Page 410 - Instrumentation Reference Book 3E
P. 410

Detectors 393
             reaction  is uncertain,  but  it  is  believed  that  the   technique  is  the  basis  of  the ultrasonic detector
             excitation energy for the SZ + S;  transition may   (Figure  18.12).  A  quartz  crystal  transducer
             come from -the formation of molecular hydrogen   located at one end of the sample cell sound tube
             or water in the flame, according to the reactions   acts as the emitter, and an identical crystal located
                 H + H + S2  4 + H2  (4.5 eV)         at the  other  end  of  the  sound  tube  acts  as  the
                             S"
                                                      receiver.  To  obtain  efficient  transfer  of  sound
                 H + OH + S? +*S;  + H20 (5.1 eV)
                                                      energy between the gas and the transducers, the
             As the excited SZ. molecule reverts to the ground   detector must be operated at above atmospheric
             state  it  emits  a  series  of  bands  in  the  range   pressure, and the gas in the cell is typically regu-
             300-450 nm, with the most intense bands at 384.0   lated  to  1 to 7 bar gauge depending on the gas.
             and 394.1 nm. The 384.0 nm emission is monitored   The phase shift of the sound signal traversing the
             by the photomultiplier tube.             cell between the emitter and receiver is cornpared
               The FPD is highly selective and sensitive, but   to a reference signal to determine the change in
             the response  is  not  linearly proportional to the   speed of sound in the detector.
             mass-flow rate of the sulfur compound. Instead,   The detector is most often used in gas chroma-
             the relationship is given by:            tography.  It  has  a  universal  response,  and  the
                                                      output signal is proportional to the difference in
                                                      molecular  weight  between  the  gaseous  species
             where Is2 is the observed intensity of the emission   forming  the  binary  mixture.  When  used  as  a
             (photoincltiplier tube output), [SI is the mass-flow   gas-chromatographic detector  it has  good  sensi-
             rate of su!fur  atoms (effectively the concentration   tivity  (10-9-10-'0g)  and  a  wide  linear  dynamic
             of  the  sulfur  compound)  and  i?  is  a  constant,   range (lo6), and allows a wide choice of  carrier
             found  to  be  between  1.5  and  2,  depending  on   gas.  However,  precise  temperature  control  is
             flame conditions.  Commercial analyzers employ-   required,  and the electronic circuitry is complex.
             ing the FPD often incorporate a linearizing circuit   It may be a useful alternative where flames can-
             to give an  output which is directly proportional to   not be used, or where a katharorneter would not
             sulfur mass-flow. The detector response is limited   respond to ail components in a mixture.
             to two or three orders of magnitude.
               The FPD is highly selective, sensitive (lO-"g),   18.3.8  Catalytic detector (pellistor)
             and relatively simple, but has an extremely non-
             linear response. It is used in gas chromatography   Catalytic  gas  detectors  operate  by  measuring
             and in sulfur analyzers.                 the heat  output resulting from the catalytic oxi-
                                                      dation  of  flammable  gas  molecules  to  carbon
                                                      dioxide  and water  vapor  at  a  solid surface.  By
                                                      use  of  a  catalyst, the  temperature  at  which  the
             18.3.7  Ultrasonic detector
                                                      oxidation takes place is much reduced compared
             The velocity of sound in a gas is inversely propor-   with  gas  phase  oxidation.  The  catalyst  may  be
             tional to the square root of its molecular weight.   incorporated into a solid state sensor containing
             By measuring the speed of sound in a binary gas   an  electrical  heater  and  temperature-sensing
             mixture, its composition can be deduced, and this   device. A  stream  of  sample  gas  is  fed  over  the


                  From drive                                    End  To  receiver
                 oscillator               Gasout   Cell body    ca(3   amplifier
                                                   ,













                                           Gasin   Spring
               Arrows show gas flow                     O-ring
             Figure 18.12  Ultrasonic detector.
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