12 - Reforming Catalyst Regeneration
12 - Reforming Catalyst Regeneration
12 - Reforming Catalyst Regeneration
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IV - OXYCHLORINATION - CALCINATION.........................................................................................8
V - CATALYST REDUCTION.............................................................................................................11
VI - SULFURIZATION..........................................................................................................................12
OPERATIONS COMMENTS
• Reaction section is DECOMPRESSED Gaseous phase consisting of hydrogen and hydrocarbons is eliminated. It is
replaced by nitrogen gas (inert gas) so that the combustion phase can be
• NITROGEN scavenging to PURGE; compressions; decompressions carried out by introducing a controlled amount of air in the nitrogen
OPERATIONS COMMENTS
• Reaction section is isolated by blind flanges from any circuits that may • Safety aspect
contain hydrocarbons
• Combustion air injection line is prepared at the recycle compressor intake • Circuits required for the different regeneration phases are prepared
• Sampling devices are prepared • Sampling devices and analyzers (used to check that operations take
place properly) are installed
• Oxygen analyzer is installed
• Stocks of chemicals and materials (used during regeneration) are
checked
• Pump and chlorinated compound (DCP) injection lines are checked
(see figure in Appendix)
• Anticorrosion loop (ACL) is prepared
OPERATIONS COMMENTS
D CH 1084 A
x x • Because of the platinum present on the catalyst, no carbon monoxide (CO)
CHx + (
4
+ 1) O2 CO2 + 2
H 2O
is formed when the carbon in the coke is burned (platinum catalyzes the
formation of CO2 even in the presence of very little oxygen)
1 1
H + 4 O2 2 H 2O + 28600 kcal/kg
1 kg 8 kg 9 kg of burned hydrogen
The heat released by coke combustion is considerable. This heat flow must
be eliminated while combustion is taking place in order to limit catalyst bed
temperature increase.
OPERATIONS COMMENTS
OPERATIONS COMMENTS
• ANTICORROSION LOOP (ACL) is activated at about 300°C. Caustic is • Corrosion is limited in the cold part of the unit (air coolers, flash drum):
circulated upstream from the air coolers toward the flash drum:
Chlorine is necessarily elutriated from the catalyst by the water formed
– monitor its flow rate when the hydrogen in the coke burns. Elution releases hydrogen chloride
gas (HCl) in the recycle gas. As a result, a hydrochloric acid solution is
– adjust caustic makeup depending on the pH indication in the flash formed which is particularly corrosive for metallic materials as soon as the
drum water condenses.
This corrosion is limited by the caustic in the ACL neutralizing the acid
solution. The reaction is as follows:
If the pH drops, then the caustic makeup in the anticorrosion loop must be
increased to offset caustic consumption. The drum level is maintained by
purging. Active caustic concentration is checked by monitoring the pH in
B101 (should be slightly greater than 7).
OPERATIONS COMMENTS
• Pure DCP injection is started at approximately 350°C to keep a molar ratio: • The recycle gas is saturated in water. Chlorine elution from the catalyst is
offset by DCP injection so as to keep an optimum chlorine rate in the
H 2O catalyst. Additionally, chlorine injection during combustion helps keep the
HCI = 20 platinum from being sintered during combustion as shown in Figure 1.
Platinum dispersion in air decreases very quickly with time when no chlorine
in the reaction section during combustion is injected. However, it remains constant and even increases slightly if
chlorine is injected in adequate amounts to keep the chlorine content in the
catalyst at around 1% mass.
• Air injection is started at 400°C • Combustion usually starts as soon as the O2 concentration reaches 0.1%
volume in the gases at the inlet to the first reactor
• Oxygen concentration is monitored at reaction section inlet and outlet. CO2
concentration is monitored at the outlet • Combustion process can be monitored
• Maximum of 0.5 to 0.6% volume of O2 at the reaction section inlet • Heat release is limited
Air flow rate is adjusted so that: • OVERHEATING should be prevented, even locally
t of the bed does not exceed 50°C When the alumina in the catalyst is raised to a high temperature in the
presence of steam, it changes its structure and then loses its catalytic
or properties. In particular, its surface area decreases quite considerably if the
temperature rises as shown in Figure 4.
