Page 176 - Analysis, Synthesis and Design of Chemical Processes, Third Edition
P. 176

It has been proposed that we handle the hydrogen/methane stream in the same manner that we handled the
                    toluene/benzene stream. We recall that the unreacted toluene was separated from the benzene product and
                    then recycled. It is proposed that the methane be separated from the hydrogen. The methane would then
                    become  a  process  by-product  and  the  hydrogen  would  be  recycled.  Discuss  this  proposal  using  the
                    arguments provided in Tables 6.1 and 6.2.


                    To use distillation for the separation of methane from hydrogen, as was used with the toluene/benzene,
                    requires a liquid phase. For methane/hydrogen systems, this requires extremely high pressures together
                    with cryogenic temperatures.


                    If the hydrogen could be separated from the methane and recycled, then the reactor feed would not contain
                    significant quantities of methane, and the large excess of hydrogen could be maintained without the steep
                    cost of excess hydrogen feed. Note that the overall conversion of hydrogen in the process is only 37%,
                    whereas for toluene it is 99%.


                    Alternative separation schemes that do not require a liquid phase (e.g., a membrane separator) should be
                    considered. The use of alternative separation technologies is addressed further in Chapter 12.


                    6.4.2 Evaluation of High-Pressure Phase Separator V-102





                    This  vessel  separates  toluene  and  benzene  as  a  liquid  from  the  noncondensable  gases  hydrogen  and
                    methane. The reactor product is cooled and forms a vapor and a liquid stream that are in equilibrium. The
                    vapor-liquid  equilibrium  is  that  at  the  temperature  and  pressure  of  the  stream  entering  V-102.  From
                    Tables 6.1 and 6.2, we conclude that the lower temperature (38°C) was provided to obtain a liquid phase
                    for  the  vapor-liquid  equilibrium.  The  pressure  was  maintained  to  support  the  formation  of  the  liquid
                    phase.  Because  the  separation  can  be  affected  relatively  easily  at  high  pressure,  it  is  worthwhile
                    maintaining V-102 at this high pressure.


                    6.4.3 Evaluation of Large Temperature Driving Force in Exchanger E-101





                    There  is  a  large  temperature  driving  force  in  this  exchanger,  because  the  heating  medium  is  at  a
                    temperature of approximately 250°C, and the inlet to the exchanger is only 30°C. This is greater than the
                    100°C suggested in Table 6.4. This is an example of poor heat integration, and we will take a closer look

                    at improving this in Chapter 15 (also see the case study presented in Chapter 28).

                    6.4.4 Evaluation of Exchanger E-102





                    Stream 9 is cooled from 654°C to 40°C using cooling water at approximately 35°C. Again this is greater

                    than the 100°C suggested in Table 6.4, and the process stream has a lot of valuable energy that is being
                    wasted. Again, we can save a lot of money by using heat integration (see Chapter 15).

                    6.4.5 Pressure Control Valve on Stream 8
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