Lecture 08 - Heuristics For Process Synthesis (Part 3)
Lecture 08 - Heuristics For Process Synthesis (Part 3)
LECTURE 08
Heuristics for Process
Synthesis (Part 3)
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Introduction
Once the input-output structure of the process
has been decided, the reactor structure of the
process can then be developed.
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Reaction Data
Data on reaction thermodynamics and kinetics
must be available before proceeding to this stage
of process synthesis and development.
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Reaction Data
Data on reaction thermodynamics and kinetics
must be available before proceeding to this
stage of process synthesis and development.
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Reaction Data
Reaction Data
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Batch Reactor
The reactants are charged at the beginning of
the operation. The contents are subjected to
perfect mixing for a certain period, after which
the products are discharged.
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Plug-Flow Reactor
The raw materials are continuously fed and the
products are continuously withdrawn from opposite
ends of a pipe. The concentrations vary along the
length of the pipe.
Real Reactors
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Real Reactors
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Real Reactors
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A→B r = kCAa
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A→B r = kCAa
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A → B (desired) r1 = k1CAa1
A → C (undesired) r2 = k2CAa2
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A → B (desired) r1 = k1CAa1
A → C (undesired) r2 = k2CAa2
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Feed Concentrations
Single Irreversible Reactions
When dealing with a single irreversible
reaction, the goal is usually to minimize
reactor capital cost by minimizing reactor
volume for a given conversion.
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Feed Concentrations
Single Irreversible Reactions
The usual choice of excess reactant is to
eliminate the component that is more
difficult to separate in the downstream
system. Economics and safety are also
considered (i.e., if the limiting reactant is
expensive and/or hazardous).
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Feed Concentrations
Single Reversible Reactions
An excess of one feed can be used to shift
the equilibrium towards the forward
reaction, at the expense of higher capital
due to higher equipment capacities.
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Feed Concentrations
Multiple Reactions
When dealing with multiple reactions, the goal is
usually to maximize selectivity by minimizing by-
product formation for a given conversion.
A + B → C (desired) r1 = k1CAa1CBb1
A + B → D (undesired) r2 = k2CAa2CBb2
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Feed Concentrations
Multiple Reactions
When dealing with multiple reactions, the goal is
usually to maximize selectivity by minimizing by-
product formation for a given conversion.
A + B → C (desired) r1 = k1CAa1CBb1
A + B → D (undesired) r2 = k2CAa2CBb2
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Feed Concentrations
Process Heuristics
1. Higher concentrations in feed will lead to
higher reaction rates, which may be
dangerous for highly exothermic reactions.
An excess of the other feed or the addition of
an inert material reduces this possibility.
Feed Concentrations
Process Heuristics
3. Provide purge streams as exits for feed
impurities or for those formed as products of
irreversible side reactions ONLY when these
species are in trace quantities or will require
difficult separation. Lighter species leave in
vapor purge streams, and heavier specie exit
in liquid purge streams.
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Feed Concentrations
Process Heuristics
5. By-products produced in reversible reactions
and in small quantities are usually just
recycled to extinction.
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Feed Concentrations
Example: What should be the limiting and excess
reactants for the formaldehyde production via
partial oxidation of methanol, methanol or
oxygen?
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Reaction Temperature
When dealing with a single irreversible
reaction, the goal is usually to minimize
reactor capital cost by minimizing reactor
volume for a given conversion.
Example: What temperature is the better choice for the
following irreversible reaction, high or low?
A→B r = kCAa
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Reaction Temperature
When dealing with a single irreversible
reaction, the goal is usually to minimize
reactor capital cost by minimizing reactor
volume for a given conversion.
Example: What temperature is the better choice for the
following irreversible reaction, high or low?
A→B r = kCAa
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Reaction Temperature
When dealing with multiple irreversible
reactions, the goal is usually to maximize
selectivity by minimizing by-product formation
for a given conversion.
A → B (desired) r1 = k1CAa1
A → C (undesired) r2 = k2CAa2
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Reaction Temperature
When dealing with multiple irreversible
reactions, the goal is usually to maximize
selectivity by minimizing by-product formation
for a given conversion.
A → B (desired) r1 = k1CAa1
A → C (undesired) r2 = k2CAa2
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Reaction Temperature
For reversible reactions, consider the heat of
reaction in choosing the reaction temperature
(Le Chatelier’s principle).
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Reaction Temperature
Process Heuristics
1. If heat of reaction is small, a small change of
temperature across the reactor may be
acceptable and heating/cooling can be
avoided. Operate in adiabatic mode.
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Reaction Temperature
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Reaction Temperature
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Feed Concentrations
Process Heuristics
4. Operating at very high temperatures will lead
to higher reactor cost. Operating conditions
above 400°C must be justified and must have
proper selection for materials of
construction.
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Feed Concentrations
Process Heuristics
5. The objective in heating or cooling reactor
contents is to achieve uniform temperature
throughout the unit and eliminate hot/cold
spots.
• Indirect heat transfer
• Direct heat transfer
• Interstage heating/cooling
• Heat-exchange devices as reactors
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Reaction Temperature
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Reaction Temperature
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Reaction Temperature
Example: What temperature is the better choice
for the formaldehyde production via partial
oxidation of methanol, high or low?
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Reaction Temperature
Example: Should formaldehyde production via
partial oxidation of methanol be performed in
an adiabatic reactor or an isothermal reactor?
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Reaction Pressure
Reactor pressure can shift the equilibrium of
gas-phase reversible reactions based on the
change on the number of moles (∆N).
Reaction Pressure
Example: What pressure is the better choice for
the formaldehyde production via partial oxidation
of methanol, high or low?
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Answer: PFR. At the inlet of the PFR, the main reaction rate is
heavily promoted by high methanol partial pressure and the
side reaction rate is heavily inhibited by low formaldehyde
partial pressure.
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Feed Concentrations
Example: What should be the limiting reactant for
the formaldehyde production via partial oxidation
of methanol, methanol or oxygen?
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Reaction Temperature
Example: What temperature is the better choice
for the formaldehyde production via partial
oxidation of methanol, high or low?
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Reaction Temperature
Example: Should formaldehyde production via
partial oxidation of methanol be performed in
an adiabatic reactor or an isothermal reactor?
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Reaction Pressure
Example: What pressure is the better choice for
the formaldehyde production via partial oxidation
of methanol, high or low?
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Excess Air
Min The air flowrate that will yield a methanol-air
mixture at LEL. Below this minimum flowrate, the
gas mixture becomes explosive.
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Temperature
Min 234°C
Below this temperature, HP steam can be used as
heating medium instead of fuel gas. The use of a
shell-and-tube heat exchanger instead of a furnace
will change the entire calculation and will not be
explored due to time constraints.
Max 400°C
The thermal stability of Dowtherm A, the heat
transfer fluid circulated to maintain the reactor
temperature, is only up to 400°C.
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Pressure
Min 0 kPag
Lowest possible pressure inside reactor.
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Conversion
Since the range of residence time cannot be defined,
establish the limits on conversion instead.
Max ~98%
The formalin solution can have at most 1 wt%
unreacted methanol based on the product
specifications. At this conversion, methanol recycle
rate is zero.
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