maximum reactor outlet t does not exceed 450°C
with 0.1% O2 T of 10°C OVERHEATING DURING COMBUSTION
MEANS IRREMEDIABLE LOSS OF
• Combustion is monitored reactor by reactor ALUMINA SURFACE AREA
OPERATIONS COMMENTS
H 2O • Chlorine rate is held on the catalyst during combustion to keep the platinum
• DCP injection is adjusted to keep the HCl ratio at a value of 20 from being sintered
• When the t of the last reactor becomes zero and the oxygen percentages
• End of the initial combustion phase of the reaction section inlet and outlet remain identical, the primary
combustion phase can be considered completed
• Reactor inlet temperature is raised to 510°C , with 0.5% volume O2 • Combustion may be resumed. If t rises, air is cut off to prevent any
overheating
• Monitoring: reactor outlet t 520°C max
H 2O
• HCl ratio is held = 20
• End of secondary combustion • The coke elimination phase is theoretically completed if the temperature
remains stable at 510°C with 0.6 to 0.8% volume of oxygen
OPERATIONS COMMENTS
OPERATIONS COMMENTS
COOLING • The unit is cooled down so that it can be inerted with nitrogen
OPERATIONS COMMENTS
• NITROGEN scavenging PURGE, compressions, decompressions until there • The inert atmosphere is implemented in order to be able to introduce the
is 0.3% O2 in the nitrogen hydrogen required for the reduction phase
• Pressure should not be lowered too much (1.7 bar minimum) • Hydrocarbons that may be trapped in the insulating refractory of the reactors
should not be desorbed. The presence of these hydrocarbons is highly
Pressure surges should be avoided detrimental to the catalyst during the reduction phase which follows
OPERATIONS COMMENTS
D CH 2057 A
• Pure hydrogen must be used for this reduction, since some of the reduced
platinum is extremely reactive during the reaction and will transform any
hydrocarbon into coke. As a result, reforming hydrogen must therefore not
• Pure, perfectly dry, electrolytic hydrogen is introduced be used for start-up and hydrocarbons must not be released from the
refractory of the reactors by pressure surges
• The indications of the recycle flow meter are corrected. The recycle
• The compressor is started up compressor is checked to be sure it is operating outside its surging zone
• The furnaces are lit, the temperature is raised to 485°C • Figure 3 shows there is an optimum reduction temperature that yields
maximum dispersion of metallic platinum. If the temperature is too low, only
part of the platinum is reduced. On the other hand, too high a temperature
promotes sintering of the metal, thereby reducing dispersion
• The temperature is held at 485°C for 4 hours
• Figure 3 also shows the detrimental effect of water during the reduction
– pressure is maintained by pure H2 make up phase. The degree of platinum dispersion achieved after reduction on a
dried catalyst is much lower than with a dried, calcined catalyst
– the water is purged from low points and separators
OPERATIONS COMMENTS
• The aim of sulfurization is to temporarily curb the overly high activity of the
VI – SULFURIZATION metals that were formed during the reduction phase. These metals in fact
promote the hydrocarbon HYDROGENOLYSIS reaction (bond breakage in
the presence of hydrogen). The reaction is also called METHANIZATION
since it produces mainly methane and coke which is then deposited on the
catalyst surface.
• Reactor t is lowered to 430°C, sulfurization is begun and continues at
400°C
• DMDS (dimethyl disulfide) breaks down when hydrogen is present to form
the sulfurization agent H2S according to the reaction below:
• DMDS is injected reactor by reactor (3, 1, 2), corresponding to
0.2% mass of sulfur in relation to the catalyst CH3 — S — S —CH3 + 3H2 2H2S + 2CH4
OPERATIONS COMMENTS
The metallic function is temporarily poisoned due to the H2S that was
generated. It sulfurizes the platinum according to the following reversible
reaction for example:
R — Pt + H2S R— Pt — S + H2
Platinum
sulfide
OPERATIONS COMMENTS
• Pressure increase is monitored until operating pressure is reached • The gas produced by the reactions allows pressure to be increased in the
unit
• Flow is increased to nominal rate
• The unit is dried while the chlorine rate is held on the catalyst. Meanwhile,
as the most hydrogenolyzing metallic sites "calm down", sulfur in the H2S
• Drying and sulfur removal phase, chlorinated compound is injected form is eliminated to restore the metallic function to normal activity
• First STAGE at 460°C • The temperature is raised in stages depending on the water and H2S
content of the recycle gas with appropriate injection of the chlorinated
compound
as long as: there is water in the recycle gas > 200 ppm volume
and H2S > 10 ppm volume.
OPERATIONS COMMENTS
• SEVERITY IS ADJUSTED TO GET THE REQUIRED PERFORMANCE • Normal operation of the unit is begun
Oxygen analyser if
second injection.
Steam
SC
TRC TRC TRC
T
FG FG FG
TR
TR TR F
TR Oxygen
TR analyzer
TR TR FRC
TR
Atm. Caustic soda
TR TR PR Air
TR 50%
FRC
F LRC
TR
CATALYTIC REFORMING FRC pH
Semi regenerative Unit F
— Regeneration loop —
D PCD 155 W
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