v D r 5.78 2 , where D-diffusion coefficient, r-tube radius) for I, O atoms and CH 3 radicals in Ar mixtures were equal to ~300, 800 and 630 s −1 , and in He-900, 1600 and 1400 s −1 , correspondingly. The probability of surface recombination for I atoms, CH 3 and O was chosen to be 1, although there are indications that on a clean surface for I atoms it might be considerably smaller [46] down to 10 −3 ÷ 10 −4 . Also, processes (15)-(16), (62)-(63), (96)-(97) and (99) with participation of CH 2 I 2 ; processes (17)-(21), (68)-(72), (78)-(79) with participation of C 2 H 6 and CH 4 and process (73) were added. ...
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Results of experiments and modeling of CH3I dissociation in a 40 MHz RF discharge in a discharge chamber of original design to produce iodine atoms for cw oxygen-iodine laser are presented. In experiments a substantial increase in CH3I dissociation efficiency due to addition of oxygen into Ar:CH3I mixture was observed. Complete CH3I dissociation in Ar:CH3I:O2 mixture occurred at 200 W discharge power. Fraction of discharge power spent on iodine atoms production was equal to 16% at 0.17 mmol/s CH3I flow rate. The rate of carbon atoms production as a function of molecular oxygen and water contents in CH3I:Ar mixtures was studied with the help of numerical modeling. It was found that addition of water vapor resulted in increase while addition of molecular oxygen and HI in decrease of the rate of carbon atoms production. Due to diffusion most of carbon atoms had enough time to deposit on the walls of the discharge chamber. However, contrary to the situation in a DC discharge, in the RF discharge accumulation of carbon on the walls of the discharge chamber did not hamper discharge stability and iodine production, as it was observed in our experiments.
... Ionin et al. [Ionin, 2007] and Heaven [Heaven, 2010a] provide comprehensive topical reviews of discharge production of O 2 (a) and various ElectricOIL studies. The highest gain in an ElectricOIL device reported to date is 0.30 % cm -1 [Benavides, 2012], and the highest output power reported is 538 W [Benavides, 2012]. ...
... Ionin et al. [Ionin, 2007] and Heaven [Heaven, 2010a] provide comprehensive topical reviews of discharge production of O 2 (a) and various ElectricOIL studies. The highest gain in an ElectricOIL device reported to date is 0.30 % cm -1 [Benavides, 2012], and the highest output power reported is 538 W [Benavides, 2012]. ...
... Some trade studies used to develop heat-exchangers for ElectricOIL are summarized in [Woodard, 2011] and . The design used in Cav7 experiments is reported in [Benavides, 2012]. ...
Conference Paper
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Over the last decade new advanced gas lasers have emerged as possible candidates for high power laser systems that may supplant more conventional chemical and gas laser systems. Among these are the electric oxygen-iodine laser (ElectricOIL), the diode pumped alkali laser (DPAL), the exciplex pumped alkali laser (XPAL), and the optically pumped metastable rare gas laser. In this paper we will primarily focus on the ElectricOIL and XPAL systems, and discuss some of the recent experiments and modeling of these systems. © 2012 by the authors. Published by the American Institute of Aeronautics and Astronautics, Inc.
... Experiments [1] with Electric Oxygen-Iodine Laser (ElectricOIL) heat exchanger technology have demonstrated improved control of oxygen atom density and thermal energy, with minimal quenching of O 2 (a 1 ), and increasing small signal gain from 0.26% cm -1 to 0.30% cm -1 . Heat exchanger technological improvements were achieved through both experimental and modeling studies, including estimation of O 2 (a 1 ) surface quenching coefficients for select ElectricOIL materials downstream of a radio-frequency discharge-driven singlet oxygen generator. ...
... Ionin [16] and Heaven [17] provide comprehensive topical reviews of discharge production of O 2 (a) and various ElectricOIL studies. Currently, the highest reported peak gain and laser power in an ElectricOIL device are 0.30% cm −1 and 538 W, respectively [1] . ...
... Thinner walls lead to greater temperature gradients, yielding comparable bulk flow temperature reduction with less surface area (better preserving the O 2 (a) population). The fundamental goal of these investigations was to define the STER-7 geometry for the 7 th generation ElectricOIL cavity [1] (CAV7). ...
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... %/cm were previously established and implemented in the development of a 7 th generation laser cavity denoted "Cav7". In this paper, the authors report on design improvements leading to the demonstration of the Cav7 ElectricOIL device having a 5-fold improvement in outcoupled laser power with only a 3-fold increase in device size [Benavides, 2012]. ...
