that is the nominal composition of hydrogen and carbon in the naptha, Hydrogen 52%(mol%) and carbon 0.84%(mol%)
That is nonsens.
firstly i converted the 41100 metric tons/year of hydrogen produced to kmol/hr by dividing by molar mass of hydrogen
Note that the hydrogen product is only 97.4 mol% so its MW is much higher than that of pure hydrogen.
1. First of all: what you call primary reformer is normally called Prereformer.
The primary reformer is the reformer heater (which you seem to call secondary reformer)
A secondary reformer could be an autothermal reformer (using air or pure oxygen) located downstream the reformer heater.
In the prereformer all C11H24 will indeed be converted into CO2 plus CO plus CH4 plus H2 but amounts of each depend on equilibrium Kp's (and approach to equilibrium ATE for methanation and watergas shift reactions) at prereformer outlet T and P.
2. Carbon in the naphtha will obviously be the C11 part of the C11H24
3. Use Kp's and ATE's for both the methanation and watergas shift equilibria at heater outlet P and T (like for prereformer)
4. Normally steam is added at prereformer feed and more steam downstream prereformer before reformer heater. Different licensors will use different S/C ratios, but I suggest that for (very) heavy naphtha you use S/C ratios of at least 2.5 for prereformer inlet, as well as for reformer heater inlet.
Your questions make me wonder: are you a chemical engineer or a mechanical engineer?
Edited by PingPong, 02 October 2014 - 09:07 AM.