Showing posts with label reaction. Show all posts
Showing posts with label reaction. Show all posts
Wednesday, April 28, 2010
Vacuum Condensers
Outlet Temperature and Pressure. It is important to have proper subcooling in the vent end of the unit to prevent large amounts of process vapors from going to the vacuum system along with the inerts.
Control. It is necessary to have some over-surface and to have a proper baffling to allow for pressure control during process swings, variable leakage of inerts, etc. One designer adds 50% to the calculated length for the oversurface. The condenser must be considered part of the control system (similar to extra trays in a fractionator to allow for process swings not controlled by conventional instrumentation).
The inerts will “blanket” a portion of the tubes. The blanketed portion has very poor heat transfer. The column pressure is controlled by varying the percentage of the tube surface blanketed. When the desired pressure is exceeded, the vacuum system will suck out more inerts, and lower the percentage of surface blanketed. This will increase cooling and bring the pressure back down to the desired level. The reverse happens if the pressure falls below that desired. This is simply a matter of adjusting the heat transfer coefficient to heat balance the system.
Figure 1 shows typical baffling. The inerts move through the first part of the condenser as directed by the baffles. The inerts then pile up at the outlet end lowering heat transfer as required by the controller. A relatively large section must be covered by more or less stagnant inerts which are sub-cooled before being pulled out as needed. Without proper baffles, the inerts build up in the condensing section and decrease heat transfer until the pressure gets too high. Then the vacuum valve opens wider, pulling process vapor and inerts into the vacuum system. Under these conditions pressure control will be very poor.
Pressure Drop. Baffling must be designed to keep the pressure drop as low as possible. The higher the pressure drop the higher the energy consumption and the harder the job of attaining proper vent end sub-cooling. Pressure drop is lower at the outlet end because of smaller mass flow.
Bypassing. Baffles should prevent bypass of inlet vapor into the vent. This is very important.
Typical Condenser. Figure 1 illustrates an inlet “bathtub” used for low vacuums to limit pressure drop at entrance to exchanger and across first rows of tubes. Note staggered baffle spacing with large spacing at inlet, and the side to side (40% cut) baffles. Enough baffles must be used in the inlet end for minimum tube support. In the last 25% of the outlet end a spacing of 1/10 of a diameter is recommended.
Source: Based on notes provided by Jack Hailer and consultation by Guy Z. Moore while employed at El Paso Products Co.
Wednesday, April 14, 2010
share all about conversion units
All about conversion unit!!!
1. Change Unit


2. Conversion


3. Convert


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1. Change Unit
2. Conversion
3. Convert
BONUS, turbine steam consumption calculator!!
you can download here
Monday, April 12, 2010
Classification of Reactions
There are many ways of classifying chemical reactions. In chemical reaction
engineering probably the most useful scheme is the breakdown according to
the number and types of phases involved, the big division being between the
homogeneous and heterogeneous systems. A reaction is homogeneous if it takes
place in one phase alone. A reaction is heterogeneous if it requires the presence
of at least two phases to proceed at the rate that it does. It is immaterial whether
the reaction takes place in one, two, or more phases; at an interface; or whether
the reactants and products are distributed among the phases or are all contained
within a single phase. All that counts is that at least two phases are necessary
for the reaction to proceed as it does.
Sometimes this classification is not clear-cut as with the large class of biological
reactions, the enzyme-substrate reactions. Here the enzyme acts as a catalyst in
the manufacture of proteins and other products. Since enzymes themselves are
highly complicated large-molecular-weight proteins of colloidal size, 10-100 nm,
enzyme-containing solutions represent a gray region between homogeneous and
heterogeneous systems. Other examples for which the distinction between homogeneous
and heterogeneous systems is not sharp are the very rapid chemical
reactions, such as the burning gas flame. Here large nonhomogeneity in composition
and temperature exist. Strictly speaking, then, we do not have a single phase,
for a phase implies uniform temperature, pressure, and composition throughout.
The answer to the question of how to classify these borderline cases is simple.
It depends on how we choose to treat them, and this in turn depends on which description we think is more useful. Thus, only in the context of a given situation
can we decide how best to treat these borderline cases.