... Some trade studies used to develop heat-exchangers for ElectricOIL are summarized in [Carroll, 2011] and [Zimmerman, 2009]. The design used in Cav7 experiments is altered from the staggered-tube device used for Cav6 [Carroll, 2011]; the new HX having less surface area to reduce O 2 (a) loss, better optimized tube spacing to further reduce pressure loss, and more even coolant distribution to maximize temperature reduction [Benavides, 2012]. ...
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... The most common application of a DBD is ozone production [17,18]. DBD was also studied for plasma assisted combustion [19], and a radio frequency DBD-even for singlet oxygen [20] and iodine atoms [21] production for oxygeniodine laser. ...
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... For the typical post-discharge conditions37 : [He]= 9×10 17 cm -3 , [O 2 ]= 2.5×10 17 cm -3 , [O]=5×10 15 cm -3 , [O 2 (a)]=3×10 16 cm -3 , T=550 K the terms in the denominator satisfy the oxygen quenching rate in process (3) is limited by O 3 (υ) formation rate in the three-body recombination process (2). This is the reason way the authors of Ref. 15 was inclined to conclude that the O 2 (a 1 Δ) deactivation in the O/O 2 /O 2 (a 1 Δ) mixture is a three-body process. ...
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Herein the authors report on the demonstration of an 87% enhancement in cw laser power on the 1315 nm transition of atomic iodine via a 100% increase in the resonator mode volume. O 2 ( a 1 Δ ) is produced by a single rf-excited electric discharge sustained in an O 2 – He – NO gas mixture flowing through a rectangular geometry, and I ( P 2 1 / 2 ) is then pumped using energy transferred from O 2 ( a Δ 1 ) . A total laser output power of 102.5 W was obtained using a Z-pass resonator configuration.
Article
We describe several diode laser-based instruments that can detect important species in chemical oxygen iodine lasers (COIL). Species detected include: water vapor, atomic iodine, and ground state oxygen. The sensors allow non-intrusive, real-time measurements from which one can determine small signal gain and the singlet delta oxygen yield. The water vapor concentrations can also be continuously monitored. The sensitivities of the sensors are sufficient for all the conditions found in typical COIL devices. The room temperature diode lasers are miniature and fiber coupled. Data for all three species are presented.
Article
Recent investigations of an electric oxygen-iodine laser system have shown that computational modeling overpredicts the experimentally measured power output for similar gain conditions. This discrepancy is potentially due to an unknown reaction that competes with the forward pumping of I�2P1/2� by O2�a 1��. Measurements of gain recovery downstream of an operating laser cavity were performed. Modeling of this experiment shows that reducing the forward pumping rate by an effective factor of approximately 4 to simulate a competing mechanism results in the computational modeling matching the experimental gain recovery measurements, and in improved agreement between the measured and modeled laser power extraction.
Article
This is an overview of the development of Chemical Oxygen-Iodine Laser (COIL) technology in the United States. Key technical developments will be reviewed, beginning in 1960 and culminating in 1977 with the first COIL lasing demonstration at the Air Force Weapons Laboratory (now the Phillips Laboratory). The discussion will then turn to subsonic laser development, supersonic lasing demonstration and efficiency improvements, and finishing with a brief discussion of some spin off COIL technologies. Particular emphasis will be placed on how the O2 (1(Delta) ) generator and O2-I2 mixing nozzle technologies evolved.
Article
In this paper, we report on studies of a continuous-wave laser at 1315 nm on the I(2 P 1 2) I(2 P 3 2) transition of atomic iodine where the O 2 (1 1) used to pump the iodine was produced by a radio frequency excited electric discharge. The electric discharge was sustained in He–O 2 and Ar–O 2 gas mix-tures upstream of a supersonic cavity which is employed to lower the temperature of the continuous gas flow and shift the equilib-rium of atomic iodine in favor of the I(2 P 1 2) state. The results of experimental studies for several different flow conditions, dis-charge arrangements, and mirror sets are presented. The highest laser output power obtained in these experiments was 520 mW in a stable cavity composed of two 99.995% reflective mirrors. Index Terms—Chemical oxygen–iodine laser (COIL), electric discharge oxygen–iodine laser, electriCOIL, radio frequency (RF) excitation of oxygen, singlet-delta oxygen.
