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64   G a s , C h e m i c a l , a n d F r e e - E l e c t r o n L a s e r s     Chemical Lasers    65


                      Thus, current activity in HF and DF chemical lasers is limited to low-
                      power laboratory devices and specialty applications, which typically
                      use electrical discharge, rather than combustion, to dissociate SF  to
                                                                             6
                      produce fluorine atoms and which range in power from tens of watts
                      to a few hundred watts.

                 3.4  Chemical Oxygen Iodine Laser (COIL)

                      The possibility of making a COIL device was first suggested by
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                      Derwent and Thrush  in 1971. The first lasing demonstration was
                      made by McDermott and his team at the Air Force Weapons Lab
                                     13
                      (AFWL)  in  1978.   Truesdell,  Helms,  and  Hager   summarized
                                                                  14
                      development efforts within the United States through 1995. Tech-
                      nology improvements and scaling to large devices have continued
                      at a variety of sites.
                         COIL devices are based on a very different chemistry from HF and
                      DF lasers. Figure 3.20 shows a simplified block diagram of the opera-
                      tional approach. First, chlorine gas reacts with liquid basic hydrogen
                      peroxide (BHP) in a gas-liquid reaction. The reaction then produces
                      electronically excited singlet delta oxygen, which has a very long life-
                      time as compared with most electronically excited states. The reactor
                      is denoted a singlet delta oxygen generator (SOG). Next, the excited
                      oxygen,  along  with  a  suitable  diluent,  is  transported  to  supersonic
                      expansion nozzles, which mix the oxygen with molecular iodine and
                      a suitable carrier gas. The singlet delta oxygen chemically dissociates
                      the molecular iodine to produce atomic iodine, which has electronic
                      states that favor the resonant transfer of energy from the singlet delta
                      oxygen to the iodine. The resultant gain allows lasing on an atomic
                      iodine transition. Typically, the ratio of oxygen to iodine atoms is rela-
                      tively large, and many energy transfers occur per iodine atom until
                      the singlet delta fraction is sufficiently depleted. As the block diagram
                      in Fig. 3.20 shows, a practical device must also include provisions to
                      circulate the BHP, remove the reaction heat, and recover pressure to
                      ambient conditions.


                      3.4.1  Energy Levels
                      The lasing species in COIL devices is the iodine atom. In contrast to
                      most other chemical lasers, the transition energy levels are electronic
                      rather than molecular. The lasing transition is a magnetic dipole tran-
                      sition  between  two  spin  orbit  terms  of  the  ground  state  5 P 1/2   →
                                                                         2
                       2
                      5 P 3/2 .  Because  this  transition  is  forbidden,  it  has  a  relatively  long
                      radiative lifetime of approximately 125 milliseconds (ms). The upper
                      level  is  split  into  two  hyperfine  levels—total  angular  momentum
                      quantum  numbers,  F  =  2  and  3.  The  lower  level  is  split  into  four
                      hyperfine levels, F = 1, 2, 3, and 4. Associated degeneracies are 2F + 1.
                      The energy levels are shown schematically in Fig. 3.21, in which the
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