Cutting across this classification is the catalytic reaction whose rate is altered
by materials that are neither reactants nor products. These foreign materials,
called catalysts, need not be present in large amounts. Catalysts act somehow as
go-betweens, either hindering or accelerating the reaction process while being
modified relatively slowly if at all.
Table 1.1 shows the classification of chemical reactions according to our scheme
with a few examples of typical reactions for each type.
engineering probably the most useful scheme is the breakdown according to
the number and types of phases involved, the big division being between the
homogeneous and heterogeneous systems. A reaction is homogeneous if it takes
place in one phase alone. A reaction is heterogeneous if it requires the presence
of at least two phases to proceed at the rate that it does. It is immaterial whether
the reaction takes place in one, two, or more phases; at an interface; or whether
the reactants and products are distributed among the phases or are all contained
within a single phase. All that counts is that at least two phases are necessary
for the reaction to proceed as it does.
Sometimes this classification is not clear-cut as with the large class of biological
reactions, the enzyme-substrate reactions. Here the enzyme acts as a catalyst in
the manufacture of proteins and other products. Since enzymes themselves are
highly complicated large-molecular-weight proteins of colloidal size, 10-100 nm,
enzyme-containing solutions represent a gray region between homogeneous and
heterogeneous systems. Other examples for which the distinction between homogeneous
and heterogeneous systems is not sharp are the very rapid chemical
reactions, such as the burning gas flame. Here large nonhomogeneity in composition
and temperature exist. Strictly speaking, then, we do not have a single phase,
for a phase implies uniform temperature, pressure, and composition throughout.
The answer to the question of how to classify these borderline cases is simple.
It depends on how we choose to treat them, and this in turn depends on which description we think is more useful. Thus, only in the context of a given situation
can we decide how best to treat these borderline cases.
Cutting across this classification is the catalytic reaction whose rate is altered
by materials that are neither reactants nor products. These foreign materials,
called catalysts, need not be present in large amounts. Catalysts act somehow as
go-betweens, either hindering or accelerating the reaction process while being
modified relatively slowly if at all.
Table 1.1 shows the classification of chemical reactions according to our scheme
with a few examples of typical reactions for each type.
Friday, April 9, 2010
Overview of Chemical Reaction Engineering
Every industrial chemical process is designed to produce economically a desired
product from a variety of starting materials through a succession of treatment
steps. Figure 1.1 shows a typical situation. The raw materials undergo a number
of physical treatment steps to put them in the form in which they can be reacted
chemically. Then they pass through the reactor. The products of the reaction
must then undergo further physical treatment-separations, purifications, etc.-
for the final desired product to be obtained.
Design of equipment for the physical treatment steps is studied in the unit
operations. In this book we are concerned with the chemical treatment step of
a process. Economically this may be an inconsequential unit, perhaps a simple
mixing tank. Frequently, however, the chemical treatment step is the heart of
the process, the thing that makes or breaks the process economically.
Design of the reactor is no routine matter, and many alternatives can be
proposed for a process. In searching for the optimum it is not just the cost of
the reactor that must be minimized. One design may have low reactor cost, but
the materials leaving the unit may be such that their treatment requires a much
higher cost than alternative designs. Hence, the economics of the overall process
must be considered.
Reactor design uses information, knowledge, and experience from a variety
of areas-thermodynamics, chemical kinetics, fluid mechanics, heat transfer,
mass transfer, and economics. Chemical reaction engineering is the synthesis of
all these factors with the aim of properly designing a chemical reactor.
To find what a reactor is able to do we need to know the kinetics, the contacting
pattern and the performance equation. We show this schematically in Fig. 1.2.

Figure 1.1 Typical chemical process.

Figure 1.2 Information needed to predict what a reactor can do.
Much of this book deals with finding the expression to relate input to output
for various kinetics and various contacting patterns, or
output = f [input, kinetics, contacting]
This is called the performance equation. Why is this important? Because with
this expression we can compare different designs and conditions, find which is
best, and then scale up to larger units.
source: Octave Levenspiel
product from a variety of starting materials through a succession of treatment
steps. Figure 1.1 shows a typical situation. The raw materials undergo a number
of physical treatment steps to put them in the form in which they can be reacted
chemically. Then they pass through the reactor. The products of the reaction
must then undergo further physical treatment-separations, purifications, etc.-
for the final desired product to be obtained.
Design of equipment for the physical treatment steps is studied in the unit
operations. In this book we are concerned with the chemical treatment step of
a process. Economically this may be an inconsequential unit, perhaps a simple
mixing tank. Frequently, however, the chemical treatment step is the heart of
the process, the thing that makes or breaks the process economically.
Design of the reactor is no routine matter, and many alternatives can be
proposed for a process. In searching for the optimum it is not just the cost of
the reactor that must be minimized. One design may have low reactor cost, but
the materials leaving the unit may be such that their treatment requires a much
higher cost than alternative designs. Hence, the economics of the overall process
must be considered.
Reactor design uses information, knowledge, and experience from a variety
of areas-thermodynamics, chemical kinetics, fluid mechanics, heat transfer,
mass transfer, and economics. Chemical reaction engineering is the synthesis of
all these factors with the aim of properly designing a chemical reactor.
To find what a reactor is able to do we need to know the kinetics, the contacting
pattern and the performance equation. We show this schematically in Fig. 1.2.
Figure 1.1 Typical chemical process.
Figure 1.2 Information needed to predict what a reactor can do.
Much of this book deals with finding the expression to relate input to output
for various kinetics and various contacting patterns, or
output = f [input, kinetics, contacting]
This is called the performance equation. Why is this important? Because with
this expression we can compare different designs and conditions, find which is
best, and then scale up to larger units.
source: Octave Levenspiel
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