Article
Herein the authors report on the demonstration of gain and a continuous-wave laser on the 1315 nm transition of atomic iodine using the energy transferred to I(2P1/2) from O2(a1Δ) produced by a radio-frequency-excited electric discharge sustained in a dry air-He–NO gas mixture. Active oxygen and nitrogen species were observed downstream of the discharge region. Downstream of the discharge, cold gas injection was employed to raise the gas density and lower the temperature of the continuous gas flow. Gain of 0.0062% cm−1 was obtained and the laser output power was 32 mW in a supersonic flow cavity.
Article
cw laser action was achieved on the 2P1/2→2P3/2 transition of the iodine atom by energy transfer from the 1Δ metastable state of O2. The excited oxygen was generated chemically by flowing chlorine gas through a basic solution of 90% H2O2. The effluent from the oxygen generator was mixed with molecular iodine at the entrance of a longitudinal flow laser cavity where the I2 was dissociated by a small amount of O2(1Σ) that was present in the flow due to energy pooling processes. The measured output power was greater than 4 mW.
Article
Herein the authors report on the demonstration of a 50% enhancement in gain and 38% enhancement in continuous-wave laser power on the 1315 nm transition of atomic iodine through the addition of a secondary discharge to predissociate the molecular iodine in an electric oxygen-iodine laser. In the primary discharge the O2(a 1Δ) is produced by a radio-frequency-excited electric discharge sustained in an O2–He–NO gas mixture, and I(2P1/2) is then pumped using energy transferred from O2(a 1Δ). A gain of 0.10% cm−1 was obtained and the total laser output power was 6.2 W.
Article
Herein the authors report on the demonstration of a continuous-wave laser in subsonic flow on the 1315 nm transition of atomic iodine using the energy transferred to I() from O2(a ) produced by a radio-frequency-excited electric discharge. The electric discharge was sustained in an O2–He–NO gas mixture. Downstream of the discharge, cold gas injection was employed to raise the gas density and lower the temperature of the continuous gas flow to shift the equilibrium of atomic iodine in favor of the I() state. The laser output power was 540 mW in a stable cavity with two 99.993% reflective mirrors.
Article
Singlet delta oxygen (SDO) yield, small signal gain, and output power have been measured in a scaled electric discharge excited oxygen–iodine laser. Two different types of discharges have been used for SDO generation in O2–He–NO flows at pressures up to 90 Torr, crossed nanosecond pulser/dc sustainer discharge and capacitively coupled transverse RF discharge. The total flow rate through the laser cavity with a 10 cm gain path is approximately 0.5 mole s−1, with steady-state run time at a near-design Mach number of M = 2.9 of up to 5 s. The results demonstrate that SDO yields and flow temperatures obtained using the pulser-sustainer and the RF discharges are close. Gain and static temperature in the supersonic cavity remain nearly constant, γ = 0.10–0.12% cm−1 and T = 125–140 K, over the axial distance of approximately 10 cm. The highest gain measured is 0.122% cm−1 at T = 140 K. Positive gain measured in the supersonic inviscid core extends over approximately one half to one third of the cavity height, with absorption measured in the boundary layers near top and bottom walls of the cavity. Laser power has been measured using (i) two 99.9% mirrors on both sides of the resonator, 2.5 W, and (ii) 99.9% mirror on one side and 99% mirror on the other side, 3.1 W. Gain downstream of the resonator is moderately reduced during lasing (by up to 20–30%) and remains nearly independent of the axial distance, by up to 10 cm. This suggests that only a small fraction of power available for lasing is coupled out, and that additional power may be coupled in a second resonator. Preliminary laser power measurements using two transverse resonators operating at the same time (both using 99.9–99% mirror combinations) demonstrated lasing at both axial locations, with the total power of 3.8 W.
Article
Chemical oxygen-iodine lasers are unique in their ability to generate high-power beams with near diffraction limited beam quality. The operating wavelength, 1.315 µm is readily transmitted by the atmosphere and compatible with fiber optics beam delivery systems. However, applications of the laser are severely limited by logistical problems associated with the complex chemistry used to power the device. Electrical or microwave discharge excitation of oxygen-iodine lasers offers an attractive alternative that eliminates the chemical power generation problems and has the possibility of closed-cycle operation. A discharge oxygen-iodine laser was first demonstrated in 2005. Since that time the power of the device has been improved by a factor of 400 and much has been learned concerning the physics and chemistry of the discharge driven system. Although our current understanding of the chemical kinetics is incomplete, parametric studies of laser performance show considerable promise for further scaling. This article reviews the basic principles of the discharge oxygen iodine laser, summarizes the most recent advances, and outlines some of the unresolved questions regarding the production and removal of excited species in the gas flow.
