Questions and Answers For Primary Reformer
Questions and Answers For Primary Reformer
Q2. What do you consider a good TWT distribution, do you have some advice for balancing
a reformer and are there any instruments other than a pyrometer to measure TWT?
A2. Most operating plants can achieve a tube wall temperature spread of less than
100°C/180°F. Most plants use handheld IR pyrometers to measure the TWT, although
there is increasing use of thermal imaging cameras. Fixed installed cameras are also
now available for continuous monitoring of the reformer TWT's. There are also pseudo
contact pyrometer's, such as Johnson Matthey's Gold Cup pyrometer, that can provide
a more accurately measure of TWT for troubleshooting requirements. For effective
balancing of the reformer it is important to ensure your pyrometer is routinely
calibrated, TWT measurements are recorded, only small step changes are made to the
reformer and sufficient time is given to the reformer to re-equilibrate before re-
assessing the TWT's and making the next change. Providing appropriate training and
guidance to your operators for this purpose is important.
Q3. Does low rate operation affect the location of carbon formation and if there is carbon,
what should we look for?
A3. The carbon formation region may move slightly towards the tube inlet at low rates,
however generally carbon is still most probable at the 20-40% zone of the tube length.
Whenever the reformer is operated at abnormal operating conditions, it is advisable to
make frequent visual assessment of the reformer tubes. Attention should be paid to
signs of flame impingement, hot zones in the reformer and signs of hot spots/patches.
Q4. What is a hotspot and can you tell the difference between hot spots caused by poisoning
and carbon formation?
A4. Hot spots caused by poisoning and carbon formation can appear very similar in
appearance. Any occurrence requires a root cause analysis. Slip of sulphur from the
purification section should be conducted to assess for poisoning and a review of
operating data to check for accidental operation at low steam to carbon rations.
Q5. What factors affect the methane slip, how do you calculated approach to equilibrium
(ATE) and how does low rates affect conversion?
A5. Methane slip is a function of feed flow, feedstock composition, temperature, pressure,
catalyst activity and S:C ratio. ATE is calculated by measuring the outlet methane slip
and comparing the catalyst exit temperature to the equilibrium temperature for the
same methane slip. At fixed operating conditions, the ATE is an indication of the catalyst
activity.
1/3
reformers complex inlet and outlet headers are required in order to maintain uniform
distribution of process gas to the tubes, fuel and air to the burners and to collect the
flue gas across rows of tunnels. In a side fired or terrace wall reformer the challenge
is to maintain uniform process gas distribution between the two cells and along the tube
row, which would have a larger number of tubes per row than an equivalent capacity
top fired reformer. A side fired reformer also has more burners that need to be
managed, with the added complexity of a varying draft pressure in the radiant section
due to flue gas upwards flow.
Q7. Why does the flue gas go downwards in a top fired reformer and how can you tell if you
have maldistribution of the flue gas?
A7. The flue gas in a top fired reformer flows downwards as it is designed with flue gas
collection tunnels at the floor which remove the flue gas from the radiant box directing
it into the convection system, in which there is an induced draft fan. Mal-distribution
of flue gas can be identified by observing the direction and turbulence of the flames and
may be observed from a pattern in the TWT's measured. A dry powder injection test
can also be conducted through the burner ignition port to better observe the flow
direction of the flue gas.
Q8. How is fuel affected at low rates and how should burners be managed?
A8. Relative heat loss is higher at low rates. As mentioned in the webinar, it can also be
useful to operate at higher S:C ratios and higher excess air ratios at low rates. With
these effects fuel turn down may not be linear to plant load. Trim fuel is always added
to purge gas to maintain steady operating conditions. It is normally preferable to
reduce the fuel pressure to all the burners, rather than isolating individual burners,
however there may be occasions when isolating individual burners is desired, e.g. to
manage a hot tube. Burner operating procedures significantly vary depending on the
burner design and therefore the flexibility in operating modes of the burners should be
discussed with the burner supplier.
Q10. What correlation does the pressure drop have to even distribution of process gas in the
tubes?
A10. During the catalyst loading, the pressure drop across each tube will be checked. A
pressure drop between tubes of ± 5% is normally expected. Often ± 3% can be
achieved especially with semi-automated loading techniques. A high pressure drop
across the reformer during operation is an indication of a restriction in flow. If the
restriction is only within a few of the tubes, then this will cause maldistribution of
process gas.
Q12. Why should S:C ratio be increased at low rates, what is the optimum S:C ratio at low
rates and how long can you operate on steam alone?
A12. The optimum S:C ratio tends to be governed by the flowsheet. Factors include the
balance between conversion, prevention of carbon formation and maximising plant
efficiency. At low rates there is an increased risk of maldistribution of both the process
gas and of the heat distribution in the radiant box. Consequently, increasing S:C ratio
at low rate helps improve the distribution of process gas, aids in preventing high TWTs
and it also increases the margin for carbon formation. Your catalyst supplier can advise
2/3
how long you can operate your reformer catalyst at high S:C, as effects can vary
depending on the catalyst types.
Q14. Why for lower plant rates do you recommend lower system pressure?
A14. Reducing the pressure reduces the gas density, which helps to increase velocity in the
reformer tubes, thus improving heat transfer and gas distribution. It also reduces the
chance of tube damage if overheated.
Q15. How can you determine how much heat loss you have?
A15. The heat loss from the reformer can be calculated by modelling the energy balance
around the unit, which requires the heat input from the fuel, the expected heat demand
from the process and the process conditions. For the calculation of temperature loss at
the outlet of the reformer, it is possible to assume the water gas shift reaction will be
at equilibrium at the exit of the reforming catalyst. Provided you can complete an
accurate heat and mass balance around the reformer, it is possible to calculate the WGS
equilibrium temperature for the wet gas composition. The difference between this
temperature and the measured reformer exit temperature provides the temperature
loss.
Further Information
Please contact your local Johnson Matthey representative for further information or send your
enquiry to [email protected]
All information comprised in or relating to the contents of this report shall be treated by the parties as confidential
and shall not be disclosed to third parties by any party without the prior consent of the other.
The information, data and results contained in this report together with any suggestions, advice and/or
recommendations contained therein (individually and collectively “the Information”) are given in good faith but
Johnson Matthey does not warrant or guarantee the correctness, adequacy or suitability of the Information and
it shall be the sole responsibility of the customer to assess the Information and whether or not to accept, act on
or implement the same. If the customer does elect to do so, then Johnson Matthey shall not have any for any
loss or damage suffered as a result, whether in contract, tort (including negligence) or otherwise (other than
that arising from death or personal injury caused by Johnson Matthey’s negligence).
3/3