Article
Chemical oxygen-iodine lasers (COIL) are attractive for diverse industrial applications because they are capable of high efficiency, high power operation, and because the 1.315 μ m wavelength can be transmitted through fiber optics and couples efficiently with most metals. Conventional COILs are pumped with O 2(1 Δ ) that is generated by reaction of Cl 2 in a basic H 2 O 2 solution. Current trends in pumping COILs involve producing the O 2(1 Δ ) in electric discharges, thereby circumventing the hazards, complexity, and weight associated with pumping and storing caustic liquids. In this work, we have investigated the scaling of O 2(1 Δ ) yields with specific energy deposition in He / O 2 mixtures in flowing radio frequency (rf) discharges at pressures of a few to tens of Torr using a global plasma kinetics model. We found that O 2(1 Δ ) yield increases nearly linearly with specific energy deposition in O 2 molecules up to a few eV per molecule, with yields peaking around 30% by 5–8 eV . Further increases in specific energy deposition serve only to increase O 2 dissociation and gas heating, thereby reducing the O 2(1 Δ ) yield. We also found that variations in peak yields at a given specific energy de- position are caused by secondary effects resulting from dilution, pressure, and power level. We show that these secondary effects alter the O 2(1 Δ ) yield by shifting the O 2(1 Σ )/ O 2(1 Δ ) ratio.
Article
In an electric discharge oxygen-iodine laser, laser action at 1315 nm on the I (2P1/2)→ I (2P3/2) transition of atomic iodine is obtained by a near resonant energy transfer from O 2(a 1Δ) which is produced using a low-pressure electric discharge. The discharge production of atomic oxygen, ozone, and other excited species adds higher levels of complexity to the postdischarge kinetics which are not encountered in a classic purely chemical O 2(a 1Δ) generation system. Mixing effects are also present. In this paper we present postdischarge modeling results obtained using a modified version of the BLAZE-II gas laser code. A 28 species, 105 reaction chemical kinetic reaction set for the postdischarge kinetics is presented. Calculations were performed to ascertain the impact of a two stream mixing mechanism on the numerical model and to study gain as a function of reactant mass flow rates. The calculations were compared with experimental data. Agreement with experimental data was improved with the addition of new kinetics and the mixing mechanism.
Article
Laser action at 1315 nm on the I (2P1/2)→ I (2P3/2) transition of atomic iodine is conventionally obtained by a near-resonant energy transfer from O 2(a1Δ) which is produced using wet-solution chemistry. The difficulties in chemically producing O 2(a1Δ) has motivated investigations into purely gas phase methods to produce O 2(a1Δ) using low-pressure electric discharges. In this letter, we report on the demonstration of a continuous-wave laser on the 1315 nm transition of atomic iodine where the O 2(a1Δ) used to pump the iodine was produced by a radio-frequency-excited electric discharge. The electric discharge was sustained in a He / O 2 gas mixture upstream of a supersonic cavity which is employed to lower the temperature of the continuous gas flow and shift the equilibrium of atomic iodine in favor of the I (2P1/2) state. The laser output power was 220 mW in a stable cavity composed of two 99.99% reflective mirrors.
Article
Laser action at 1315 nm on the I(2P1/2)→I(2P3/2) transition of atomic iodine is conventionally obtained by a near-resonant energy transfer from O 2(a1Δ) , which is produced using wet-solution chemistry. The system difficulties of chemically producing O 2(a1Δ) has motivated investigations into gas phase methods to produce O 2(a1Δ) using low-pressure electric discharges. In this letter we report on positive gain on the 1315 nm transition of atomic iodine where the O 2(a1Δ) was produced in a flowing electric discharge. The electric discharge was followed by a continuously flowing supersonic cavity that was necessary to lower the temperature of the flow and shift the equilibrium of atomic iodine more in favor of the I (2P1/2) state. A tunable diode laser system capable of scanning the entire line shape of the (3,4) hyperfine transition of iodine provided the measurements of gain.
Article
Laser oscillation at 1315 nm on the I(2P1/2)-->I(2P3/2) transition of atomic iodine has been obtained by a near resonant energy transfer from O2(a1Delta) produced using a low-pressure oxygen/helium/nitric oxide discharge. In the electric discharge oxygen-iodine laser (ElectricOIL) the discharge production of atomic oxygen, ozone, and other excited species adds levels of complexity to the singlet oxygen generator (SOG) kinetics which are not encountered in a classic purely chemical O2(a1Delta) generation system. The advanced model BLAZE-IV has been introduced to study the energy-transfer laser system dynamics and kinetics. Levels of singlet oxygen, oxygen atoms, and ozone are measured experimentally and compared with calculations. The new BLAZE-IV model is in reasonable agreement with O3, O atom, and gas temperature measurements but is under-predicting the increase in O2(a1Delta) concentration resulting from the presence of NO in the discharge and under-predicting the O2(b1Sigma) concentrations. A key conclusion is that the removal of oxygen atoms by NOX species leads to a significant increase in O2(a1Delta) concentrations downstream of the discharge in part via a recycling process; however, there are still some important processes related to the NOX discharge kinetics that are missing from the present modeling. Further, the removal of oxygen atoms dramatically inhibits the production of ozone in the downstream kinetics.
Palla received the M.S. degree in aerospace engineering with the University of Illinois at Urbana-Champaign He is currently a Senior Physicist with CU Aerospace
  • D Andrew
Andrew D. Palla received the M.S. degree in aerospace engineering with the University of Illinois at Urbana-Champaign, Urbana, in 2004. He is currently a Senior Physicist with CU Aerospace, Champaign, IL.
Benavides is a Ph.D. student in aerospace engineering with the University of Illinois at Urbana-Champaign, Urbana, with an expected graduation date of May 2012. He is currently a Senior Engineer with CU Aerospace
  • F Gabriel
Gabriel F. Benavides is a Ph.D. student in aerospace engineering with the University of Illinois at Urbana-Champaign, Urbana, with an expected graduation date of May 2012. He is currently a Senior Engineer with CU Aerospace, Champaign, IL.
M'98–SM'07) received the Ph.D. degree in aerospace engineering with the University of Illinois at
  • David L Carroll
David L. Carroll (M'98–SM'07) received the Ph.D. degree in aerospace engineering with the University of Illinois at Urbana-Champaign, Urbana, in 1992.
Day received the M.S. degree in aerospace engineering with the University of Illinois at Urbana-Champaign
  • T Michael
Michael T. Day received the M.S. degree in aerospace engineering with the University of Illinois at Urbana-Champaign, Urbana, in 2011.
King received the M.S. degree in aerospace engineering with the University of Illinois at Urbana-Champaign, Urbana, in 1999. He is currently the Laboratory Manager and a Senior Engineer with CU Aerospace
  • M Darren
Darren M. King received the M.S. degree in aerospace engineering with the University of Illinois at Urbana-Champaign, Urbana, in 1999. He is currently the Laboratory Manager and a Senior Engineer with CU Aerospace, Champaign, IL.
Carroll is a Fellow of the American Institute of Aeronautics and Astronautics (AIAA) and the current Chair of the AIAA Plasmadynamics and Lasers Technical Committee
  • Dr
Dr. Carroll is a Fellow of the American Institute of Aeronautics and Astronautics (AIAA) and the current Chair of the AIAA Plasmadynamics and Lasers Technical Committee.
Zimmerman received the Ph.D. degree in aerospace engineering with the University of Illinois at Urbana-Champaign He is currently a Staff Scientist with CU Aerospace
  • W Joseph
Joseph W. Zimmerman received the Ph.D. degree in aerospace engineering with the University of Illinois at Urbana-Champaign, Urbana, in 2010. He is currently a Staff Scientist with CU Aerospace, Champaign, IL.
He was a Professor and the Head of aerospace engineering with the University of Illinois at Urbana-Champaign, Urbana, from 1988 to 1999. He is currently a Professor Emeritus with the University of Illinois at Urbana- Champaign and the Chairman of CU Aerospace
  • C Wayne
Wayne C. Solomon received the Ph.D. degree in chemistry with the University of Oregon, Eugene, in 1963. He was a Professor and the Head of aerospace engineering with the University of Illinois at Urbana-Champaign, Urbana, from 1988 to 1999. He is currently a Professor Emeritus with the University of Illinois at Urbana- Champaign and the Chairman of CU Aerospace, Champaign, IL.
Woodard is a Ph.D. student in aerospace engineering with the University of Illinois at Urbana-Champaign, Urbana, with an expected graduation date of
  • S Brian
Brian S. Woodard is a Ph.D. student in aerospace engineering with the University of Illinois at Urbana-Champaign, Urbana, with an expected graduation date of December 2011.
Observations of gain on the ${rm I}(^{2}!P_{1/2}rightarrow,^{2}!P_{3/2})$ transition by energy transfer from ${rm O}_{2}(a^{1}Delta_{g})$ generated by a microwave discharge in a subsonic-flow reactor
  • W T Rawlins
  • S Lee
  • W J Kessler
  • S J Davis